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A Clinical Case Presentation
The Power of Change: A Case of a
Adolescent with Multiple Medical
Condition
Alejandro E. Legarda III MD
First Year Resident
DFCM
Objectives
• To present an adolescent with hypertension and obesity
and its correlation to Metabolic syndrome and PCOS
• To discuss the differential diagnosis for high BP in the
young
• To discuss the approach to management of adolescent
with hypertension, obesity and the diagnose syndromes
• To present short-term and long-term wellness plan
appropriate for the patient's condition
Patient Profile
EJ
13 years old
Single
Roman Catholic
Incoming 3rd year high school student
Chief Complaint
ELEVATED BLOOD PRESSURE
Clinical History
Five years
prior to
consult
(2007)
• The patient was then eight years old
and sought a consult due to her re-
occurring erythematous vesicular
lesions.
• Upon consultation, she was diagnosed
with Post-streptococcal
glomerulonephritis. The patients was
admitted in the hospital for a week due
to this condition.
• Patient was documented to suffer from
hypertension. Nifedipine was prescribed
to control and manage her
hypertension.
After hospitalization, patient felt well again. No follow-up consult was
recommended to the patient.
Three years
prior to
consult
(2009)
• The patient started gaining
weight as food intake severely
increased.
• Patient’s BP was taken annually
in school and showed elevated
blood pressure.
• The increased blood pressure
readings was simply ignored by
the patient and her parents,
thus resulting in progressive,
uncontrolled weight gain.
Clinical History
Two weeks prior to
consult
• Patient sought consultation at the UP-PGH
Dermatological Department for her vesicular
lesions.
• Patient featured an incidental finding of 160-90
blood pressure reading.
• Assessment reveals:
Acne vulgaris with etiology related to PCOS
Hypertension secondary to (1) PCOS (2)
Cushing’s Syndrome (3) Insect bite hyper
sensitivity reaction
Patient was given:
• Amlodipine (5mg./tab) OD
• Benzoyl Peroxide gel OD
• Tretinoin cream for the face
• Cloxacilin (500mg./tab) for 7 days
• Mupirocin Bethamethasone ointment ITD
• Sunscreen
• mild soap
Clinical History
Patient was referred to Pedia adolescent, hence the consult.
Clinical History
 At Consult (March 26, 2012)
 Patient was seen at the
Pedia Adolescent Clinic
Review of Systems
(+) polyuria
(+) polydipsia
(-) rashes
(-) epistaxis
(-) gum bleeding
(-) neck pain
(-) dysphagia
(-) chest pain
(-) orthopnea
(-) dyspnea on exertion
(-) orthopnea
(-) edema
(-) neck pain
(-) abdominal pain
(-) constipation
(-) diarrhea
(-) urgency
(-) frequency
(-) dysuria
(-) nocturia
(-) hematuria
(-) heat intolerance
(-) jaundice
Past Medical History
(-) Asthma
(-) Allergy
(-) Pulmonary Tuberculosis
(-) Bronchial asthma
No Accident and injury
Hospitalizations:
Admitted for (+) PSGN (2007) and Dengue Fever (2009)
Surgeries:
There was no previous surgery
Medications:
Co-amoxiclav for her recurrent skin infections
OB/GYNE History
Menarche: January 2011
Irregular flow occurring only 3x since her
menarche
Lasting 4-5 days, Pads 2-4 a day
No dysmenorrhea
No sexual contact
Birth and Maternal History
Patient was born full-term via spontaneous
vaginal delivery at a local hospital delivered by
an obstetrician with no known feto-maternal
complications.
NUTRITIONAL HISTORY
Patient was breastfed for 3 months and then shifted
to bottle feeding of Bona milk every 3 to 4 hours
starting at 4 months old up to 12 months old.
Complementary feeding was started at 6 months
old.
Patient would skip breakfast but would have 2
snacks before a heavy lunch. She would have 2 heavy
meriendas, e.g.,2 hamburgers/hotdogs or cups of ice
cream .Most of the food she eats are either fried or
salty and plenty of desserts. She loves to drink cola.
Immunization History
Childhood Vaccinations
Bacillus Calmette-Guerin (BCG), one dose
Hepatitis B vaccine, three doses
Diptheria Pertussis Tetatnus (DPT), three doses
Oral Polio Vaccine, thress doses
Measles, one dose
FAMILY GENOGRAM
I
II
III
Jorgo Family
March 26, 2012
Hypertension
Accident
Overweight
Diabetes
76 80
68 75
56 54
32
50 46
52 48
19 18 15 13
Elaisa
JJMJ
EJ
Personal and Social History
Home:
- lives with parents and four siblings in Imus, Cavite
-good relationship with parents and siblings
Education:
-Incoming third-year high school student
-With above-average grades
- has close set of friends in school
Activities:
-Favorite past time– eating
-Loves eating street foods and junk foods
-Spends most of her free time in front of the TV or
computer
-Not involved in any outdoor activities such as sports
Personal and Social History
Drugs:
-No history of cigarette or alcohol use
-Denies use or history of use of illicit drugs
Sexual:
-Does not showcase any consciousness with body weight and
shape
-Patient has not attempted to change her appearance
-Currently no relationship with the opposite sex
Suicidal Tendencies:
-Patient exhibits no signs or episodes of depression or suicidal
ideation
Safety:
-Patient together with her family lives in a peaceful and orderly
community with minimum crime rate
- uses public transportation to commute
-Not a member of a gang or sorority
Physical Examination
General Survey:
Awake, alert, coherent, in pain, not in cardio-respiratory distress
(-) muscle wasting
(-) moon face
(-) proximal muscle weakness
(-) buffalo hump
Vital Signs:
Blood Pressure: 150/90(>99th percentile)
Heart Rate: 75 beats/minute
Respiratory Rate: 18 breaths/minute
Temperature: 36.8 C
Physical Examination
Anthropometrics:
Height: 157 cm
Weight: 96.5 kg
Body Mass Index: 40.7 kg/m2
(Z score: 2.58)
Abdominal Circumference 102cm
Physical Examination
Head and Neck:
Anicteric sclerae, pink conjunctivae,
pupils 2-3mm OU reactive to light,
(+) Short leg length
(+) Acanthosis nigricans,
(-) masses, (-) cervical lymphadenopathy,
(-) anterior neck mass
(-) tonsillopharyngealcongestion,
(-) neck vein engorgement, (-)ear discharge
Physical Examination
Chest and Lungs:
Equal chest expansion, no deformities,
no lesions, clear breath sounds,
(-) crackles/rales/wheezes
Heart:
Adynamic precordium, distinct heart sounds,
apex beat at 5th intercostal space left midclavicular line,
regular rate and rhythm, no murmurs
Physical Examination
Abdomen:
flabby
(+) Striae lower abodomen
no deformities
no lesions
Soft normoactive bowel sounds
(-)masses or tenderness
liver span 8 cm right midclavicular line
intact Traube’s space
no costo-vertebral angle tenderness
Physical Examination
Extremities
pink nailbeds
full and equal pulses
no cyanosis/clubbing/ edema
no crepitations
no limitation of passive and active motion
on both upper extremities
(-) shooting pain on straight leg raise of
both lower extremities
(-) limitation of motion due to pain
no crepitations on hips, knees or ankles
no joint swelling or deformities
(-) Pain on active leg raise of both
lower extremities
Physical Examination
Neuro Exam
Cranial Nerve (CN) Examination
CN I –intact gross olfaction
CN II –pupils 2-3 mm OU briskly reactive to light
CN III,IV,VI –full range of extraocular muscle movement
CN V –brisk corneals, good masseter tone,
CN VII –no facial asymmetry, no altered taste
CN VIII –intact gross hearing, no lateralization on Weber Test
CN IX –no altered taste, can swallow
CN X –can swallow
CN XI –good symmetrical shrug
CN XII –can protrude tongue, no deviation
Physical Examination
Sensory
Pain: Intact on all dermatomes
Light Touch: Intact on all dermatomes
Vibratory: Intact on all dermatomes
Motor
Normal Gait
Good muscle tone, no atrophy, no limb size discrepancy
Full motor strength on both upper extremities
Tanner Stage 3
External genitalia with dark, coarse
curly hair spreads over mons pubis
Elevation of Breast contour; areolae enlarged
Salient Features of the Case
SALIENT FEATURES OF THE CASE
A 13-year old female
Chief complaint of elevated blood pressure
History of hypertension ,DM and Obesity
Previous history of renal disease (+) poluyuria, (+)
polyphaga.
Amenorrhea
Obesity
Anthropometrics: Height: 157 cm, Weight: 96.5 kg, Body
Mass Index: 40.7 kg/m2 (Z score: 2.58),
(+) Short neck length
(+) Acanthosis nigricans nape area,
Flabby abdomen with (+) Striae
Initial Impression
Hypertension, Stage II-- etiology to be
determined
Acne Vulgaris probably secondary to PCOS
DM suspect
Obese, Type 2
Amenorrhea secondary to PCOS
Management
Diagnostics:
Complete Blood Count (CBC)
Plasma sodium, potassium and calcium
BUN, Creatinine
Fasting plasma glucose
Lipid profile
Urinalysis
Whole AB ultrasound
Chest X--ray
ECG
TSH, FT4
Therapeutics
Continue the following medications:
Cloxacillin 500 for 7 days
Tretnoin Cream for the face
Mupirocine Betamethasone ointment, TID
Sun screen use
Mild soap use
Start Amlodipine 5mg once a day
Approach to Hypertension
European Society of Hypertension
The study mentioned childhood BP has been shown to
track into adulthood
Unlike adults, the diagnostic criteria for elevated BP in
children are based on the concept that BP in children
increases with age and body size, making it impossible to
utilize a single BP level to define hypertension.
The recommended method is auscultatory.
Use K1 for systolic BP and K5 for diastolic B.
If the oscillometric method is used, the monitor needs to be validated
and if hypertension is detected by the oscillometric method, it needs to
be confirmed using the auscultatory method.
The Use the appropriate cuff size according to arm width (40% of the
arm circumference) and length (4_8 cm, 6_12 cm, 9_18 cm, 10_24 cm,
to cover 80–100% of the individual’s arm circumference).
Specific recommendations for office BP
measurement in children and adolescents
Blood Pressure for Girls by Age and Height Percentiles
Systolic and diastolic ambulatory blood pressure
(systolic/diastolic) values for clinical use
Task Force for Blood Pressure in Children, the Fourth Report on
the Diagnosis, Evaluation, and Treatment of High Blood
Pressure in Children and Adolescents
The normal BP in children is defined as SBP and DBP less than
90th percentile for age, sex and height.
Hypertension is defined as SBP and/or DBP persistently 95th
percentile or more, measured on at least three separate occasions
with the auscultatory method.
Rule out White-coat (or isolated office) and masked (or
isolated ambulatory) hypertensions
Definition and Classification of Hypertension in Children and
Adolescents
Diagnostic Algorithm of Hypertension
FAMILY HISTORY
Hypertension
Cardiovascular and cerebrovascular disease
Diabetes mellitus
Dyslipidemia
Obesity
Hereditary renal disease (Policystic kidney disease)
Hereditary endocrine disease (pheochromocytoma
glucocorticoid-remediable aldosteronism, multiple
endocrine neoplasia type 2, von Hippel–Lindau)
Syndromes associated with hypertension (neurofibromatosis)
Clinical Data To Note
Clinical Data To Note
PERINATAL HISTORY
Birth weight, gestational age, oligohydramnios,
anoxia, umbilical artery catheterization
PREVIOUS HISTORY
Hypertension
Urinary tract infection, renal or urological disease
Cardiac, endocrine (including diabetes) or neurological
disease
Growth retardation
Symptoms suggestive of secondary hypertension
Dysuria, thirst/polyuria, nocturia, hematuria
Edema, weight loss, failure to thrive
Palpitations, sweating, fever, pallor, flushing
Cold extremities, intermittent claudication
Virilization, primary amenorrhea and male pseudohermaphroditism
Symptoms suggestive of target organ damage
Headache, epistaxis, vertigo, visual impairment
Facial palsy, fits, strokes
Dyspnea
Clinical Data To Note
Sleep history:
Snoring
apnea,
daytime somnolence
Risk factor history:
Physical exercise, dietary habits
Smoking, alcohol
Drug intake:
Anti-hypertensives
Steroids, cyclosporine
tacrolimus or otherTri-cyclic anti-depressants
atypical antipsychotics
decongestants
Oral contraceptives
illegal drugs
Pregnancy
Physical Examination To Note
Height
Weight
Body mass index
External features of syndromes/conditions associated with
hypertension
Neurofibromatosis
Klippel–Trenaunay–Weber
Feuerstein–Mims
Von Hippel–Lindau
Multiple endocrine neoplasia
Pseudoxanthoma elasticum
Turner,
William
Marfan
Cushing
Hyperthyroidism,
Lupus
Vasculitis
Congenital adrenal hyperplasia
Data to record:
Physical Examination
Data to Record
Cardiovascular examination
Pulse and BP measurement in both arms and legs
Bruits/murmurs – heart, abdomen, flanks, back,
neck, head
Signs of left ventricular hypertrophy or cardiac failure
Abdomen
Masses – Wilms, neuroblastoma, pheochromocytoma, autosomal
dominant and recessive polycystic kidney disease, multicystic kidney
displasia, obstructive uropathy
Hepatosplenomegaly – autosomal recessive polycystic kidney disease
Neurological examination
Fundoscopy for hypertensive changes and retinal
amartoma (von Hippel–Lindau)
Evidence of VIII nerve palsy
Other neurological defects including stroke
Indicators on Physical Exam of Etiology of Hypertension in a Child
Thyromegaly Hyperthyroidism
Acne, hirsutism, striae Cushing syndrome, anabolic steroid abuse
Cafe´-au-lait spots Neurofibromatosis
Adenoma sebaceum Tuberous sclerosis
Malar rash Systemic lupus erythematosus
Acanthrosis nigricans Type 2 diabetes
Chest widely spaced nipples Turner syndrome
Heart murmur Coarctation of the aorta
Friction rub Systemic lupus erythematosus (pericarditis),
Abdomen Mass Wilms tumor, neuroblastoma,
pheochromocytoma
Epigastric/flank bruit Renal artery stenosis
Palpable kidneys Polycystic kidney disease, hydronephrosis,
multicysticdysplastic kidney
Genitalia Ambiguous/virilization Adrenal hyperplasia
Extremities Joint swelling Systemic lupus erythematosus, collagen vascular
ds
Muscle weakness Hyperaldosteronism, Liddle syndrome
Patient PE Presentation
Significant Anthropometrics:
Height: 157 cm
Weight: 96.5 kg,
Body Mass Index: 40.7 kg/m2 (Z score: 2.58)
(+) Short neck length
(+) Acanthosis nigricans nape area
Flabby abdomen with (+) Striae
(+) Acne
Other details were none pertinent
Target Organ Damage To Note
Heart
Blood Vessels
Kidney
Neuro
Fundoscopy
Heart
Left Ventricular Hyperthrophy (LVH) remains to date the most
thoroughly documented form of end-organ damage caused by
hypertension in children and adolescents.
Blood Vessels
Morphological changes of the arterial wall, thickening of the intima-media
complex.
Children with familial hypercholesterolemia have higher IMT
Overweight and obesity are associated with increased IMT in children with or
without essential hypertension.
Kidney
Hypertension-related renal damage is based
on a reduced renal function or an elevated
UAE. Proteinuria is a marker of glomerular
damage in primary and secondary
glomerulopathies. An indication for BP-
lowering interventions.
Microalbuminuria (20–300mg/g creatinine,
2–30 mg/mmol creatinine, 30–300 mg/day,
20–200mg/min) has been shown to predict the
development of diabetic nephropathy .
Overt proteinuria (>300 mg/day) indicates
the existence of established renal parenchymal
damage.
Neuro and Fundoscopy
Cerebral seizures, stroke, visual
impairment and retinal vascular changes are
complications associated with severe
hypertension.
Fundoscopy was also done in because in
a study of 97 children and adolescents with
essential hypertension, found that 51%
displayed retinal abnormalities, as detected
from direct ophthalmoscopy.
Obesity and Hypertension
Using the 2000 CDC growth charts, at risk of overweight
for ages 2 to 20 years overweight is defined as a Body
Mass Index (BMI)-for-age between the 85th and the 95th
percentiles.
Overweight in children is defined as a BMI-for-age at or
above the 95th percentile on the charts.
BMI is weight in kilograms divided by height in meters
squared (kg/m2).
BMI is used differently to define overweight in children
and adolescents than it is in adults. In children and
adolescents, BMI changes with age and gender.
Obesity and Hypertension
Overweight children and adolescents are at
increased risk for various chronic diseases
in later life.
The psychosocial consequences of
overweight are significant. Overweight in
children has been linked to social
discrimination, a negative self-image in
adolescence that often persists into
adulthood, parental neglect, and behavioral
and learning problems.
Obesity and Hypertension
Being overweight is probably the most
important of the conditions associated with
elevated BP in childhood and accounts for
more than half the risk for developing
hypertension.
Adiposity is the most powerful risk factor
for higher BP.
Waist circumference (abdominal obesity)
has been shown to play a role.
Dietary habits like high salt intake, have
been implicated as factors favoring higher BP
values.
Obesity and Hypertension
The CDC mentions the Common Medical
Consequences of Overweight (Dietz,
1998)
hyperlipidemia
glucose intolerance
hepatic steatosis
cholelithiasis
sleep apnea
Obesity
hypoventilation syndrome
hypertension
a variety of orthopedic complications
Laboratory Investigations
Full blood count
Plasma sodium, potassium and
calcium, urea, creatinine
Fasting plasma glucose
Serum lipids (cholesterol, LDL
cholesterol, HDL
cholesterol)
Fasting serum triglycerides
Urinalysis plus quantitative
measurement of
microalbuminuria
and proteinuria
Renal ultrasound
Chest Xray, ECG and 2-D
echocardiography
Routine tests that have to be performed in all
hypertensive children
 Recommended additional
screening tests
 Plasma renin activity, plasma aldosterone concentration
 Urine and plasma catecholamines or metanephrines
 Tc99 dimercaptosuccı´nic acid scan
 Urinary free cortisol
 More sophisticated tests that should await results of
 above screening
 Color Doppler ultrasonography
 Captopril primed isotope studies
 Renal vein renin measurements
 Renal angiography
 I123 metaiodobenzylguanidine scanning
 Computed tomography/ Magnetic resonance imaging
 Urine steroid analyses and more complex endocrine
 investigations
 Molecular genetic studies (Apparent mineralocorticoid
 excess, Liddle’s syndrome, etc)
SECONDARY HYPERTENSION
Sustained hypertension can be
classified as secondary when a
specific cause can be found, then
it can be corrected with specific
intervention.
There should be work-up should
be done if hypertension .
Diagnosis of Secondary Causes of
Hypertension
MY MANAGEMENT
Diagnostic Examinations
Laboratory Plan:
Complete blood count
Plasma sodium, potassium and calcium,
BUN, Crea
Fasting plasma glucose
Lipid Profile
Urinalysis
Whole AB ultrasound
Chest Xray, ECG
TSH, FT4
APPROACH TO MANAGEMENT
Non pharmacologic Strategy Recommendations:
GOALS:
BMI<85th percentile: Maintain BMI to prevent becoming
overweight
BMI 85–95th percentile: Weight maintenance (younger children)
or gradual weight loss in adolescents
To reduce BMI to <85th percentile
BMI>95th percentile: Gradual weight loss (1–2 kg/
month) to achieve value <85th percentile
GENERAL RECOMMENDATIONS
Moderate to vigorous physical aerobic activity--40 min, 3–5
days/week and avoid more than 2 hours daily of sedentary
activities
Avoid intake of excess sugar, excess soft drinks, saturated fat
and salt and recommend fruits, vegetables and grain products
Implement the behavioural changes (physical activity and diet)
tailored to individual and family characteristics
Involve the parents/family as partners in the behavioural
change process
Provide educational support and materials
Establish realistic goals
Develop a health-promoting reward system
Competitive sports participation should be limited
only in the presence of uncontrolled stage 2 hypertension
For my patient…
A. Counseling and Implement Behavioural Change
1.CEA(Catharsis Education Action): Patient
2.Motivational Interviewing- Pre Contemplation stage
3. CEA(Catharsis Education Action): : Parents
Counseling and Implement
Behavior Change: CEA Patient
Patient was not so much concerned of her
weight.
She doesn’t know the risk and the health
issues regarding hypertension.
She was not aware why she came to PGH for
consult and really wanted to go home.
She was also not aware her that being
overweight has some health risks as well.
Use of Motivational Intervierwing
Transtheoretical Model, "process involving progress through a series of
stages:"
 Precontemplation (Not Ready)-"People are not intending to take action
in the foreseeable future, and can be unaware that their behaviour is
problematic.”
 Contemplation (Getting Ready)-"People are beginning to recognize that
their behaviour is problematic, and start to look at the pros and cons of their
continued actions.“
 Preparation (Ready)-"People are intending to take action in the immediate
future, and may begin taking small steps toward behaviour change.“
 Action – "People have made specific overt modifications in modifying their
problem behaviour or in acquiring new healthy behaviours.“
 Maintenance – "People have been able to sustain action for awhile and are
working to prevent relapse."
Use of Motivational
Intervierwing
Motivational Interviewing- Pre Contemplation stage
Patient was on pre -contemplation stage at that time and I
was hoping to make her aware and give her insight to bring
her to the stage where she can contemplate.
When I asked about her hypertension, she said she knew
had it for years but no one told her about the dangers.
B. Counseling and Implement
Behavior Change
3. CEA: Parents
The parents are also unaware of the risk of hypertension and
the eating habits and lifestyle that increase her obesity.
They couldn’t believe that this would happen at her age.
The whole family is at risk since everyone except the wife is
obese.
My Management Plan for the
Patient…
Non-pharmacologic strategies
A. Counseling and Behavior Change- Done
B. I advised the patient to have Regular BP monitoring at home
C. Physical Activity: I mentioned to the patient to start to lessen
sedentary activities and start to walk more around the subdivision and
play with pets. A Exercise program was not done yet as I want for the
patient to reach the preparation/action
D. Eating Habits: Change of eating was advised. The Patient love to
skip breakfast and lessen snack intake.
E. A Diet Program: I was planning to put the patient into a low
Energy Diet of 2000kcal C350 P75 F 35 from a 3022kcal diet on the
next follow up
Approach to Medical
Management on Hypertension
Pharmacologic/Therapeutic Strategies
Aside from the non-pharamacologic strategies, I had a dilemma
on how will I use therapeutic strategies for my patient
EVIDENCE FOR THERAPEUTIC
MANAGEMENT
Reduce mortality and sequelea in life-threateningconditions
Reduce left ventricular hypertrophy
Reduce urinary albumin excretion
Reduce rate of progression to end-stage renal disease
Approach to Medical
Management on Hypertension
Therapeutic management of hypertension
Indications for Antihypertensive Drug Therapy in Children Symptomatic Hypertension
Secondary hypertension
Hypertensive target-organ damage
Diabetes (types 1 and 2)
Persistent hypertension despite non-pharmacologic
measures
>99 percentile BMI
Approach to Medical Management
on Hypertension
Therapeutic Management
Treating Hypertension with drugs are most indicated in end organ
damage of the Heart and Kidney/Renal
Effect to Organ Damage:
In the Heart, Regression of LVH was reported in three children with
essential hypertension receiving enalapril, in 19 children with primary
and secondary hypertension treated with ramipril for 6 months, and in
65 children with chronic kidney disease (CKD) stage 2–4 receiving
ramipril for up to 2 years.
In Renal:
the Effect of Strict Blood Pressure Control and ACE Inhibition on
Progression of Chronic Renal Failure in Pediatric Patients (ESCAPE) trial,
which has shown efficient BP and proteinuria reduction for the ACE
inhibitor ramipril in 352 children with CKD
Approach to Medical
Management on Hypertension
Monotherapy
Choice of anti-hypertensive agents ACEIs
Angiotensin receptor antagonists (ARBs)
Calcium antagonists
Beta-blockers
Diuretics
Combination therapy
In children with renal disease, monotherapy is often not sufficient to
achieve adequate BP control. Therefore, early combination therapy is
required. The best choices of antihypertensive drug combinations are
those recommended in the ESH/ESC 2007 Guidelines .
Clinical conditions for which specific
antihypertensive drug classes are
recommended or contraindicated
My Therapeutic Management
For our patient, she was
given a monotherapy of
Amlopidine, 5mg./tab
once daily.
Initial Management summary
 Diagnostic Examinations
 Laboratory Plan:
 Complete blood count
 Plasma sodium, potassium and calcium,
 BUN, Crea
 Fasting plasma glucose
 Lipid Profile
 Urinalysis
 Whole AB ultrasound
 Chest Xray, ECG
 TSH, FT4
Initial Management summary
 Non-pharmacologic strategies
 Counseling and Behavior Change- Done
 B. I advised the patient to have Regular BP monitoring at home
 C. Physical Activity: I mentioned to the patient to start to lessen
sedentary activities and start to walk more around the subdivision and
play with pets. A Exercise program was not done yet as I want for the
patient to reach the preparation/action
 D. Eating Habits: Change of eating was advised. The Patient love to
skip breakfast and lessen snack intake.
 E. A Diet Program: I was planning to put the patient into a low
Energy Diet of 2000kcal C350 P75 F 35 from a 3022kcal diet on the
next follow up
Initial Management summary
Medical Theraphy
 For our patient, she was given a
monotherapy of Amlopidine, 5mg./tab once
daily.
1st Follow-up April 2012
Maintained BP 150/90…no decrease in BP despite
of Amlodipine 5mg tablet.
Started to jog for several minutes around the
house and roam around the area with her dog.
Lessened her calorie intake thanks to the parents
modifying the food menu at home. Parents started
to prepare healthier food with less salt content.
Parents have been very supportive.
Siblings stopped eating with the patient for snacks
and joined the patient in jogging as well.
One of her sibling, who still was a bad influence to
her was transferred to their grandmother’s house.
1st Follow-up April 2012
 1st Follow-up April 2012
Results
 Hgb:139, Hct 0.432, Plt 356
WBC 8.7
 Urinalysis : Dark yellow,
1.030, RBC 0-2, WBC 3-4 EC
3+ Sugar (-) Albumin (-)
 CXR: Normal Chest Findings
 Thyriod FT4- 20.6, Free T3-
5.5, TSH IRM 6.1
 Glucose 6.4, BUN 3.30, Crea
45.5, Chole 5.0, Trigly 5.01
HDL 0.98, LDL 1.74, AST 38,
ALT 46, Albumin 42 Calcium
2.44, Na- 138, K 4.8
 ECG- Sinus Rhythm, Within
Normal Limits
 Whole Ab Ultrasound: normal
 With the current labs results, I
was able to rule out many
etiology of hypertension
including the secondary ones
however there was elevation in
Triglyceride and there was
Impaired Fasting Glucose
1st Follow-up April 2012
 Previous Salient Features…
SALIENT FEATURES OF THE
CASE
13-year old female
Chief complaint of elevated
blood pressure
History of hypertension ,DM and
Obesity
Previous history of renal disease
(+) poluyuria, (+) polyphaga.
Amenorrhea
Obesity
(+) Short neck length
(+) Acanthosis nigricans nape
area,
(+) Striae
New Finding from the
Diagnostics
Impaired Fasting
Glucose
Elevated Triglyceride
Ruled out
Cardiovascular, Renal
and some secondary
etiology
1st Follow-up April 2012
 Hypertension stage II
secondary to
1) Obesity
2) Metabolic Syndrome
 T/c PCOS sedondary to
Metabolic Syndrome
 Hyperlipidemia
 Impaired Fasting Glucose
METABOLIC SYNDROME
 Group of characteristics:
 Most expert groups define metabolic syndrome as the presence of three or
more of the following characteristics in a person:
 Obesity, especially in the abdominal area
 (defined by some groups as a waist size greater than 94 to 102 cm (38 to 41
in) in men or greater than 80 cm (32 in) in women)
 Impaired fasting glucose
 (fasting blood sugar of 100 to 125 mg/dL or 5.6 to 7 mmol/L)
 Increased blood pressure
 (130/85 or higher) or if you take medicine for high blood pressure
 Increased fasting levels of triglycerides
 (greater than 150 to 180 mg/dL or 1.7 mmol/L) or decreased fasting HDL
cholesterol (less than 40 mg/dL or 1 mmol/L for men or 50 mg/dL or 1.3
mmol/L for women)
METABOLIC SYNDROME IN
CHILDREN AND ADOLESCENTS
 Definition
Metabolic syndrome also occurs in children and adolescents but
there is no consensus on the definition
 The International Diabetes Federation (IDF) definition of
metabolic syndrome in children 10 to 16 years old is
similar to that used by the IDF for adults, except that the
definition for adolescents uses ethnic-specific waist
circumference percentiles and one cutoff level for HDL rather
than a sex-specific cutoff.
 For children 16 years and older, the adult criteria can be
used.
 For children younger than 10 years of age, metabolic
syndrome cannot be diagnosed, but vigilance is recommended if
the waist circumference is ≥90 percentile.
METABOLIC SYNDROME IN
CHILDREN AND ADOLESCENTS
Risk factors
 Among obese children, the
prevalence of the metabolic
syndrome is high and
increases with worsening
obesity.
 The prevalence of metabolic
syndrome is high among
obese children and
adolescents and increases
with the severity of the
obesity, and with central
adiposity in particular.
Clinical Implications of
Metabolic Syndrome
The definition of metabolic
syndrome may be clinically
useful for risk stratification and
therapeutic intervention in
pediatrics. However, lifestyle
modification that emphasizes
reduction of established risk
factors, such as promotion of
exercise, weight loss, and
smoking cessation, is the main
therapeutic goal in obese
children and adolescents,
regardless of a metabolic
syndrome diagnosis.
METABOLIC SYNDROME
TREATMENT
 Reduce or eliminate underlying problems (eg, obesity, lack of activity) by losing
weight and becoming more active.
 Treat cardiovascular risk factors, such as high blood pressure and cholesterol, if
these problems persist despite losing weight and exercising.
 Weight loss
 The Mediterranean diet is high in fruits, vegetables, nuts, whole grains, and
olive oil
 The DASH (Dietary Approaches to Stop Hypertension) The DASH diet requires
you to eat no more than 2400 mg of sodium per day, four to five servings of
fruit, four to five servings of vegetables, two to three servings of low-fat dairy
products, and all foods must contain less than 25 percent total fat per serving.
 Lifestyle modification — Prevention or reduction of obesity, particularly
abdominal obesity, is the main therapeutic goal in patients with the metabolic
syndrome
 Exercise — . The standard exercise recommendation is a daily minimum of 30
minutes of moderate-intensity (such as brisk walking) physical activity.
Increasing the level of physical activity appears to further enhance the
beneficial effect
METABOLIC SYNDROME and
Polycystic Ovary Syndrome
(PCOS)
 PCOS and Metabolic Sydnrome originally was described by
Stein and Leventhal as the association of amenorrhea with
polycystic ovaries, and variably, hirsutism and obesity
 It is now recognized that PCOS represents a spectrum of
disease characterized primarily by the following features:
 Cutaneous hyperandrogenism (eg, hirsutism, treatment-
resistant acne, and/or pattern balding [androgenetic alopecia]
 Menstrual irregularity (eg, oligo- or amenorrhea, or irregular
bleeding)
 Polycystic ovary
 Obesity and insulin resistance
Clinical Manifestations of The
Insulin Resistance Syndrome in
Children
Polycystic ovary syndrome
(PCOS)
Three sets of diagnostic criteria have been
proposed for the diagnosis of PCOS in adults.
In adolescents, using the NIH diagnostic criteria
in most cases.
 PCOS risk criterion proposed by the Androgen
Excess and PCOS Society (AES), alternatively
defined as hyperandrogenism and a polycystic
ovary, be considered as indicative of risk for
PCOS rather than as diagnostic.
PCOS Prevalence
The prevalence of PCOS in the adolescent population
is unknown.
PCOS DIFFERENTIAL
DIAGNOSIS
 Congenital adrenal
hyperplasia Nonclassic
 Classic CAH due to 21-
hydroxylase deficiency
 Classic CAH, and to a
lesser extent nonclassic
CAH,
 Ovarian steroidogenic
blocks
 Other adrenal disorders
 Cushing's syndrome
include central obesity,
dorsal fat pad,
hypertension, easy
bruising, striae, and
proximal muscle
weakness.
 Hyperprolactinemia
 Acromegaly
 Virilizing tumors
 Thyroid dysfunction
 Drugs
 Disorders of sex
development
 Idiopathic
DIAGNOSTIC CRITERIA
Cutaneous signs of hyperandrogenism (eg,
hirsutism, persistent acne, and/or pattern
alopecia)
Menstrual irregularity (eg, oligo- or amenorrhea,
or irregular bleeding)
 Polycystic ovary syndrome
 Obesity and insulin resistance
DIAGNOSTIC APPROACH.
Evidence of hyperandrogenism — The criterion of
clinical hyperandrogenism is satisfied by
hirsutism or other cutaneous signs of
hyperandrogenism.
Evidence of ovarian dysfunction
Exclusion of non-PCOS causes of
hyperandrogenemia
Additional evaluation after the diagnosis of PCOS
TESTING FOR ANDROGEN
EXCESS
 Total testosterone
 Free testosterone
 Dehydroepiandrosterone sulfate (DHEAS)
 Ultrasonography
 Endocrine Test
 Prolactin
 Thyroid function
 Insulin-like growth factor-I
 Serum cortisol
 Early-morning 17-hydroxyprogesterone
Manifestations of Polycystic Ovary Syndrome in
Approximate Proportion to their Relative
Incidence and Coincidence
ANOVULATORY
SYMPTOMS
OBESITY
HIRSUTISM,ACNE,
ALOPECIA
Pathogenesis
 Intraovarian androgen excess appears to be
responsible for both anovulation and the formation of
multiple ovarian "cysts" because of stimulated
excessive growth of small follicles and hindrance of the
maturation of the dominant follicle.
 There is vigorous debate about whether this pathologic
process is primarily a disorder of pituitary gonadotropin
secretion or a disorder of ovarian and/or adrenal
steroidogenesis.
 PCOS may result from a metabolic disorder that
includes insulin resistance.
 Abnormal pituitary function
 Abnormal steroidogenesis
 Extrinsic factors contributing to dysregulated
steroidogenesis
Abnormal Pituitary Function
 Increased LH relative to FSH was the
first laboratory abnormality identified in
classic PCOS. Elevated LH levels occur
in about half of PCOS patients. Elevated
LH is thought to play a role in the
pathogenesis of PCOS by increasing
androgen production and secretion by
ovarian theca cells.
 Patients with PCOS have an increased
LH pulse frequency and amplitude.
 Obesity seems to attenuate the increase
in LH pulse amplitude, in part because
the pituitary gonadotropes of obese
women with PCOS produce LH isoforms
that are rapidly metabolized.
Abnormal Steroidogenesis
 Alternative hypothesis that PCOS is due to intrinsic
ovarian dysfunction. This hypothesis considers that
primary functional ovarian hyperandrogenism (FOH)
is the essence of PCOS.
 The intraovarian level of androgens in FOH is higher
than in most adrenal causes of androgen excess and
results in excessive growth of small ovarian follicles
while inhibiting follicular maturation and
development of the dominant follicle.
 These result in the polycystic appearance of the
ovary and the anovulatory symptoms.
Extrinsic factors Contributing to
Dysregulated Steroidogenesis
 The insulin/insulin-like growth factors (IGF)
system is capable of acting in synergy with trophic
hormones, contributing to ovarian or adrenal
excess androgen production.
 In the ovary, insulin acts in conjunction with LH to
enhance androgen production and reverse the LH-
induced down-regulation of LH binding sites.
Insulin and IGFs increase the activities of multiple
steroidogenic enzymes in both the ovaries and
adrenal glands.
 This suggests that the hyperandrogenemia and
obesity of PCOS are mechanistically linked.
Treatment for PCOS in
adolescents is directed at
the following clinical
manifestations:
Menstrual irregularity
Cutaneous
hyperandrogenism, primarily
hirsutism and acne
Obesity and insulin resistance
TREATMENT FOR PCOS
Menstrual irregularity should
be treated in adolescents with
PCOS because chronic
anovulation increases the risk
of developing endometrial
hyperplasia, which is
associated with endometrial
carcinoma. In addition,
anemia can result from
dysfunctional uterine bleeding
or menorrhagia.
TREATMENT FOR PCOS
 The combination oral contraceptive pill (OCP), which contains estrogen
and progestin, usually is the first-line treatment for adolescents with
PCOS and menstrual irregularity, especially in patients with cutaneous
signs of androgen excess.
 OCPs induce regular menstrual periods with a higher degree of
reliability than other forms of treatment.
 Progestin inhibits endometrial proliferation, preventing hyperplasia.
Estrogen inhibits the activity of the hypothalamic-pituitary-gonadal
axis, reducing ovarian androgen production as well as increasing serum
sex hormone binding globulin (SHBG) levels.
 OCP therapy also will normalize androgen levels within 18 to 21 days.
 After three months, the efficacy of treatment is assessed by evaluating
clinical symptoms and androgen levels. If the treatment is effective, as
a general rule, OCPs should be continued until the patient is
gynecologically mature (five years postmenarcheal).

TREATMENT FOR PCOS
Limitations — The role of OCPs in the management
of PCOS in adolescents may be limited for several
reasons:
 OCP therapy may make weight loss more difficult to
attain because it promotes salt and water retention.
 The patient may believe the treatment is curative
and defer a definitive diagnostic work-up.
 OCPs do not permit conception if and when it is
desired.
 In perimenarcheal girls with short stature who have
open epiphyses, OCPs are contraindicated because
OCPs contain growth-inhibitory amounts of
estrogen.
TREATMENT FOR PCOS
Progestin
Glucocorticoid
GnRH agonists
OBESITY AND INSULIN
RESISTANCE
 The treatment of obesity
improves ovulation, acanthosis
nigricans, androgen excess,
and cardiovascular risk in
patients with PCOS.
 Weight reduction is indicated in
obese patients with PCOS as
part of a program to reduce
cardiovascular risk factors.
 Diet and exercise are the
first-line treatment for
obese adolescents with
PCOS as for obese individuals
without PCOS.
Insulin Resistance
 Obesity is of major importance in the insulin resistance of PCOS,
although insulin resistance is disproportionate to the degree of
adiposity. Insulin resistance is commonly manifested as
acanthosis nigricans
 The biguanides, of which metformin is the only one available in
the US are thus a potential adjunct in the treatment of PCOS;
thiazolidinediones also are effective in reducing insulin levels,
but have raised safety concerns, as discussed below.
 Although their mechanisms of action differ, both metformin and
thiazolidinediones reduce insulin concentrations, promote
ovulation, and lower androgen levels
 Metformin is the only one of these agents that we currently use
in adolescents with PCOS because of concerns of weight gain
and rare hepatic and possible cardiac toxicity with
thiazolidinediones.
 Randomized, placebo-controlled trials in adolescents and adults
have shown that metformin significantly increases the frequency
of menses and ovulation (by about 50 percent), and lowers
testosterone levels (by about 20 percent).
Pharmacologic Management
Changed Amlodipine 5mg to
Losartan 50mg/tab as
there was no change for
one month.
Prevent target organ damage
and decreased fluid
retention
1st Follow-up April
2012
MY USE COUNSELING/MOTIVATIONAL
INTERVIEW
 I once again asked the patient how she was doing.
How did she feel about the diet change? I asked if
she was fully aware and really understood her
condition.
 “ok lang” “Ginagawa ko rin dahil sa mama ko.”
 I asked her if she still remembers what I told her
about the health risks involved with hypertension
and obesity.
 She said “Opo doc, naala ko naman.”
 I asked her if her overweight condition made her
conscious with her appearance, she said NO during
the 1st consult, but she did admitted that it started
to beome a concern especially when some of her
classmates teases her. She also wanted to be
noticed by her crush.
BEHAVIOR CHANGE TOOL AND
DECISIONAL BALANCE
TECHNIQUE
 I asked her what are her goals in life.
 She said she wants to work as an engineer
and have a family for own. She wants to
travel and meet lots of new friends.
 I asked her what does eating to much and
having a sedentary lifestyle has to do with
her dream...
 “Magkakasakit ako palagi at baka palagi
nasa hospital”.
BEHAVIOR CHANGE TOOL AND
DECISIONAL BALANCE
TECHNIQUE
 I used the Decisional Balance technique for
my patient….
Decisional Balance
 "reflects the individual's relative weighing
of the pros and cons of changing.“
 Decision making was conceptualized by
Janis and Mann as a "decisional balance
sheet" of comparative potential gains and
losses.“
 Decisional balance measures, the pros
and the cons, have become critical
constructs in the Transtheoretical Model
 Sound decision making requires the
consideration of the potential benefits
(pros) and costs (cons) associated with a
behavior's consequences.
Decisional Balance
 Decisional balance is one of the
best predictors of future
change. TTM research has
found the following
relationships between the pros,
cons, and the stage of change
across 48 behaviors and over
100 populations studied.
 The cons of changing outweigh
the pros in the Pre-
contemplation stage.
 The pros surpass the cons in
the middle stages.
 The pros outweigh the cons in
the Action stage
Decisional Balance
Maintaining
Current Use
Changing
Use Pattern
Benefits
Benefits
Costs
Costs
“Masarap”
“Hindi
Magkakasakit”
“Gaganda Ako “
“Mas Okay ang
suot”
“Magkakasakit
ako”
“Mas lalo
tumaba”
“Hindi na
masarap”
BEHAVIOR CHANGE TOOL AND
DECISIONAL BALANCE
TECHNIQUE
She then realized that she
would have to change.
The patient is now willing to
change hence I made a
treatment plan to target
obesity hence decreased
incidence of hypertension.
Hypertension, Metabolic
Syndrome, PCOS
Obesity
Lifestyle modification
Behavioral Change and
Motivation
Treat Obesity Improve symptoms and
minimize health risks
APPROACH ON TREATMENT TO
OBESITY
According the AAP’s Recommendations for
Treatment of Child and Adolescent Overweight and
Obesity—
Comprehensive interventions that include
behavioral therapy along with changes in nutrition
and physical activity are the most closely studied
and seem to be the most successful approaches to
improving long-term weight and health status.
APPROACH ON TREATMENT TO
OBESITY
 In the study…showed a guideline on how to treat
and manage adolescent obesity based on
1. Nutritional Treatment
2. Macronutrient Therapy
3. Food Behaviors
4. Dietary Interventions
5. Physical Activity and Reducing Sedentary
Activities
6. Behavioral Approaches
7. Other Interventions
8. Recommendations of Stages of Treatment
APPROACH ON TREATMENT TO
OBESITY
Nutritional Treatment
In the guideline, it reviewed nutritional treatment for our patient
to decrease obesity which included:
 Fruits and Vegetables
 Fruit Juice
 Sweetened Beverage
 Dairy Food
 Calcium
 Dietary fiber
Eight studies evaluating the relationship between fruit and/or
vegetable intake and body weight were reviewed. All had mixed
results but two studies found an inverse association with
adiposity.
APPROACH ON TREATMENT TO
OBESITY
Macronutrient Therapy
Carbohydrate
Fat
Protein
Glycemic index
 Glycemic index (GI) has been proposed to affect
body weight regulation and risk for obesity-
associated complications.80 The GI is defined as the
area under the glucose dose-response curve after
consumption of 50 g of available carbohydrate from a
test food, divided by the area under the curve after
consumption of 50 g of available carbohydrate from a
control food (either white bread or glucose).
 Short-term feeding studies indicated that hunger and
cumulative food intake were greater 3 to 5 hours
after a high-GI versus low-GI meal, controlled for
macronutrient and energy contents.
FOOD BEHAVIORS
In terms of the FOOD BEHAVIORS of our patient
 Breakfast Skipping
 Snacking
 Eating Out
DIETARY INTERVENTIONS
Balanced-Macronutrient/Low-Energy Diet
Salt reduced-energy diet
The traffic light diet
The Food Guide Pyramid
PHYSICAL ACTIVITY
It used these measurements to calculate physical
activity levels, as follows:
physical activity level-total energy and
expenditure/basal metabolic rate.
Amount of Physical Activity
 The American Academy of Pediatrics recommends
that 30 minutes of this activity occur during the
school day. Very obese children may need to start
with shorter periods of activity and gradually increase
the time spent being active.
 Reducing Sedentary Activities
 Television Viewing and Obesity
Weight Recommendations
According to Age and BMI
Percentile
The AAP guideline provided a systematic approach which to manage
obesity patients. The staged-care process is divided into 4 stages,
that is:
(1) Prevention Plus (healthy lifestyle changes)
(2) Structured weight management
(3) Comprehensive multidisciplinary intervention
(4) tertiary care intervention.
Weight Recommendations According to
Age and BMI
Percentile
NONPHARMACOLOGIC PLAN
 A. Use Prevention Plus Stage 1 Intervention
 Using the algorithm, our patient is at the >99 percentile hence a
Prevention Plus Stage 1 interventions should be based on the
family’s readiness to change and include the following:
1. Consumption of 5 servings of fruits and vegetables per day
2. Minimization or elimination of sugar-sweetened beverages
3. Limits of 2 hours of screen time per day, no television in the
room where the child sleeps, and no television viewing
4. 1 hour of physical activity per day
 Physical activity can be increased gradually for sedentary
children. Children may be unable to achieve 1 hour of activity
per day initially but can gradually increase activity to reach 1
hour/day.
B. Stricter implementation on the Diet
Low Energy Diet of 2000kcal C350 P75 F 35
from a 3022kcal diet and a strict decrease of
salt content.
C. Establishing an exercise plan
Jogging at their area for 40 min starting from
moderate to vigorous aerobic-based physical
activity 3–5 days/week.
NONPHARMACOLOGIC PLAN
My plan for Metabolic Syndrome
My Plan for PCOS
2nd follow-up May 2012
 S> Weight loss of 8 pounds for 2 monthS.
Lessen of BP from 150/90 to 130/80…
No OB consult yet.Patient was advised to take OB
consult in the near future.Patient still has no
menstruation.
Management
 Maintain medicines and continued diet and
exercise plan.
 Stop Losartan
I also advised that their family; the parents and
her brothers and sisters to seek consult for the
obesity problem as well.
3rd Follow-up August 2012
 Patient had weight loss of 2 pounds but having
trouble to maintain diet and exercise during
the school year due to the availability of food
and temptations. BP lowered to 120/80.
Patient started to play badminton with family
and still continue to jog if she has free time.
Plan:
 Advise to have a more structured diet and
exercise to adapt to school by having a list of
food to eart in day. Patient was advised to
have cooked food from home
September 2012
S>
Plan
Long Term Plan
PSYCHOSOCIAL ISSUES -
ADOLESCENT ISSUES
Self-Image
Addiction to TV and
Facebook
Role of parents in
adolescence
WELLNESS PLAN FOR THE
PATIENT
Lifestyle
 Continue the Prevention Plus Plan for our patient
with a advice increase Physical and outdoor
activities.
Screening
 Patient was advised an annual screening to detect
organ damage and risk of other disease like Type
II Diabetes
 Immunizations- Influenza vaccine yearly, Varicella
vaccine.
GOING BACK TO THE PATIENT
 The good news is that the
patient’s BP is at 120-130/80-90.
 Patient hasn’t made substantial
weight loss, but the good thing is
that during the past three
months her lifestyle changed
dramatically when compared
alongside the years that she was
excessively eating. She started
to gain self-confidence since the
change of eating habits. The
family changed their eating
habits and have modified their
lifestyle accordingly too.
Insight
Holistic care
Interrelationship of Diseases
The Importance of Lifestyle for being Healthy
Counseling and Motivation Behavior change as
part of being a Doctor
The power of change
Caring for patient is not a shot deal, have to do
lots of follow-up and evaluation
Importance of education and value formation in
children and adults ( School and Government)
Insight
Suggestions:
 Comprehensive Government Plan to Educate and
Change the Lifestyle of our Youth
 Insight (slide)
My message to everyone…
 As doctors, we are privileged to have the power
to change lives. Let us go forth and use this
opportunity to be an instrument towards positive
change.

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The power of change

  • 1. A Clinical Case Presentation The Power of Change: A Case of a Adolescent with Multiple Medical Condition Alejandro E. Legarda III MD First Year Resident DFCM
  • 2. Objectives • To present an adolescent with hypertension and obesity and its correlation to Metabolic syndrome and PCOS • To discuss the differential diagnosis for high BP in the young • To discuss the approach to management of adolescent with hypertension, obesity and the diagnose syndromes • To present short-term and long-term wellness plan appropriate for the patient's condition
  • 3. Patient Profile EJ 13 years old Single Roman Catholic Incoming 3rd year high school student Chief Complaint ELEVATED BLOOD PRESSURE
  • 4. Clinical History Five years prior to consult (2007) • The patient was then eight years old and sought a consult due to her re- occurring erythematous vesicular lesions. • Upon consultation, she was diagnosed with Post-streptococcal glomerulonephritis. The patients was admitted in the hospital for a week due to this condition. • Patient was documented to suffer from hypertension. Nifedipine was prescribed to control and manage her hypertension. After hospitalization, patient felt well again. No follow-up consult was recommended to the patient.
  • 5. Three years prior to consult (2009) • The patient started gaining weight as food intake severely increased. • Patient’s BP was taken annually in school and showed elevated blood pressure. • The increased blood pressure readings was simply ignored by the patient and her parents, thus resulting in progressive, uncontrolled weight gain. Clinical History
  • 6. Two weeks prior to consult • Patient sought consultation at the UP-PGH Dermatological Department for her vesicular lesions. • Patient featured an incidental finding of 160-90 blood pressure reading. • Assessment reveals: Acne vulgaris with etiology related to PCOS Hypertension secondary to (1) PCOS (2) Cushing’s Syndrome (3) Insect bite hyper sensitivity reaction Patient was given: • Amlodipine (5mg./tab) OD • Benzoyl Peroxide gel OD • Tretinoin cream for the face • Cloxacilin (500mg./tab) for 7 days • Mupirocin Bethamethasone ointment ITD • Sunscreen • mild soap Clinical History Patient was referred to Pedia adolescent, hence the consult.
  • 7. Clinical History  At Consult (March 26, 2012)  Patient was seen at the Pedia Adolescent Clinic
  • 8. Review of Systems (+) polyuria (+) polydipsia (-) rashes (-) epistaxis (-) gum bleeding (-) neck pain (-) dysphagia (-) chest pain (-) orthopnea (-) dyspnea on exertion (-) orthopnea (-) edema (-) neck pain (-) abdominal pain (-) constipation (-) diarrhea (-) urgency (-) frequency (-) dysuria (-) nocturia (-) hematuria (-) heat intolerance (-) jaundice
  • 9. Past Medical History (-) Asthma (-) Allergy (-) Pulmonary Tuberculosis (-) Bronchial asthma No Accident and injury Hospitalizations: Admitted for (+) PSGN (2007) and Dengue Fever (2009) Surgeries: There was no previous surgery Medications: Co-amoxiclav for her recurrent skin infections
  • 10. OB/GYNE History Menarche: January 2011 Irregular flow occurring only 3x since her menarche Lasting 4-5 days, Pads 2-4 a day No dysmenorrhea No sexual contact
  • 11. Birth and Maternal History Patient was born full-term via spontaneous vaginal delivery at a local hospital delivered by an obstetrician with no known feto-maternal complications.
  • 12. NUTRITIONAL HISTORY Patient was breastfed for 3 months and then shifted to bottle feeding of Bona milk every 3 to 4 hours starting at 4 months old up to 12 months old. Complementary feeding was started at 6 months old. Patient would skip breakfast but would have 2 snacks before a heavy lunch. She would have 2 heavy meriendas, e.g.,2 hamburgers/hotdogs or cups of ice cream .Most of the food she eats are either fried or salty and plenty of desserts. She loves to drink cola.
  • 13. Immunization History Childhood Vaccinations Bacillus Calmette-Guerin (BCG), one dose Hepatitis B vaccine, three doses Diptheria Pertussis Tetatnus (DPT), three doses Oral Polio Vaccine, thress doses Measles, one dose
  • 14. FAMILY GENOGRAM I II III Jorgo Family March 26, 2012 Hypertension Accident Overweight Diabetes 76 80 68 75 56 54 32 50 46 52 48 19 18 15 13 Elaisa JJMJ EJ
  • 15. Personal and Social History Home: - lives with parents and four siblings in Imus, Cavite -good relationship with parents and siblings Education: -Incoming third-year high school student -With above-average grades - has close set of friends in school Activities: -Favorite past time– eating -Loves eating street foods and junk foods -Spends most of her free time in front of the TV or computer -Not involved in any outdoor activities such as sports
  • 16. Personal and Social History Drugs: -No history of cigarette or alcohol use -Denies use or history of use of illicit drugs Sexual: -Does not showcase any consciousness with body weight and shape -Patient has not attempted to change her appearance -Currently no relationship with the opposite sex Suicidal Tendencies: -Patient exhibits no signs or episodes of depression or suicidal ideation Safety: -Patient together with her family lives in a peaceful and orderly community with minimum crime rate - uses public transportation to commute -Not a member of a gang or sorority
  • 17. Physical Examination General Survey: Awake, alert, coherent, in pain, not in cardio-respiratory distress (-) muscle wasting (-) moon face (-) proximal muscle weakness (-) buffalo hump Vital Signs: Blood Pressure: 150/90(>99th percentile) Heart Rate: 75 beats/minute Respiratory Rate: 18 breaths/minute Temperature: 36.8 C
  • 18. Physical Examination Anthropometrics: Height: 157 cm Weight: 96.5 kg Body Mass Index: 40.7 kg/m2 (Z score: 2.58) Abdominal Circumference 102cm
  • 19. Physical Examination Head and Neck: Anicteric sclerae, pink conjunctivae, pupils 2-3mm OU reactive to light, (+) Short leg length (+) Acanthosis nigricans, (-) masses, (-) cervical lymphadenopathy, (-) anterior neck mass (-) tonsillopharyngealcongestion, (-) neck vein engorgement, (-)ear discharge
  • 20. Physical Examination Chest and Lungs: Equal chest expansion, no deformities, no lesions, clear breath sounds, (-) crackles/rales/wheezes Heart: Adynamic precordium, distinct heart sounds, apex beat at 5th intercostal space left midclavicular line, regular rate and rhythm, no murmurs
  • 21. Physical Examination Abdomen: flabby (+) Striae lower abodomen no deformities no lesions Soft normoactive bowel sounds (-)masses or tenderness liver span 8 cm right midclavicular line intact Traube’s space no costo-vertebral angle tenderness
  • 22. Physical Examination Extremities pink nailbeds full and equal pulses no cyanosis/clubbing/ edema no crepitations no limitation of passive and active motion on both upper extremities (-) shooting pain on straight leg raise of both lower extremities (-) limitation of motion due to pain no crepitations on hips, knees or ankles no joint swelling or deformities (-) Pain on active leg raise of both lower extremities
  • 23. Physical Examination Neuro Exam Cranial Nerve (CN) Examination CN I –intact gross olfaction CN II –pupils 2-3 mm OU briskly reactive to light CN III,IV,VI –full range of extraocular muscle movement CN V –brisk corneals, good masseter tone, CN VII –no facial asymmetry, no altered taste CN VIII –intact gross hearing, no lateralization on Weber Test CN IX –no altered taste, can swallow CN X –can swallow CN XI –good symmetrical shrug CN XII –can protrude tongue, no deviation
  • 24. Physical Examination Sensory Pain: Intact on all dermatomes Light Touch: Intact on all dermatomes Vibratory: Intact on all dermatomes Motor Normal Gait Good muscle tone, no atrophy, no limb size discrepancy Full motor strength on both upper extremities Tanner Stage 3 External genitalia with dark, coarse curly hair spreads over mons pubis Elevation of Breast contour; areolae enlarged
  • 25. Salient Features of the Case SALIENT FEATURES OF THE CASE A 13-year old female Chief complaint of elevated blood pressure History of hypertension ,DM and Obesity Previous history of renal disease (+) poluyuria, (+) polyphaga. Amenorrhea Obesity Anthropometrics: Height: 157 cm, Weight: 96.5 kg, Body Mass Index: 40.7 kg/m2 (Z score: 2.58), (+) Short neck length (+) Acanthosis nigricans nape area, Flabby abdomen with (+) Striae
  • 26. Initial Impression Hypertension, Stage II-- etiology to be determined Acne Vulgaris probably secondary to PCOS DM suspect Obese, Type 2 Amenorrhea secondary to PCOS
  • 27. Management Diagnostics: Complete Blood Count (CBC) Plasma sodium, potassium and calcium BUN, Creatinine Fasting plasma glucose Lipid profile Urinalysis Whole AB ultrasound Chest X--ray ECG TSH, FT4
  • 28. Therapeutics Continue the following medications: Cloxacillin 500 for 7 days Tretnoin Cream for the face Mupirocine Betamethasone ointment, TID Sun screen use Mild soap use Start Amlodipine 5mg once a day
  • 30. European Society of Hypertension The study mentioned childhood BP has been shown to track into adulthood Unlike adults, the diagnostic criteria for elevated BP in children are based on the concept that BP in children increases with age and body size, making it impossible to utilize a single BP level to define hypertension.
  • 31. The recommended method is auscultatory. Use K1 for systolic BP and K5 for diastolic B. If the oscillometric method is used, the monitor needs to be validated and if hypertension is detected by the oscillometric method, it needs to be confirmed using the auscultatory method. The Use the appropriate cuff size according to arm width (40% of the arm circumference) and length (4_8 cm, 6_12 cm, 9_18 cm, 10_24 cm, to cover 80–100% of the individual’s arm circumference). Specific recommendations for office BP measurement in children and adolescents
  • 32. Blood Pressure for Girls by Age and Height Percentiles
  • 33.
  • 34. Systolic and diastolic ambulatory blood pressure (systolic/diastolic) values for clinical use
  • 35. Task Force for Blood Pressure in Children, the Fourth Report on the Diagnosis, Evaluation, and Treatment of High Blood Pressure in Children and Adolescents The normal BP in children is defined as SBP and DBP less than 90th percentile for age, sex and height. Hypertension is defined as SBP and/or DBP persistently 95th percentile or more, measured on at least three separate occasions with the auscultatory method. Rule out White-coat (or isolated office) and masked (or isolated ambulatory) hypertensions
  • 36. Definition and Classification of Hypertension in Children and Adolescents
  • 37. Diagnostic Algorithm of Hypertension
  • 38. FAMILY HISTORY Hypertension Cardiovascular and cerebrovascular disease Diabetes mellitus Dyslipidemia Obesity Hereditary renal disease (Policystic kidney disease) Hereditary endocrine disease (pheochromocytoma glucocorticoid-remediable aldosteronism, multiple endocrine neoplasia type 2, von Hippel–Lindau) Syndromes associated with hypertension (neurofibromatosis) Clinical Data To Note
  • 39. Clinical Data To Note PERINATAL HISTORY Birth weight, gestational age, oligohydramnios, anoxia, umbilical artery catheterization PREVIOUS HISTORY Hypertension Urinary tract infection, renal or urological disease Cardiac, endocrine (including diabetes) or neurological disease Growth retardation Symptoms suggestive of secondary hypertension Dysuria, thirst/polyuria, nocturia, hematuria Edema, weight loss, failure to thrive Palpitations, sweating, fever, pallor, flushing Cold extremities, intermittent claudication Virilization, primary amenorrhea and male pseudohermaphroditism Symptoms suggestive of target organ damage Headache, epistaxis, vertigo, visual impairment Facial palsy, fits, strokes Dyspnea
  • 40. Clinical Data To Note Sleep history: Snoring apnea, daytime somnolence Risk factor history: Physical exercise, dietary habits Smoking, alcohol Drug intake: Anti-hypertensives Steroids, cyclosporine tacrolimus or otherTri-cyclic anti-depressants atypical antipsychotics decongestants Oral contraceptives illegal drugs Pregnancy
  • 41. Physical Examination To Note Height Weight Body mass index External features of syndromes/conditions associated with hypertension Neurofibromatosis Klippel–Trenaunay–Weber Feuerstein–Mims Von Hippel–Lindau Multiple endocrine neoplasia Pseudoxanthoma elasticum Turner, William Marfan Cushing Hyperthyroidism, Lupus Vasculitis Congenital adrenal hyperplasia Data to record:
  • 42. Physical Examination Data to Record Cardiovascular examination Pulse and BP measurement in both arms and legs Bruits/murmurs – heart, abdomen, flanks, back, neck, head Signs of left ventricular hypertrophy or cardiac failure Abdomen Masses – Wilms, neuroblastoma, pheochromocytoma, autosomal dominant and recessive polycystic kidney disease, multicystic kidney displasia, obstructive uropathy Hepatosplenomegaly – autosomal recessive polycystic kidney disease Neurological examination Fundoscopy for hypertensive changes and retinal amartoma (von Hippel–Lindau) Evidence of VIII nerve palsy Other neurological defects including stroke
  • 43. Indicators on Physical Exam of Etiology of Hypertension in a Child Thyromegaly Hyperthyroidism Acne, hirsutism, striae Cushing syndrome, anabolic steroid abuse Cafe´-au-lait spots Neurofibromatosis Adenoma sebaceum Tuberous sclerosis Malar rash Systemic lupus erythematosus Acanthrosis nigricans Type 2 diabetes Chest widely spaced nipples Turner syndrome Heart murmur Coarctation of the aorta Friction rub Systemic lupus erythematosus (pericarditis), Abdomen Mass Wilms tumor, neuroblastoma, pheochromocytoma Epigastric/flank bruit Renal artery stenosis Palpable kidneys Polycystic kidney disease, hydronephrosis, multicysticdysplastic kidney Genitalia Ambiguous/virilization Adrenal hyperplasia Extremities Joint swelling Systemic lupus erythematosus, collagen vascular ds Muscle weakness Hyperaldosteronism, Liddle syndrome
  • 44. Patient PE Presentation Significant Anthropometrics: Height: 157 cm Weight: 96.5 kg, Body Mass Index: 40.7 kg/m2 (Z score: 2.58) (+) Short neck length (+) Acanthosis nigricans nape area Flabby abdomen with (+) Striae (+) Acne Other details were none pertinent
  • 45. Target Organ Damage To Note Heart Blood Vessels Kidney Neuro Fundoscopy
  • 46. Heart Left Ventricular Hyperthrophy (LVH) remains to date the most thoroughly documented form of end-organ damage caused by hypertension in children and adolescents.
  • 47. Blood Vessels Morphological changes of the arterial wall, thickening of the intima-media complex. Children with familial hypercholesterolemia have higher IMT Overweight and obesity are associated with increased IMT in children with or without essential hypertension.
  • 48. Kidney Hypertension-related renal damage is based on a reduced renal function or an elevated UAE. Proteinuria is a marker of glomerular damage in primary and secondary glomerulopathies. An indication for BP- lowering interventions. Microalbuminuria (20–300mg/g creatinine, 2–30 mg/mmol creatinine, 30–300 mg/day, 20–200mg/min) has been shown to predict the development of diabetic nephropathy . Overt proteinuria (>300 mg/day) indicates the existence of established renal parenchymal damage.
  • 49. Neuro and Fundoscopy Cerebral seizures, stroke, visual impairment and retinal vascular changes are complications associated with severe hypertension. Fundoscopy was also done in because in a study of 97 children and adolescents with essential hypertension, found that 51% displayed retinal abnormalities, as detected from direct ophthalmoscopy.
  • 50. Obesity and Hypertension Using the 2000 CDC growth charts, at risk of overweight for ages 2 to 20 years overweight is defined as a Body Mass Index (BMI)-for-age between the 85th and the 95th percentiles. Overweight in children is defined as a BMI-for-age at or above the 95th percentile on the charts. BMI is weight in kilograms divided by height in meters squared (kg/m2). BMI is used differently to define overweight in children and adolescents than it is in adults. In children and adolescents, BMI changes with age and gender.
  • 51. Obesity and Hypertension Overweight children and adolescents are at increased risk for various chronic diseases in later life. The psychosocial consequences of overweight are significant. Overweight in children has been linked to social discrimination, a negative self-image in adolescence that often persists into adulthood, parental neglect, and behavioral and learning problems.
  • 52. Obesity and Hypertension Being overweight is probably the most important of the conditions associated with elevated BP in childhood and accounts for more than half the risk for developing hypertension. Adiposity is the most powerful risk factor for higher BP. Waist circumference (abdominal obesity) has been shown to play a role. Dietary habits like high salt intake, have been implicated as factors favoring higher BP values.
  • 53. Obesity and Hypertension The CDC mentions the Common Medical Consequences of Overweight (Dietz, 1998) hyperlipidemia glucose intolerance hepatic steatosis cholelithiasis sleep apnea Obesity hypoventilation syndrome hypertension a variety of orthopedic complications
  • 54. Laboratory Investigations Full blood count Plasma sodium, potassium and calcium, urea, creatinine Fasting plasma glucose Serum lipids (cholesterol, LDL cholesterol, HDL cholesterol) Fasting serum triglycerides Urinalysis plus quantitative measurement of microalbuminuria and proteinuria Renal ultrasound Chest Xray, ECG and 2-D echocardiography Routine tests that have to be performed in all hypertensive children
  • 55.  Recommended additional screening tests  Plasma renin activity, plasma aldosterone concentration  Urine and plasma catecholamines or metanephrines  Tc99 dimercaptosuccı´nic acid scan  Urinary free cortisol  More sophisticated tests that should await results of  above screening  Color Doppler ultrasonography  Captopril primed isotope studies  Renal vein renin measurements  Renal angiography  I123 metaiodobenzylguanidine scanning  Computed tomography/ Magnetic resonance imaging  Urine steroid analyses and more complex endocrine  investigations  Molecular genetic studies (Apparent mineralocorticoid  excess, Liddle’s syndrome, etc)
  • 56. SECONDARY HYPERTENSION Sustained hypertension can be classified as secondary when a specific cause can be found, then it can be corrected with specific intervention. There should be work-up should be done if hypertension .
  • 57. Diagnosis of Secondary Causes of Hypertension
  • 58.
  • 59. MY MANAGEMENT Diagnostic Examinations Laboratory Plan: Complete blood count Plasma sodium, potassium and calcium, BUN, Crea Fasting plasma glucose Lipid Profile Urinalysis Whole AB ultrasound Chest Xray, ECG TSH, FT4
  • 60. APPROACH TO MANAGEMENT Non pharmacologic Strategy Recommendations: GOALS: BMI<85th percentile: Maintain BMI to prevent becoming overweight BMI 85–95th percentile: Weight maintenance (younger children) or gradual weight loss in adolescents To reduce BMI to <85th percentile BMI>95th percentile: Gradual weight loss (1–2 kg/ month) to achieve value <85th percentile
  • 61. GENERAL RECOMMENDATIONS Moderate to vigorous physical aerobic activity--40 min, 3–5 days/week and avoid more than 2 hours daily of sedentary activities Avoid intake of excess sugar, excess soft drinks, saturated fat and salt and recommend fruits, vegetables and grain products Implement the behavioural changes (physical activity and diet) tailored to individual and family characteristics Involve the parents/family as partners in the behavioural change process Provide educational support and materials Establish realistic goals Develop a health-promoting reward system Competitive sports participation should be limited only in the presence of uncontrolled stage 2 hypertension
  • 62. For my patient… A. Counseling and Implement Behavioural Change 1.CEA(Catharsis Education Action): Patient 2.Motivational Interviewing- Pre Contemplation stage 3. CEA(Catharsis Education Action): : Parents
  • 63. Counseling and Implement Behavior Change: CEA Patient Patient was not so much concerned of her weight. She doesn’t know the risk and the health issues regarding hypertension. She was not aware why she came to PGH for consult and really wanted to go home. She was also not aware her that being overweight has some health risks as well.
  • 64. Use of Motivational Intervierwing Transtheoretical Model, "process involving progress through a series of stages:"  Precontemplation (Not Ready)-"People are not intending to take action in the foreseeable future, and can be unaware that their behaviour is problematic.”  Contemplation (Getting Ready)-"People are beginning to recognize that their behaviour is problematic, and start to look at the pros and cons of their continued actions.“  Preparation (Ready)-"People are intending to take action in the immediate future, and may begin taking small steps toward behaviour change.“  Action – "People have made specific overt modifications in modifying their problem behaviour or in acquiring new healthy behaviours.“  Maintenance – "People have been able to sustain action for awhile and are working to prevent relapse."
  • 65.
  • 66. Use of Motivational Intervierwing Motivational Interviewing- Pre Contemplation stage Patient was on pre -contemplation stage at that time and I was hoping to make her aware and give her insight to bring her to the stage where she can contemplate. When I asked about her hypertension, she said she knew had it for years but no one told her about the dangers.
  • 67. B. Counseling and Implement Behavior Change 3. CEA: Parents The parents are also unaware of the risk of hypertension and the eating habits and lifestyle that increase her obesity. They couldn’t believe that this would happen at her age. The whole family is at risk since everyone except the wife is obese.
  • 68. My Management Plan for the Patient… Non-pharmacologic strategies A. Counseling and Behavior Change- Done B. I advised the patient to have Regular BP monitoring at home C. Physical Activity: I mentioned to the patient to start to lessen sedentary activities and start to walk more around the subdivision and play with pets. A Exercise program was not done yet as I want for the patient to reach the preparation/action D. Eating Habits: Change of eating was advised. The Patient love to skip breakfast and lessen snack intake. E. A Diet Program: I was planning to put the patient into a low Energy Diet of 2000kcal C350 P75 F 35 from a 3022kcal diet on the next follow up
  • 69. Approach to Medical Management on Hypertension Pharmacologic/Therapeutic Strategies Aside from the non-pharamacologic strategies, I had a dilemma on how will I use therapeutic strategies for my patient EVIDENCE FOR THERAPEUTIC MANAGEMENT Reduce mortality and sequelea in life-threateningconditions Reduce left ventricular hypertrophy Reduce urinary albumin excretion Reduce rate of progression to end-stage renal disease
  • 70. Approach to Medical Management on Hypertension Therapeutic management of hypertension Indications for Antihypertensive Drug Therapy in Children Symptomatic Hypertension Secondary hypertension Hypertensive target-organ damage Diabetes (types 1 and 2) Persistent hypertension despite non-pharmacologic measures >99 percentile BMI
  • 71.
  • 72. Approach to Medical Management on Hypertension Therapeutic Management Treating Hypertension with drugs are most indicated in end organ damage of the Heart and Kidney/Renal Effect to Organ Damage: In the Heart, Regression of LVH was reported in three children with essential hypertension receiving enalapril, in 19 children with primary and secondary hypertension treated with ramipril for 6 months, and in 65 children with chronic kidney disease (CKD) stage 2–4 receiving ramipril for up to 2 years. In Renal: the Effect of Strict Blood Pressure Control and ACE Inhibition on Progression of Chronic Renal Failure in Pediatric Patients (ESCAPE) trial, which has shown efficient BP and proteinuria reduction for the ACE inhibitor ramipril in 352 children with CKD
  • 73. Approach to Medical Management on Hypertension Monotherapy Choice of anti-hypertensive agents ACEIs Angiotensin receptor antagonists (ARBs) Calcium antagonists Beta-blockers Diuretics Combination therapy In children with renal disease, monotherapy is often not sufficient to achieve adequate BP control. Therefore, early combination therapy is required. The best choices of antihypertensive drug combinations are those recommended in the ESH/ESC 2007 Guidelines .
  • 74. Clinical conditions for which specific antihypertensive drug classes are recommended or contraindicated
  • 75. My Therapeutic Management For our patient, she was given a monotherapy of Amlopidine, 5mg./tab once daily.
  • 76. Initial Management summary  Diagnostic Examinations  Laboratory Plan:  Complete blood count  Plasma sodium, potassium and calcium,  BUN, Crea  Fasting plasma glucose  Lipid Profile  Urinalysis  Whole AB ultrasound  Chest Xray, ECG  TSH, FT4
  • 77. Initial Management summary  Non-pharmacologic strategies  Counseling and Behavior Change- Done  B. I advised the patient to have Regular BP monitoring at home  C. Physical Activity: I mentioned to the patient to start to lessen sedentary activities and start to walk more around the subdivision and play with pets. A Exercise program was not done yet as I want for the patient to reach the preparation/action  D. Eating Habits: Change of eating was advised. The Patient love to skip breakfast and lessen snack intake.  E. A Diet Program: I was planning to put the patient into a low Energy Diet of 2000kcal C350 P75 F 35 from a 3022kcal diet on the next follow up
  • 78. Initial Management summary Medical Theraphy  For our patient, she was given a monotherapy of Amlopidine, 5mg./tab once daily.
  • 79. 1st Follow-up April 2012 Maintained BP 150/90…no decrease in BP despite of Amlodipine 5mg tablet. Started to jog for several minutes around the house and roam around the area with her dog. Lessened her calorie intake thanks to the parents modifying the food menu at home. Parents started to prepare healthier food with less salt content. Parents have been very supportive. Siblings stopped eating with the patient for snacks and joined the patient in jogging as well. One of her sibling, who still was a bad influence to her was transferred to their grandmother’s house.
  • 80. 1st Follow-up April 2012  1st Follow-up April 2012 Results  Hgb:139, Hct 0.432, Plt 356 WBC 8.7  Urinalysis : Dark yellow, 1.030, RBC 0-2, WBC 3-4 EC 3+ Sugar (-) Albumin (-)  CXR: Normal Chest Findings  Thyriod FT4- 20.6, Free T3- 5.5, TSH IRM 6.1  Glucose 6.4, BUN 3.30, Crea 45.5, Chole 5.0, Trigly 5.01 HDL 0.98, LDL 1.74, AST 38, ALT 46, Albumin 42 Calcium 2.44, Na- 138, K 4.8  ECG- Sinus Rhythm, Within Normal Limits  Whole Ab Ultrasound: normal  With the current labs results, I was able to rule out many etiology of hypertension including the secondary ones however there was elevation in Triglyceride and there was Impaired Fasting Glucose
  • 81. 1st Follow-up April 2012  Previous Salient Features… SALIENT FEATURES OF THE CASE 13-year old female Chief complaint of elevated blood pressure History of hypertension ,DM and Obesity Previous history of renal disease (+) poluyuria, (+) polyphaga. Amenorrhea Obesity (+) Short neck length (+) Acanthosis nigricans nape area, (+) Striae New Finding from the Diagnostics Impaired Fasting Glucose Elevated Triglyceride Ruled out Cardiovascular, Renal and some secondary etiology
  • 82. 1st Follow-up April 2012  Hypertension stage II secondary to 1) Obesity 2) Metabolic Syndrome  T/c PCOS sedondary to Metabolic Syndrome  Hyperlipidemia  Impaired Fasting Glucose
  • 83. METABOLIC SYNDROME  Group of characteristics:  Most expert groups define metabolic syndrome as the presence of three or more of the following characteristics in a person:  Obesity, especially in the abdominal area  (defined by some groups as a waist size greater than 94 to 102 cm (38 to 41 in) in men or greater than 80 cm (32 in) in women)  Impaired fasting glucose  (fasting blood sugar of 100 to 125 mg/dL or 5.6 to 7 mmol/L)  Increased blood pressure  (130/85 or higher) or if you take medicine for high blood pressure  Increased fasting levels of triglycerides  (greater than 150 to 180 mg/dL or 1.7 mmol/L) or decreased fasting HDL cholesterol (less than 40 mg/dL or 1 mmol/L for men or 50 mg/dL or 1.3 mmol/L for women)
  • 84. METABOLIC SYNDROME IN CHILDREN AND ADOLESCENTS  Definition Metabolic syndrome also occurs in children and adolescents but there is no consensus on the definition  The International Diabetes Federation (IDF) definition of metabolic syndrome in children 10 to 16 years old is similar to that used by the IDF for adults, except that the definition for adolescents uses ethnic-specific waist circumference percentiles and one cutoff level for HDL rather than a sex-specific cutoff.  For children 16 years and older, the adult criteria can be used.  For children younger than 10 years of age, metabolic syndrome cannot be diagnosed, but vigilance is recommended if the waist circumference is ≥90 percentile.
  • 85. METABOLIC SYNDROME IN CHILDREN AND ADOLESCENTS Risk factors  Among obese children, the prevalence of the metabolic syndrome is high and increases with worsening obesity.  The prevalence of metabolic syndrome is high among obese children and adolescents and increases with the severity of the obesity, and with central adiposity in particular.
  • 86. Clinical Implications of Metabolic Syndrome The definition of metabolic syndrome may be clinically useful for risk stratification and therapeutic intervention in pediatrics. However, lifestyle modification that emphasizes reduction of established risk factors, such as promotion of exercise, weight loss, and smoking cessation, is the main therapeutic goal in obese children and adolescents, regardless of a metabolic syndrome diagnosis.
  • 87.
  • 88. METABOLIC SYNDROME TREATMENT  Reduce or eliminate underlying problems (eg, obesity, lack of activity) by losing weight and becoming more active.  Treat cardiovascular risk factors, such as high blood pressure and cholesterol, if these problems persist despite losing weight and exercising.  Weight loss  The Mediterranean diet is high in fruits, vegetables, nuts, whole grains, and olive oil  The DASH (Dietary Approaches to Stop Hypertension) The DASH diet requires you to eat no more than 2400 mg of sodium per day, four to five servings of fruit, four to five servings of vegetables, two to three servings of low-fat dairy products, and all foods must contain less than 25 percent total fat per serving.  Lifestyle modification — Prevention or reduction of obesity, particularly abdominal obesity, is the main therapeutic goal in patients with the metabolic syndrome  Exercise — . The standard exercise recommendation is a daily minimum of 30 minutes of moderate-intensity (such as brisk walking) physical activity. Increasing the level of physical activity appears to further enhance the beneficial effect
  • 89.
  • 90. METABOLIC SYNDROME and Polycystic Ovary Syndrome (PCOS)  PCOS and Metabolic Sydnrome originally was described by Stein and Leventhal as the association of amenorrhea with polycystic ovaries, and variably, hirsutism and obesity  It is now recognized that PCOS represents a spectrum of disease characterized primarily by the following features:  Cutaneous hyperandrogenism (eg, hirsutism, treatment- resistant acne, and/or pattern balding [androgenetic alopecia]  Menstrual irregularity (eg, oligo- or amenorrhea, or irregular bleeding)  Polycystic ovary  Obesity and insulin resistance
  • 91.
  • 92. Clinical Manifestations of The Insulin Resistance Syndrome in Children
  • 93. Polycystic ovary syndrome (PCOS) Three sets of diagnostic criteria have been proposed for the diagnosis of PCOS in adults. In adolescents, using the NIH diagnostic criteria in most cases.  PCOS risk criterion proposed by the Androgen Excess and PCOS Society (AES), alternatively defined as hyperandrogenism and a polycystic ovary, be considered as indicative of risk for PCOS rather than as diagnostic.
  • 94.
  • 95.
  • 96. PCOS Prevalence The prevalence of PCOS in the adolescent population is unknown.
  • 97. PCOS DIFFERENTIAL DIAGNOSIS  Congenital adrenal hyperplasia Nonclassic  Classic CAH due to 21- hydroxylase deficiency  Classic CAH, and to a lesser extent nonclassic CAH,  Ovarian steroidogenic blocks  Other adrenal disorders  Cushing's syndrome include central obesity, dorsal fat pad, hypertension, easy bruising, striae, and proximal muscle weakness.  Hyperprolactinemia  Acromegaly  Virilizing tumors  Thyroid dysfunction  Drugs  Disorders of sex development  Idiopathic
  • 98. DIAGNOSTIC CRITERIA Cutaneous signs of hyperandrogenism (eg, hirsutism, persistent acne, and/or pattern alopecia) Menstrual irregularity (eg, oligo- or amenorrhea, or irregular bleeding)  Polycystic ovary syndrome  Obesity and insulin resistance
  • 99. DIAGNOSTIC APPROACH. Evidence of hyperandrogenism — The criterion of clinical hyperandrogenism is satisfied by hirsutism or other cutaneous signs of hyperandrogenism. Evidence of ovarian dysfunction Exclusion of non-PCOS causes of hyperandrogenemia Additional evaluation after the diagnosis of PCOS
  • 100. TESTING FOR ANDROGEN EXCESS  Total testosterone  Free testosterone  Dehydroepiandrosterone sulfate (DHEAS)  Ultrasonography  Endocrine Test  Prolactin  Thyroid function  Insulin-like growth factor-I  Serum cortisol  Early-morning 17-hydroxyprogesterone
  • 101. Manifestations of Polycystic Ovary Syndrome in Approximate Proportion to their Relative Incidence and Coincidence ANOVULATORY SYMPTOMS OBESITY HIRSUTISM,ACNE, ALOPECIA
  • 102. Pathogenesis  Intraovarian androgen excess appears to be responsible for both anovulation and the formation of multiple ovarian "cysts" because of stimulated excessive growth of small follicles and hindrance of the maturation of the dominant follicle.  There is vigorous debate about whether this pathologic process is primarily a disorder of pituitary gonadotropin secretion or a disorder of ovarian and/or adrenal steroidogenesis.  PCOS may result from a metabolic disorder that includes insulin resistance.  Abnormal pituitary function  Abnormal steroidogenesis  Extrinsic factors contributing to dysregulated steroidogenesis
  • 103. Abnormal Pituitary Function  Increased LH relative to FSH was the first laboratory abnormality identified in classic PCOS. Elevated LH levels occur in about half of PCOS patients. Elevated LH is thought to play a role in the pathogenesis of PCOS by increasing androgen production and secretion by ovarian theca cells.  Patients with PCOS have an increased LH pulse frequency and amplitude.  Obesity seems to attenuate the increase in LH pulse amplitude, in part because the pituitary gonadotropes of obese women with PCOS produce LH isoforms that are rapidly metabolized.
  • 104. Abnormal Steroidogenesis  Alternative hypothesis that PCOS is due to intrinsic ovarian dysfunction. This hypothesis considers that primary functional ovarian hyperandrogenism (FOH) is the essence of PCOS.  The intraovarian level of androgens in FOH is higher than in most adrenal causes of androgen excess and results in excessive growth of small ovarian follicles while inhibiting follicular maturation and development of the dominant follicle.  These result in the polycystic appearance of the ovary and the anovulatory symptoms.
  • 105. Extrinsic factors Contributing to Dysregulated Steroidogenesis  The insulin/insulin-like growth factors (IGF) system is capable of acting in synergy with trophic hormones, contributing to ovarian or adrenal excess androgen production.  In the ovary, insulin acts in conjunction with LH to enhance androgen production and reverse the LH- induced down-regulation of LH binding sites. Insulin and IGFs increase the activities of multiple steroidogenic enzymes in both the ovaries and adrenal glands.  This suggests that the hyperandrogenemia and obesity of PCOS are mechanistically linked.
  • 106. Treatment for PCOS in adolescents is directed at the following clinical manifestations: Menstrual irregularity Cutaneous hyperandrogenism, primarily hirsutism and acne Obesity and insulin resistance
  • 107. TREATMENT FOR PCOS Menstrual irregularity should be treated in adolescents with PCOS because chronic anovulation increases the risk of developing endometrial hyperplasia, which is associated with endometrial carcinoma. In addition, anemia can result from dysfunctional uterine bleeding or menorrhagia.
  • 108. TREATMENT FOR PCOS  The combination oral contraceptive pill (OCP), which contains estrogen and progestin, usually is the first-line treatment for adolescents with PCOS and menstrual irregularity, especially in patients with cutaneous signs of androgen excess.  OCPs induce regular menstrual periods with a higher degree of reliability than other forms of treatment.  Progestin inhibits endometrial proliferation, preventing hyperplasia. Estrogen inhibits the activity of the hypothalamic-pituitary-gonadal axis, reducing ovarian androgen production as well as increasing serum sex hormone binding globulin (SHBG) levels.  OCP therapy also will normalize androgen levels within 18 to 21 days.  After three months, the efficacy of treatment is assessed by evaluating clinical symptoms and androgen levels. If the treatment is effective, as a general rule, OCPs should be continued until the patient is gynecologically mature (five years postmenarcheal). 
  • 109. TREATMENT FOR PCOS Limitations — The role of OCPs in the management of PCOS in adolescents may be limited for several reasons:  OCP therapy may make weight loss more difficult to attain because it promotes salt and water retention.  The patient may believe the treatment is curative and defer a definitive diagnostic work-up.  OCPs do not permit conception if and when it is desired.  In perimenarcheal girls with short stature who have open epiphyses, OCPs are contraindicated because OCPs contain growth-inhibitory amounts of estrogen.
  • 111. OBESITY AND INSULIN RESISTANCE  The treatment of obesity improves ovulation, acanthosis nigricans, androgen excess, and cardiovascular risk in patients with PCOS.  Weight reduction is indicated in obese patients with PCOS as part of a program to reduce cardiovascular risk factors.  Diet and exercise are the first-line treatment for obese adolescents with PCOS as for obese individuals without PCOS.
  • 112. Insulin Resistance  Obesity is of major importance in the insulin resistance of PCOS, although insulin resistance is disproportionate to the degree of adiposity. Insulin resistance is commonly manifested as acanthosis nigricans  The biguanides, of which metformin is the only one available in the US are thus a potential adjunct in the treatment of PCOS; thiazolidinediones also are effective in reducing insulin levels, but have raised safety concerns, as discussed below.  Although their mechanisms of action differ, both metformin and thiazolidinediones reduce insulin concentrations, promote ovulation, and lower androgen levels  Metformin is the only one of these agents that we currently use in adolescents with PCOS because of concerns of weight gain and rare hepatic and possible cardiac toxicity with thiazolidinediones.  Randomized, placebo-controlled trials in adolescents and adults have shown that metformin significantly increases the frequency of menses and ovulation (by about 50 percent), and lowers testosterone levels (by about 20 percent).
  • 113. Pharmacologic Management Changed Amlodipine 5mg to Losartan 50mg/tab as there was no change for one month. Prevent target organ damage and decreased fluid retention 1st Follow-up April 2012
  • 114. MY USE COUNSELING/MOTIVATIONAL INTERVIEW  I once again asked the patient how she was doing. How did she feel about the diet change? I asked if she was fully aware and really understood her condition.  “ok lang” “Ginagawa ko rin dahil sa mama ko.”  I asked her if she still remembers what I told her about the health risks involved with hypertension and obesity.  She said “Opo doc, naala ko naman.”  I asked her if her overweight condition made her conscious with her appearance, she said NO during the 1st consult, but she did admitted that it started to beome a concern especially when some of her classmates teases her. She also wanted to be noticed by her crush.
  • 115. BEHAVIOR CHANGE TOOL AND DECISIONAL BALANCE TECHNIQUE  I asked her what are her goals in life.  She said she wants to work as an engineer and have a family for own. She wants to travel and meet lots of new friends.  I asked her what does eating to much and having a sedentary lifestyle has to do with her dream...  “Magkakasakit ako palagi at baka palagi nasa hospital”.
  • 116. BEHAVIOR CHANGE TOOL AND DECISIONAL BALANCE TECHNIQUE  I used the Decisional Balance technique for my patient….
  • 117. Decisional Balance  "reflects the individual's relative weighing of the pros and cons of changing.“  Decision making was conceptualized by Janis and Mann as a "decisional balance sheet" of comparative potential gains and losses.“  Decisional balance measures, the pros and the cons, have become critical constructs in the Transtheoretical Model  Sound decision making requires the consideration of the potential benefits (pros) and costs (cons) associated with a behavior's consequences.
  • 118. Decisional Balance  Decisional balance is one of the best predictors of future change. TTM research has found the following relationships between the pros, cons, and the stage of change across 48 behaviors and over 100 populations studied.  The cons of changing outweigh the pros in the Pre- contemplation stage.  The pros surpass the cons in the middle stages.  The pros outweigh the cons in the Action stage
  • 119. Decisional Balance Maintaining Current Use Changing Use Pattern Benefits Benefits Costs Costs “Masarap” “Hindi Magkakasakit” “Gaganda Ako “ “Mas Okay ang suot” “Magkakasakit ako” “Mas lalo tumaba” “Hindi na masarap”
  • 120. BEHAVIOR CHANGE TOOL AND DECISIONAL BALANCE TECHNIQUE She then realized that she would have to change. The patient is now willing to change hence I made a treatment plan to target obesity hence decreased incidence of hypertension.
  • 121. Hypertension, Metabolic Syndrome, PCOS Obesity Lifestyle modification Behavioral Change and Motivation
  • 122. Treat Obesity Improve symptoms and minimize health risks
  • 123. APPROACH ON TREATMENT TO OBESITY According the AAP’s Recommendations for Treatment of Child and Adolescent Overweight and Obesity— Comprehensive interventions that include behavioral therapy along with changes in nutrition and physical activity are the most closely studied and seem to be the most successful approaches to improving long-term weight and health status.
  • 124. APPROACH ON TREATMENT TO OBESITY  In the study…showed a guideline on how to treat and manage adolescent obesity based on 1. Nutritional Treatment 2. Macronutrient Therapy 3. Food Behaviors 4. Dietary Interventions 5. Physical Activity and Reducing Sedentary Activities 6. Behavioral Approaches 7. Other Interventions 8. Recommendations of Stages of Treatment
  • 125. APPROACH ON TREATMENT TO OBESITY Nutritional Treatment In the guideline, it reviewed nutritional treatment for our patient to decrease obesity which included:  Fruits and Vegetables  Fruit Juice  Sweetened Beverage  Dairy Food  Calcium  Dietary fiber Eight studies evaluating the relationship between fruit and/or vegetable intake and body weight were reviewed. All had mixed results but two studies found an inverse association with adiposity.
  • 126. APPROACH ON TREATMENT TO OBESITY Macronutrient Therapy Carbohydrate Fat Protein
  • 127. Glycemic index  Glycemic index (GI) has been proposed to affect body weight regulation and risk for obesity- associated complications.80 The GI is defined as the area under the glucose dose-response curve after consumption of 50 g of available carbohydrate from a test food, divided by the area under the curve after consumption of 50 g of available carbohydrate from a control food (either white bread or glucose).  Short-term feeding studies indicated that hunger and cumulative food intake were greater 3 to 5 hours after a high-GI versus low-GI meal, controlled for macronutrient and energy contents.
  • 128. FOOD BEHAVIORS In terms of the FOOD BEHAVIORS of our patient  Breakfast Skipping  Snacking  Eating Out
  • 129. DIETARY INTERVENTIONS Balanced-Macronutrient/Low-Energy Diet Salt reduced-energy diet The traffic light diet The Food Guide Pyramid
  • 130. PHYSICAL ACTIVITY It used these measurements to calculate physical activity levels, as follows: physical activity level-total energy and expenditure/basal metabolic rate.
  • 131. Amount of Physical Activity  The American Academy of Pediatrics recommends that 30 minutes of this activity occur during the school day. Very obese children may need to start with shorter periods of activity and gradually increase the time spent being active.  Reducing Sedentary Activities  Television Viewing and Obesity
  • 132. Weight Recommendations According to Age and BMI Percentile
  • 133. The AAP guideline provided a systematic approach which to manage obesity patients. The staged-care process is divided into 4 stages, that is: (1) Prevention Plus (healthy lifestyle changes) (2) Structured weight management (3) Comprehensive multidisciplinary intervention (4) tertiary care intervention.
  • 134. Weight Recommendations According to Age and BMI Percentile
  • 135. NONPHARMACOLOGIC PLAN  A. Use Prevention Plus Stage 1 Intervention  Using the algorithm, our patient is at the >99 percentile hence a Prevention Plus Stage 1 interventions should be based on the family’s readiness to change and include the following: 1. Consumption of 5 servings of fruits and vegetables per day 2. Minimization or elimination of sugar-sweetened beverages 3. Limits of 2 hours of screen time per day, no television in the room where the child sleeps, and no television viewing 4. 1 hour of physical activity per day  Physical activity can be increased gradually for sedentary children. Children may be unable to achieve 1 hour of activity per day initially but can gradually increase activity to reach 1 hour/day.
  • 136. B. Stricter implementation on the Diet Low Energy Diet of 2000kcal C350 P75 F 35 from a 3022kcal diet and a strict decrease of salt content. C. Establishing an exercise plan Jogging at their area for 40 min starting from moderate to vigorous aerobic-based physical activity 3–5 days/week. NONPHARMACOLOGIC PLAN
  • 137. My plan for Metabolic Syndrome
  • 138. My Plan for PCOS
  • 139. 2nd follow-up May 2012  S> Weight loss of 8 pounds for 2 monthS. Lessen of BP from 150/90 to 130/80… No OB consult yet.Patient was advised to take OB consult in the near future.Patient still has no menstruation. Management  Maintain medicines and continued diet and exercise plan.  Stop Losartan I also advised that their family; the parents and her brothers and sisters to seek consult for the obesity problem as well.
  • 140. 3rd Follow-up August 2012  Patient had weight loss of 2 pounds but having trouble to maintain diet and exercise during the school year due to the availability of food and temptations. BP lowered to 120/80. Patient started to play badminton with family and still continue to jog if she has free time. Plan:  Advise to have a more structured diet and exercise to adapt to school by having a list of food to eart in day. Patient was advised to have cooked food from home
  • 143. PSYCHOSOCIAL ISSUES - ADOLESCENT ISSUES Self-Image Addiction to TV and Facebook Role of parents in adolescence
  • 144. WELLNESS PLAN FOR THE PATIENT Lifestyle  Continue the Prevention Plus Plan for our patient with a advice increase Physical and outdoor activities. Screening  Patient was advised an annual screening to detect organ damage and risk of other disease like Type II Diabetes  Immunizations- Influenza vaccine yearly, Varicella vaccine.
  • 145. GOING BACK TO THE PATIENT  The good news is that the patient’s BP is at 120-130/80-90.  Patient hasn’t made substantial weight loss, but the good thing is that during the past three months her lifestyle changed dramatically when compared alongside the years that she was excessively eating. She started to gain self-confidence since the change of eating habits. The family changed their eating habits and have modified their lifestyle accordingly too.
  • 146. Insight Holistic care Interrelationship of Diseases The Importance of Lifestyle for being Healthy Counseling and Motivation Behavior change as part of being a Doctor The power of change Caring for patient is not a shot deal, have to do lots of follow-up and evaluation Importance of education and value formation in children and adults ( School and Government)
  • 147. Insight Suggestions:  Comprehensive Government Plan to Educate and Change the Lifestyle of our Youth  Insight (slide) My message to everyone…  As doctors, we are privileged to have the power to change lives. Let us go forth and use this opportunity to be an instrument towards positive change.