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WHAT YOU SHOULD HAVE READ BUT….2010 ,[object Object],University of Verona, Italy Attilio Boner
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Prescribing competence of junior doctors:  does it add up? L Kidd, Arch Dis Child 2010;95:219 ,[object Object],[object Object]
Prescribing competence of junior doctors:  does it add up? L Kidd, Arch Dis Child 2010;95:219 ,[object Object],[object Object],[object Object]
Prescribing competence of junior doctors:  does it add up? L Kidd, Arch Dis Child 2010;95:219 undergraduate training both at a national level following GMC guidance  General Medical Council. Tomorrow’s doctors. London: General Medical Council, 2003. http://www.gmc-uk.org/education/undergraduate/GMC_tomorrows_doctors.pdf
Prescribing competence of junior doctors:  does it add up? L Kidd, Arch Dis Child 2010;95:219 ,[object Object],[object Object],Example of four prescribing questions involving commonly used medicines
Prescribing competence of junior doctors:  does it add up? L Kidd, Arch Dis Child 2010;95:219 ,[object Object],[object Object],100 - 90 - 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 % junior doctors answering correctly the 4 questions 2001-2004 2007 31% 73.3%
Prescribing competence of junior doctors:  does it add up? L Kidd, Arch Dis Child 2010;95:219 ,[object Object],[object Object],100 - 90 - 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 % junior doctors answering correctly the 4 questions 2001-2004 2007 31% 73.3% Ongoing monitoring of junior doctors’ prescribing ability has demonstrated improvements which may be due to local and national training initiatives
[object Object],[object Object],[object Object],ANTIBACTERIAL MEDICATION USE DURING  PREGNANCY AND RISK OF BIRTH DEFECTS  Crider  Arch Ped Adoles Med 2009;163:978 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],ANTIBACTERIAL MEDICATION USE DURING  PREGNANCY AND RISK OF BIRTH DEFECTS  Crider  Arch Ped Adoles Med 2009;163:978 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Reassuringly,  penicillins, erythromycins , and  cephalosporins , although used commonly by pregnant women,  were not associated  with many birth defects
% children receiving  antibiotics 19.5% Intervention 40.8% Control Effect of using an interactive booklet about childhood respiratory tract infections in primary care consultations on reconsulting and antibiotic prescribing: a cluster randomised controlled trial Francis BMJ  2009;339:b2885 ,[object Object],[object Object],[object Object],p<0.001 50 – 40 – 30 – 20 – 10 – 0
% of parents who said they would seek care in the future if their child developed a similar illness 55.3% Intervention 76.4% Control Effect of using an interactive booklet about childhood respiratory tract infections in primary care consultations on reconsulting and antibiotic prescribing: a cluster randomised controlled trial Francis BMJ  2009;339:b2885 80 – 60 – 40 – 20 – 0 ,[object Object],[object Object],[object Object],OR  =0.34
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[object Object],[object Object],[object Object],EFFECTS OF EARLY CHILDHOOD LEAD EXPOSURE ON ACADEMIC PERFORMANCE AND BEHAVIOUR OF SCHOOL AGE CHILDREN  Chandramouli   Arch Dis Child 2009;94:844
[object Object],[object Object],[object Object],EFFECTS OF EARLY CHILDHOOD LEAD EXPOSURE ON ACADEMIC PERFORMANCE AND BEHAVIOUR OF SCHOOL AGE CHILDREN  Chandramouli   Arch Dis Child 2009;94:844 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Sources of lead
[object Object],[object Object],[object Object],EFFECTS OF EARLY CHILDHOOD LEAD EXPOSURE ON ACADEMIC PERFORMANCE AND BEHAVIOUR OF SCHOOL AGE CHILDREN  Chandramouli   Arch Dis Child 2009;94:844 Effect of blood lead concentration on writing. KS1, Key Stage 1
[object Object],[object Object],[object Object],EFFECTS OF EARLY CHILDHOOD LEAD EXPOSURE ON ACADEMIC PERFORMANCE AND BEHAVIOUR OF SCHOOL AGE CHILDREN  Chandramouli   Arch Dis Child 2009;94:844 Effect of blood lead concentration on writing. KS1, Key Stage 1 Exposure to lead early in childhood has effects on subsequent educational attainment, even at blood levels below 10 µg/dl. These data suggest that the  threshold  for clinical concern should be reduced to   5 µg/dl
[object Object],SPINAL INJURY IN MOTOR VEHICLE CRASHES: ELEVATED RISK PERSISTS UP TO 12 YEARS OF AGE Brown   Arch Dis Child  2009;94:546 OR for serious spinal injury 7.1 8 – 7 – 6 – 5 – 4 – 3 – 2 – 1 – 0  IN CHILDREN AGED <12 YEARS
[object Object],SPINAL INJURY IN MOTOR VEHICLE CRASHES: ELEVATED RISK PERSISTS UP TO 12 YEARS OF AGE Brown   Arch Dis Child  2009;94:546 OR for serious spinal injury 7.1 8 – 7 – 6 – 5 – 4 – 3 – 2 – 1 – 0  ,[object Object],[object Object],IN CHILDREN AGED <12 YEARS
Abuso IL BAMBINO BATTUTO
Nonaccidental Head Injury Is the Most Common Cause of Subdural Bleeding in Infants <1 Year of Age  Matschke  Pediatrics 2009;124:1587 ,[object Object],% OF  CASES WITH SUBDURAL BLEEDING 7% 8 – 7 – 6 – 5 – 4 – 3 – 2 – 1 – 0
Nonaccidental Head Injury Is the Most Common Cause of Subdural Bleeding in Infants <1 Year of Age  Matschke  Pediatrics 2009;124:1587 % OF  CASES WITH SUBDURAL BLEEDING 82.4% 100 – 90 – 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 5.2% 8.0% NON-ACCIDENTAL HEAD INJURY OTHER CAUSES OF DEATH UNEXPLAINED CT scan
Screening for Occult Abdominal Trauma in Children With Suspected Physical Abuse  Lane  Pediatrics 2009;124:1595 % CHILDREN WHO WERE SCREENED FOR OCCULT ABDOMINAL TRAUMA 20% 30 – 20 – 10 – 0 ,[object Object],[object Object],[object Object]
Screening for Occult Abdominal Trauma in Children With Suspected Physical Abuse  Lane  Pediatrics 2009;124:1595 % CHILDREN WHO WERE SCREENED FOR OCCULT ABDOMINAL TRAUMA 30 – 20 – 10 – 0 20% Positive results were identified for 41% of those screened  ,[object Object],[object Object],[object Object]
30 – 20 – 10 – 0 OR  FOR OCCULT ABDOMINAL TRAUMA SREENING 20.4 8.5 CONSULTATION WITH THE CHILD PROTECTION TEAM ,[object Object],[object Object],CHILDREN PRESENTING WITH PROBABLE ABUSIVE HEAD TRAUMA Screening for Occult Abdominal Trauma in Children With Suspected Physical Abuse  Lane  Pediatrics 2009;124:1595
Bruising Characteristics Discriminating Physical Child Abuse From Accidental Trauma Pierce  Pediatrics 2010;125:67 ,[object Object],[object Object],[object Object],Characteristics  predictive of  abuse  were bruising on the  torso ,  ear , or  neck  for a child  ≤4 years of age  and bruising  in any region for an infant <4  months of age.
Bruising Characteristics Discriminating Physical Child Abuse From Accidental Trauma Pierce  Pediatrics 2010;125:67 Comparison of cumulative numbers of bruises for patients with abusive versus accidental trauma. Several bruises are present in case of abuse
Bruising Characteristics Discriminating Physical Child Abuse From Accidental Trauma Pierce  Pediatrics 2010;125:67 Bruise distribution for patients with abusive and accidental trauma. *  Indicates regions significantly predictive of abusive trauma * * * * * *
WHICH CLINICAL FEATURES DISTINGUISH INFLICTED FROM NONINFLICTED BRAIN INJURY?  A SYSTEMATIC REVIEW  Maguire   Arch Dis Child  2009;94:860 ,[object Object],APNOEA 17.0 p<0.001 RETINAL HEAMORRHAGE RIB  FRACTURES 20 – 15 – 10 – 5 – 0  In a child with intracranial injury OR for inflicted brain injury 3.5 p=0.03 3.03
WHICH CLINICAL FEATURES DISTINGUISH INFLICTED FROM NONINFLICTED BRAIN INJURY?  A SYSTEMATIC REVIEW  Maguire   Arch Dis Child  2009;94:860 ,[object Object],APNOEA 17.0 p<0.001 RETINAL HEAMORRHAGE RIB  FRACTURES 20 – 15 – 10 – 5 – 0  In a child with intracranial injury OR for inflicted brain injury 3.5 p=0.03 3.03 Seizures and long bone fractures were not discriminatory, and skull fracture and head/neck bruising were more associated with niBI
[object Object],[object Object],[object Object],% subjects with symptom criteria for post traumatic stress disorder 60 – 50 – 40 – 30 – 20 – 10 – 0 52.2% SCREENING FOR TRAUMATIC EXPOSURE AND POSTTRAUMATIC STRESS SYMPTOMS IN ADOLESCENTS  IN THE WAR AFFECTED EASTERN DEMOCRATIC REPUBLIC OF CONGO  Mels   Arch Ped Adoles Med 2009;163:525
SCREENING FOR TRAUMATIC EXPOSURE AND POSTTRAUMATIC STRESS SYMPTOMS IN ADOLESCENTS  IN THE WAR AFFECTED EASTERN DEMOCRATIC REPUBLIC OF CONGO  Mels   Arch Ped Adoles Med 2009;163:525 ,[object Object],[object Object]
SCREENING FOR TRAUMATIC EXPOSURE AND POSTTRAUMATIC STRESS SYMPTOMS IN ADOLESCENTS  IN THE WAR AFFECTED EASTERN DEMOCRATIC REPUBLIC OF CONGO  Mels   Arch Ped Adoles Med 2009;163:525 ,[object Object],[object Object],stupro saccheggio
FEVER CONTROL
[object Object],[object Object],[object Object],% children experiencing recurrent febrile seizure  30 – 25 – 20 – 15 – 10 – 5 – 0  23.4% ANTIPYRETIC AGENTS FOR PREVENTING RECURRENCES OF FEBRILE SEIZURES  Strengell  Arch Ped Adoles Med 2009;163:799 23.5% ANTIPIRETICS PLACEBO
ANTIPYRETIC AGENTS FOR PREVENTING RECURRENCES OF FEBRILE SEIZURES  Strengell  Arch Ped Adoles Med 2009;163:799 ,[object Object],[object Object],[object Object],% children experiencing recurrent febrile seizure  30 – 25 – 20 – 15 – 10 – 5 – 0  23.4% 23.5% ANTIPIRETICS PLACEBO Fever was  significantly higher during the episodes with seizure than in those without seizure (39.7°C vs 38.9°C; difference,  p<0.001 ) and this phenomenon was  independent  of the medication given
PAIN CONTROL
[object Object],[object Object],Pediatric Pain After Ambulatory Surgery: Where's the Medication?   Fortier  Pediatrics 2009;124;e588   % CHILDREN 86% EXPERIENCING SIGNIFICANT PAIN 24% RECEIVED  0  OR JUST  1  MEDICATION DOSE ON THE 1 st  DAY AT HOME 100 – 90 – 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0
Pediatric Pain After Ambulatory Surgery: Where's the Medication?   Fortier  Pediatrics 2009;124;e588   % CHILDREN 67% EXPERIENCING SIGNIFICANT PAIN 41% RECEIVED  0  OR JUST  1  MEDICATION DOSE ON THE 3 rd  DAY AT HOME 100 – 90 – 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 ,[object Object],[object Object]
Pediatric Pain After Ambulatory Surgery: Where's the Medication?   Fortier  Pediatrics 2009;124;e588   % CHILDREN 67% EXPERIENCING SIGNIFICANT PAIN 41% RECEIVED  0  OR JUST  1  MEDICATION DOSE 100 – 90 – 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 ,[object Object],[object Object],A large proportion of children receive little analgesic medication after surgery ON THE 3 rd  DAY AT HOME
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In Utero Iron Status and Auditory Neural Maturation in Premature Infants as Evaluated by Auditory Brainstem Response  Amin  J Pediatr  2010;156:377   Bilateral monaural  a uditory  b rainstem evoked  r esponse ( ABR ) was assessed using  80-dB nHL click stimuli at a repetition rate of 29.9/seconds within 48 hours  after birth. ,[object Object],[object Object],[object Object],[object Object]
In Utero Iron Status and Auditory Neural Maturation in Premature Infants as Evaluated by Auditory Brainstem Response  Amin  J Pediatr  2010;156:377   ,[object Object],[object Object],[object Object],[object Object],infants with latent iron deficiency  had significantly  prolonged absolute wave latencies  and  decreased frequency of mature ABR waveforms  compared with the infants with normal iron status.
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Vitamin D deficiency in young children with severe acute lower respiratory infection   McNally, Ped Pul 2009;44:981 ,[object Object],[object Object],[object Object]
Vitamin D deficiency in young children with severe acute lower respiratory infection   McNally, Ped Pul 2009;44:981 ,[object Object],[object Object],[object Object],The mean  vitamin D level for the entire ALRI group was not significantly different from the control group (81 ± 40 vs. 83 ± 30 nmol/L, respectively).
Vitamin D deficiency in young children with severe acute lower respiratory infection   McNally, Ped Pul 2009;44:981 ,[object Object],[object Object],[object Object],87 49 P=0.001
Vitamin D deficiency in young children with severe acute lower respiratory infection   McNally, Ped Pul 2009;44:981 ,[object Object],[object Object],[object Object],The mean vitamin D level for the ALRI subjects admitted to the pediatric intensive care unit (49 ± 24 nmol/L) was significantly lower (p=0.001) than that observed for both control (83 ± 30 nmol/L) and ALRI subjects admitted to the general pediatrics ward (87 ± 39 nmol/L).  P=0.001 87 49
Vitamin D deficiency in young children with severe acute lower respiratory infection   McNally, Ped Pul 2009;44:981 ,[object Object],[object Object],[object Object],P=0.001 Vitamin D deficiency (<50 nmol/L) remained associated with ALRI requiring admission to pediatric intensive care unit after the inclusion of prematurity into a multivariate logistic regression model. 87 49
[object Object],[object Object],[object Object],[object Object],[object Object],Vitamin D deficiency in young children with severe acute lower respiratory infection   McNally, Ped Pul 2009;44:981
Association between serum 25-hydroxyvitamin D level and upper respiratory tract infection in the Third National Health and Nutrition Examination Survey.  Ginde AA Arch Intern Med. 2009;169:384-90. 30 – 20 – 10 – 0 24% % patients with recent URTI 25(OH)D level ng/mL < 10 10-<30 20% ≥ 30 17% P<0.001 for trend OR=1.36 OR=1.24 OR=1.0 ,[object Object],[object Object]
Association between serum 25-hydroxyvitamin D level and upper respiratory tract infection in the Third National Health and Nutrition Examination Survey.  Ginde AA Arch Intern Med. 2009;169:384-90. 30 – 20 – 10 – 0 24% % patients with recent URTI 25(OH)D level ng/mL < 10 10-<30 20% ≥ 30 17% P<0.001 for trend OR=1.36 OR=1.24 OR=1.0 ,[object Object],[object Object],The association between 25(OH)D level and URTI seemed to be stronger in individuals with asthma (OR, 5.67)   and chronic obstructive pulmonary disease (OR,  2.26).
Association between serum 25-hydroxyvitamin D level and upper respiratory tract infection in the Third National Health and Nutrition Examination Survey.  Ginde AA Arch Intern Med. 2009;169:384-90. 30 – 20 – 10 – 0 24% % patients with recent URTI 25(OH)D level ng/mL < 10 10-<30 20% ≥ 30 17% P<0.001 for trend OR=1.36 OR=1.24 OR=1.0 ,[object Object],[object Object],patients with asthma had an odds ratio of 5.67 of recent URTI with vitamin D levels ,<10 ng/ml compared with those with vitamin D levels >30 ng/ml, and for COPD the odds ratio was  2.26.
Nutritional rickets and vitamin D deficiency Association with the outcomes of childhood very severe pneumonia: A prospective cohort study   Banajeh, Ped Pul 2009;44:1207 19.9 35.2 ,[object Object],[object Object],50 – 40 – 30 – 20 – 10 – 0 37.2% 47.3% p=0.019 % circulating neutrophils ≤ 30nmol/L >30nmol/L Vitamin D levels
19.9 35.2 ,[object Object],[object Object],85.9% 89.8% Day–5 Oxigen saturation ≤ 30nmol/L >30nmol/L 90 – 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 p=0.03 Vitamin D levels Nutritional rickets and vitamin D deficiency Association with the outcomes of childhood very severe pneumonia: A prospective cohort study   Banajeh, Ped Pul 2009;44:1207
Nutritional rickets and vitamin D deficiency Association with the outcomes of childhood very severe pneumonia: A prospective cohort study   Banajeh, Ped Pul 2009;44:1207 19.9 35.2 ,[object Object],[object Object],25 – 20 – 15 – 10 – 5 – 0 20.6% 6% p=0.031 % treatment failure Vitamin D levels ≤30nmol/L rachitic non-rachitic
19.9 35.2 ,[object Object],[object Object],85.9% 89.8% ≤ 30nmol/L >30nmol/L 90 – 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 p=0.03 Vitamin D levels Nutritional rickets and vitamin D deficiency Association with the outcomes of childhood very severe pneumonia: A prospective cohort study   Banajeh, Ped Pul 2009;44:1207 Vitamin D deficiency is significantly associated with treatment outcome and significantly predicts both reduced circulating PMNs, and Day-5 hypoxemia  (SpO 2 % <88%).  Day–5 Oxigen saturation
Vitamin D Status and Cardiometabolic Risk Factors in the United States Adolescent Population Reis  Pediatrics 2009; 124:e371 ,[object Object],MEAN 25(OH) Vitamin D ng/ml BLACK MEXICAN AMERICAN WHITE 30 – 20 – 10 – 0 15.5 21.5 28 p<0.001 p<0.001
Vitamin D Status and Cardiometabolic Risk Factors in the United States Adolescent Population Reis  Pediatrics 2009; 124:e371 ,[object Object],BLACK MEXICAN AMERICAN WHITE 30 – 20 – 10 – 0 15.5 21.5 28 p<0.001 p<0.001 Low   25(OH)D  levels were strongly associated with  overweight  status and  abdominal obesity   ( P for trend.<001)  with  high  systolic  blood pressure  ( P =.02) and plasma  glucose  concentrations ( P =.01). MEAN 25(OH) Vitamin D ng/ml
In the Lowest Quartile (<15 ng/ml) vs the Highest Quartile (>26 ng/ml) OR for  2.36 LOW HIGH-DENSITY LIPOPROTEIN CHOLESTEROL HYPERTENSION HYPERGLICEMIA 4 – 3 – 2   – 1 – 0 1.54 3.88 2.54 METABOLIC SY Vitamin D Status and Cardiometabolic Risk Factors in the United States Adolescent Population Reis  Pediatrics 2009; 124:e371
[object Object],[object Object],Relationships between 25-Hydroxyvitamin D Levels and Plasma Glucose and Lipid Levels in Pediatric Outpatients   Johnson  J Pediatr 2010;156:444 Correlation between 25(OH) D level and  fasting plasma glucose
Relationships between 25-Hydroxyvitamin D Levels and Plasma Glucose and Lipid Levels in Pediatric Outpatients   Johnson  J Pediatr 2010;156:444 Correlation between 25(OH) D level and  HDL level ,[object Object],[object Object]
Relationships between 25-Hydroxyvitamin D Levels and Plasma Glucose and Lipid Levels in Pediatric Outpatients   Johnson  J Pediatr 2010;156:444 Comparison of fasting glucose, total cholesterol, HDL, triglyceride, and non-HDL levels in subjects with 25(OH)D levels greater or less than 30 ng/mL (*p=0.002; **p<0.001) ,[object Object],[object Object]
Relationships between 25-Hydroxyvitamin D Levels and Plasma Glucose and Lipid Levels in Pediatric Outpatients   Johnson  J Pediatr 2010;156:444 Comparison of fasting glucose, total cholesterol, HDL, triglyceride, and non-HDL levels in subjects with 25(OH)D levels greater or less than 30 ng/mL (*p=0.002; **p<0.001) ,[object Object],[object Object],Low 25(OH) D  levels in children and adolescents are associated with  higher plasma glucose and lower HDL  concentrations.
[object Object],[object Object],[object Object],Prevalence and Associations of 25-Hydroxyvitamin D Deficiency in US Children: NHANES 2001-2004  Kumar  Pediatrics 2009;124;e362 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 % CHILDREN 9% Deficent  (<15 mg/ml) 61% Insufficient  (15-29 mg/ml) VITAMIN D
[object Object],[object Object],[object Object],Prevalence and Associations of 25-Hydroxyvitamin D Deficiency in US Children: NHANES 2001-2004  Kumar  Pediatrics 2009;124;e362 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 % CHILDREN 9% Deficent  (<15 mg/ml) 61% Insufficient  (15-29 mg/ml) VITAMIN D Only 4% had taken 400 IU of vitamin D per day for the past 30 days.
OR   FOR VIT D DEFICIENCY (<15 ng/mL) 1.16 DRANK MILK LESS THAN ONCE A WEEK OLDER GIRLS 5 – 4 – 3 – 2   – 1 – 0 1.6 4.9 1.9 OBESE 21.9 1.9 BLACK >4 HOURS OF TELEVISION VIDEO OR COMPUTER/DAY 0.4 VITAMIN D SUPPLEMEN-TATION Prevalence and Associations of 25-Hydroxyvitamin D Deficiency in US Children: NHANES 2001-2004  Kumar  Pediatrics 2009;124;e362
[object Object],[object Object],[object Object],[object Object],[object Object],Prevalence and Associations of 25-Hydroxyvitamin D Deficiency in US Children: NHANES 2001-2004  Kumar  Pediatrics 2009;124;e362
Use of Supplemental Vitamin D Among Infants Breastfed for Prolonged Periods Taylor  Pediatrics 2010;125:105 ,[object Object],[object Object],% pediatricians recommending  vitamin D supplementation for all breastfed infants 36.4% 40 – 30 – 20 – 10 – 0
Use of Supplemental Vitamin D Among Infants Breastfed for Prolonged Periods Taylor  Pediatrics 2010;125:105 ,[object Object],[object Object],% breast fed infants for ≥6 mo supplemented with vit D 15.9% 20 – 15 - 10 – 5 - 0
Use of Supplemental Vitamin D Among Infants Breastfed for Prolonged Periods Taylor  Pediatrics 2010;125:105 ,[object Object],[object Object],% breast fed infants for ≥6 mo supplemented with vit D 15.9% 20 – 15 - 10 – 5 - 0 OD  for supplementation=7.8 if pediatricians gave advice
Use of Supplemental Vitamin D Among Infants Breastfed for Prolonged Periods Taylor  Pediatrics 2010;125:105 ,[object Object],[object Object],% advised parents who gave the supplementation to their child 44.6% 50 - 40 – 30 – 20 – 10 – 0
Serum 25-Hydroxyvitamin D Levels Among US Children Aged 1 to 11 Years: Do Children Need More Vitamin D?  Mansbach  Pediatrics 2009;124:1404 ,[object Object],[object Object],[object Object],1% 18% 69% % CHILDREN WITH <25 <50 <75 Vitamin D serum  levels nmol/L 70 – 60 - 50 - 40 - 30 – 20 – 10 – 0
Serum 25-Hydroxyvitamin D Levels Among US Children Aged 1 to 11 Years: Do Children Need More Vitamin D?  Mansbach  Pediatrics 2009;124:1404 ,[object Object],[object Object],[object Object],1% 18% 69% % CHILDREN WITH <25 <50 <75 Vitamin D serum  levels nmol/L 70 – 60 - 50 - 40 - 30 – 20 – 10 – 0 The prevalence of serum 25(OH)D levels of <75 nmol/L was higher among children aged 6 to 11 years (73%) compared with children aged 1 to 5 years (63%);  girls (71%) compared with boys (67%);  and black (92%) children.
Serum 25-Hydroxyvitamin D Levels Among US Children Aged 1 to 11 Years: Do Children Need More Vitamin D?  Mansbach  Pediatrics 2009;124:1404 ,[object Object],[object Object],[object Object],1% 18% 69% % CHILDREN WITH <25 <50 <75 Vitamin D serum  levels nmol/L 70 – 60 - 50 - 40 - 30 – 20 – 10 – 0 The American Academy of Pediatrics recommendations for vitamin D intakes of 400 IU with a 25(OH)D threshold for vitamin D sufficiency of 50 nmol/L are largely based on studies in non-Hispanic white  infants.
CARDIOLOGY
[object Object],Delayed Recognition of Initial Stroke in Children: Need for Increased Awareness  Srinivasan Pediatrics 2009;124;e227 100   – 90 – 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 MEDIAN TIME TO AIS DIAGNOSIS (HOURS) 87.9 NEONATES p=0.002 24.8 CHILDREN
% OF INPATIENTS AT THE TIME OF STROKE 60 - 50 – 40 – 30 – 20 – 10 – 0 58% Delayed Recognition of Initial Stroke in Children: Need for Increased Awareness  Srinivasan Pediatrics 2009;124;e227 ,[object Object]
Delayed Recognition of Initial Stroke in Children: Need for Increased Awareness  Srinivasan Pediatrics 2009;124;e227
Kawasaki Disease at the Extremes of the Age Spectrum  Manlhiot  Pediatrics 2009; 124:e410 ,[object Object],[object Object],% children <0.5 4% 8% 19% 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 62% 6% 0.5-1 1-4 5-9 >9 Years at Diagnosis
Kawasaki Disease at the Extremes of the Age Spectrum  Manlhiot  Pediatrics 2009; 124:e410 ,[object Object],[object Object],% children <0.5 4% 8% 19% 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 62% 6% 0.5-1 1-4 5-9 >9 Years at Diagnosis Patients <1 year of age and those >9 years of age were more likely to have coronary artery abnormalities
Kawasaki Disease at the Extremes of the Age Spectrum  Manlhiot  Pediatrics 2009; 124:e410 ,[object Object],[object Object],% children <0.5 4% 8% 19% 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 62% 6% 0.5-1 1-4 5-9 >9 Years at Diagnosis Patients at both extremes of the age spectrum were more likely to present with <4 of the classic KD features
Kawasaki Disease at the Extremes of the Age Spectrum  Manlhiot  Pediatrics 2009; 124:e410 ,[object Object],[object Object],% children <0.5 4% 8% 19% 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 62% 6% 0.5-1 1-4 5-9 >9 Years at Diagnosis Patients >9 years of age were  less likely  to receive intravenous immunoglobulin treatment
[object Object],[object Object],[object Object],Increased Detection Rate of Kawasaki Disease Using New Diagnostic Algorithm, Including Early Use of Echocardiography  T Heuclin,  J Ped 2009;155;695 had incomplete KD  met the classic case definition KD uncertain, but successfully treated for it n° children 30 – 20 – 10 – 0 26 7 6
[object Object],[object Object],[object Object],Increased Detection Rate of Kawasaki Disease Using New Diagnostic Algorithm, Including Early Use of Echocardiography  T Heuclin,  J Ped 2009;155;695 had incomplete KD  met the classic case definition KD uncertain, but successfully treated for it n° children 30 – 20 – 10 – 0 26 7 6 Cardiac ultrasound scanning was helpful in the diagnosis of 6 of 7 patients with incomplete KD
Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Statement of American Heart Association  Newburger Pediatrics 2004;114:1708 Classic clinical criteria of Kawasaki Disease Fever persisting at least 5 days Presence of at least 4 principal features: 1) Changes in extremities Acute: Erythema of palms, soles; edema of hands, feet Subacute: Periungual peeling of fingers, toes in weeks 2 and 3 2) Polymorphous exanthem 3) Bilateral bulbar conjunctival injection without exudate 4) Changes in lips and oral cavity: Erythema, lips cracking, strawberry tongue, diffuse injection of oral and pharyngeal  mucosae 5) Cervical lymphadenopathy (1.5-cm diameter), usually unilateral
Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Statement of American Heart Association  Newburger Pediatrics 2004;114:1708 Classic clinical criteria of Kawasaki Disease Fever persisting at least 5 days Presence of at least 4 principal features: 1) Changes in extremities Acute: Erythema of palms, soles; edema of hands, feet Subacute: Periungual peeling of fingers, toes in weeks 2 and 3 2) Polymorphous exanthem 3) Bilateral bulbar conjunctival injection without exudate 4) Changes in lips and oral cavity: Erythema, lips cracking, strawberry tongue, diffuse injection of oral and pharyngeal  mucosae 5) Cervical lymphadenopathy (1.5-cm diameter), usually unilateral Patients with fever of at least 5 days and < 4 principal criteria can be diagnosed with Kawasaki disease when coronary artery abnormalities are detected by  2-dimensional echocardiography or angiography.
Laboratory findings in acute Kawasaki disease *  (Thrombocytopenia in sone infants) *
Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association. Newburger JW, Pediatrics. 2004 Dec;114:1708-33.
Refractory pneumonia and high fever Falcini,  Lancet 2010;373:1818 ,[object Object],[object Object],[object Object],[object Object],[object Object]
Refractory pneumonia and high fever Falcini,  Lancet 2010;373:1818 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Refractory pneumonia and high fever Falcini,  Lancet 2010;373:1818 (A) Frontal view showing marked pleural effusion on the right.  (B) After therapy with IVIg and methylprednisolone
Refractory pneumonia and high fever Falcini,  Lancet 2010;373:1818 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Nonresolving pneumonia and rash in an adult: pulmonary involvements in Kawasaki's disease   Ugi  ERJ  2010;35:452  ,[object Object],[object Object],[object Object],[object Object]
Nonresolving pneumonia and rash in an adult: pulmonary involvements in Kawasaki's disease   Ugi  ERJ  2010;35:452  ,[object Object],[object Object],[object Object]
Nonresolving pneumonia and rash in an adult: pulmonary involvements in Kawasaki's disease   Ugi  ERJ  2010;35:452  ,[object Object],[object Object]
Nonresolving pneumonia and rash in an adult: pulmonary involvements in Kawasaki's disease   Ugi  ERJ  2010;35:452  ,[object Object],[object Object],Based on the assumption of progressive, therapy was piperacillin/tazobactam and clarithromycin.
Nonresolving pneumonia and rash in an adult: pulmonary involvements in Kawasaki's disease   Ugi  ERJ  2010;35:452  ,[object Object],[object Object],[object Object]
Nonresolving pneumonia and rash in an adult: pulmonary involvements in Kawasaki's disease   Ugi  ERJ  2010;35:452  ,[object Object],[object Object],[object Object],The next diagnostic step would  have been bronchoscopy including bronchoalveolar lavage.
Nonresolving pneumonia and rash in an adult: pulmonary involvements in Kawasaki's disease   Ugi  ERJ  2010;35:452  ,[object Object],[object Object],[object Object]
200 – 150 – 100 – 50 – 0 ,[object Object],[object Object],[object Object],[object Object],Colesterol (mg/dL) Kawasaki Atherosclerosis in Survivors of Kawasaki Disease M Gupta-Malhotra,  J Ped 2009;155;572 control 175 mg 157 mg P=0.034
100 – 75 – 50 – 25 – 0 ,[object Object],[object Object],[object Object],[object Object],Apolipoprotein B (mg/mL) Kawasaki Atherosclerosis in Survivors of Kawasaki Disease M Gupta-Malhotra,  J Ped 2009;155;572 control 78 mg 65 mg P=0.004
100 – 75 – 50 – 25 – 0 ,[object Object],[object Object],[object Object],[object Object],Apolipoprotein B (mg/mL) Kawasaki Atherosclerosis in Survivors of Kawasaki Disease M Gupta-Malhotra,  J Ped 2009;155;572 control 78 mg 65 mg P=0.004 Small but significant differences in cholesterol and apolipoprotein B levels could suggest increased  future risk for atherosclerosis
[object Object],[object Object],[object Object],[object Object],Atherosclerosis in Survivors of Kawasaki Disease M Gupta-Malhotra,  J Ped 2009;155;572
Early Life Origins of Low-Grade Inflammation and Atherosclerosis Risk in Children and Adolescents Idoia Labayen, J  Ped 2009;155:673 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Early Life Origins of Low-Grade Inflammation and Atherosclerosis Risk in Children and Adolescents Idoia Labayen, J  Ped 2009;155:673 ,[object Object],[object Object]
Simple Table to Identify Children and Adolescents Needing Further Evaluation of Blood Pressure  Kaelber  Pediatrics 2009;123:e972 ,[object Object],[object Object]
Preventing Surgical-Site Infections in Nasal Carriers of  Staphylococcus aureus  Lonneke G.M. Bode. NEJM 2010 (362): 9-17 Background   Nasal carriers of  Staphylococcus aureus   are at increased   risk  for health care–associated infections  with this organism.   Decolonization of nasal and extranasal sites  on hospital admission   may reduce this risk.
[object Object],[object Object],[object Object],10 – 9 – 8 – 7 – 6 – 5 – 4 – 3 – 2 – 1 – 0 3.4% 7.7% Rate of  S. aureus  infection  mupirocin–chlorhexidine group placebo  group RR=0.42 p=0,008 Preventing Surgical-Site Infections in Nasal Carriers of  Staphylococcus aureus  Lonneke G.M. Bode. NEJM 2010;362:9-17
[object Object],[object Object],[object Object],10 – 9 – 8 – 7 – 6 – 5 – 4 – 3 – 2 – 1 – 0 3.4% 7.7% Rate of  S. aureus  infection  mupirocin–chlorhexidine group placebo  group RR=0.42 p=0,008 Preventing Surgical-Site Infections in Nasal Carriers of  Staphylococcus aureus  Lonneke G.M. Bode. NEJM 2010;362:9-17 The effect of  mupirocin–chlorhexidine treatment   was most pronounced for  deep surgical-site infections  (relative   risk = 0.21)
[object Object],[object Object],[object Object],10 – 9 – 8 – 7 – 6 – 5 – 4 – 3 – 2 – 1 – 0 3.4% 7.7% Rate of  S. aureus  infection  mupirocin–chlorhexidine group placebo  group RR=0.42 p=0,008 Preventing Surgical-Site Infections in Nasal Carriers of  Staphylococcus aureus  Lonneke G.M. Bode. NEJM 2010;362:9-17 The usual therapeutic regimen  for mupirocin is  3 times daily application  for 1 week
[object Object],[object Object],[object Object],[object Object],Preventing Surgical-Site Infections in Nasal Carriers of  Staphylococcus aureus  Lonneke G.M. Bode. NEJM 2010;362:9-17
Minimizing Surgical-Site Infections  RP Wenzel, NEJM 2010 (362): 75-77   ,[object Object],[object Object],[object Object]
Minimizing Surgical-Site Infections  RP Wenzel, NEJM 2010: 362: 75-77   ,[object Object],[object Object]
Chronic fatigue syndrome
Chronic Fatigue Syndrome After Infectious Mononucleosis in Adolescents Katz  Pediatrics 2009;124:189 ,[object Object],[object Object],13% 15 – 10 – 5 – 0  7% 4% % ADOLESCENTS WHO MET THE CRITERIA FOR CHRONIC FATIGUE SYNDROME 6 12 24 MONTH POST MONONUCLEOSIS
Chronic Fatigue Syndrome After Infectious Mononucleosis in Adolescents Katz  Pediatrics 2009;124:189 ,[object Object],[object Object],13% 15 – 10 – 5 – 0  7% 4% % ADOLESCENTS WHO MET THE CRITERIA FOR CHRONIC FATIGUE SYNDROME 6 12 24 MONTH POST MONONUCLEOSIS  All 13 adolescents with chronic fatigue syndrome 24 months after infectious mononucleosis were female
Chronic Fatigue Syndrome After Infectious Mononucleosis in Adolescents Katz  Pediatrics 2009;124:189 ,[object Object],[object Object],13% 15 – 10 – 5 – 0  7% 4% % ADOLESCENTS WHO MET THE CRITERIA FOR CHRONIC FATIGUE SYNDROME 6 12 24 MONTH POST MONONUCLEOSIS  Infectious mononucleosis may be a risk factor for  chronic fatigue syndrome in adolescents
The chronic fatigue syndrome: a comprehensive approach to its definition and study.  Fukuda K, Ann Intern Med. 1994;121:953–959 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Risk Factors for Persistent Fatigue With Significant School Absence in Children and Adolescent  Robert Pediatrics 2009;124;e89 ,[object Object],[object Object],[object Object],50.6% % CHILDREN AT FOLLOW-UP 60 – 50 – 40 – 30 – 20 – 10 – 0 29.1% 20.3% PERSISTENT FATIGUE IMPROVEMENT PERSISTENT FATIGUE WITH SIGNIFICANT SCHOOL ABSENCE
2 – 1 – 0 1.4 2.1 2.0 1.8 1.7 1.8 1.9 SLEEP PROBLEMS BLURRED VISION PAIN IN ARMS OR LEGS BACK PAIN COSTIPATION MEMORY DEFICITS HOT AND COLD SPELLS OR   FOR PERSISTENCE Risk Factors for Persistent Fatigue With Significant School Absence in Children and Adolescent  Robert Pediatrics 2009;124;e89
[object Object],[object Object],[object Object],[object Object],[object Object],MEMORY AND ATTENTION PROBLEMS IN CHILDREN WITH CHRONIC FATIGUE SYNDROME OR MYALGIC ENCEPHALOPATHY  Haig-ferguson   Arch Dis Child 2009;94:757
[object Object],[object Object],[object Object],ASSOCIATION BETWEEN SCHOOL ABSENCE AND PHYSICAL FUNCTION IN PAEDIATRIC CHRONIC FATIGUE  SYNDROME/ MYALGIC ENCEPHALOPATHY  Crawley   Arch Dis Child 2009;94:752
[object Object],[object Object],ASSOCIATION BETWEEN SCHOOL ABSENCE AND PHYSICAL FUNCTION IN PAEDIATRIC CHRONIC FATIGUE  SYNDROME/ MYALGIC ENCEPHALOPATHY  Crawley   Arch Dis Child 2009;94:752
[object Object],[object Object],[object Object],% children attending ≤40% of school days 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 62% ASSOCIATION BETWEEN SCHOOL ABSENCE AND PHYSICAL FUNCTION IN PAEDIATRIC CHRONIC FATIGUE  SYNDROME/ MYALGIC ENCEPHALOPATHY  Crawley   Arch Dis Child 2009;94:752
[object Object],[object Object],[object Object],% children attending ≤40% of school days 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 62% ASSOCIATION BETWEEN SCHOOL ABSENCE AND PHYSICAL FUNCTION IN PAEDIATRIC CHRONIC FATIGUE  SYNDROME/ MYALGIC ENCEPHALOPATHY  Crawley   Arch Dis Child 2009;94:752 The factor most strongly associated with reduced school attendance was   poor physical function .  Worse physical function was associated with higher levels of  fatigue, pain and  low mood
[object Object],[object Object],[object Object],% children attending ≤40% of school days 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 62% ASSOCIATION BETWEEN SCHOOL ABSENCE AND PHYSICAL FUNCTION IN PAEDIATRIC CHRONIC FATIGUE  SYNDROME/ MYALGIC ENCEPHALOPATHY  Crawley   Arch Dis Child 2009;94:752 We found no evidence that school attendance was associated with anxiety measured either by the SCAS or the HADS
[object Object],[object Object],[object Object],2.5 – 2.0 – 1.5 – 1.0 – 0.5 – 0  2.2% FREQUENT MEDICAL ABSENCES IN SECONDARY SCHOOL STUDENTS: SURVEY AND CASE–CONTROL STUDY  Jones   Arch Dis Child 2009;94:763 % children with frequent medical absences
FREQUENT MEDICAL ABSENCES IN SECONDARY SCHOOL STUDENTS: SURVEY AND CASE–CONTROL STUDY  Jones   Arch Dis Child 2009;94:763 % children with frequent medical absences 11 – 10 – 9 – 8 – 7 – 6 – 5 – 4 – 3 – 2 – 1 – 0  8% 11% SERIOUS  ORGANIC DISEASE SYMPTOM-DEFINED SYNDROMES ,[object Object],[object Object],[object Object]
FREQUENT MEDICAL ABSENCES IN SECONDARY SCHOOL STUDENTS: SURVEY AND CASE–CONTROL STUDY  Jones   Arch Dis Child 2009;94:763 % children with frequent medical absences 11 – 10 – 9 – 8 – 7 – 6 – 5 – 4 – 3 – 2 – 1 – 0  8% 11% SERIOUS  ORGANIC DISEASE SYMPTOM-DEFINED SYNDROMES ,[object Object],[object Object],[object Object],The remainder had  physical symptoms and  minor  medical illness
FREQUENT MEDICAL ABSENCES IN SECONDARY SCHOOL STUDENTS: SURVEY AND CASE–CONTROL STUDY  Jones   Arch Dis Child 2009;94:763 % children with  psychiatric disorders CONTROLS 50 – 40 – 30 – 20 – 10 – 0  CASES p<0.001 17%   45%   ,[object Object],[object Object],[object Object]
FREQUENT MEDICAL ABSENCES IN SECONDARY SCHOOL STUDENTS: SURVEY AND CASE–CONTROL STUDY  Jones   Arch Dis Child 2009;94:763 % children with  psychiatric disorders CONTROLS 50 – 40 – 30 – 20 – 10 – 0  CASES p<0.001 17%   45%   ,[object Object],[object Object],[object Object],Only 34% with a psychiatric diagnosis had attended NHS psychiatric services
FREQUENT MEDICAL ABSENCES IN SECONDARY SCHOOL STUDENTS: SURVEY AND CASE–CONTROL STUDY  Jones   Arch Dis Child 2009;94:763 ADHD , attention deficit hyperactivity disorder;  DISC , Diagnostic Interview Schedule for Children;  OCD , obsessive compulsive disorder;  OR , odds ratio;  PTSD , post-traumatic stress disorder;  SDQ , Strengths and Difficulties Questionnaire for SDQ
Dermatology
Propranolol for Severe Infantile Hemangiomas:  Follow-Up Report  Sans   Pediatrics 2009;124:e423   ,[object Object],[object Object],[object Object],[object Object],[object Object],1)  Immediate effects on color and growth were noted in all cases. 2)  In ulcerated IHs, complete healing occurred in2 months. 3)  Objective clinical and ultrasound evidence of longer-term regression was seen in 2 months.
Propranolol for Severe Infantile Hemangiomas:  Follow-Up Report  Sans   Pediatrics 2009;124:e423   1)  Infantile hemangiomas (IHs) are the most-common soft-tissue tumors of infancy, occurring in  4% to 10% of children 1 year of age , with a clear female predominance. 2)  At birth , IHs may not be apparent or may appear as  flat  circumscribed lesions with telangiectatic vessels  on the surface.  Within the first weeks of life, IHs enter a phase of  rapid growth  with superficial and/or deep components, which lasts usually  3 to 6 months  and sometimes  up to 24 months . 3)  A period of stabilization for a few months follows, and spontaneous involution usually occurs in several years. 4) Regression is complete for 60% of  4-year-old patients and 76% of  7-year-old patients .
Propranolol for Severe Infantile Hemangiomas:  Follow-Up Report  Sans   Pediatrics 2009;124:e423   A)  10% of IHs require treatment during the proliferative phase, because of  life-threatening locations ,  local complications , or  cosmetic/functional risks . B)  IHs can be life-threatening when present in upper airways and liver, inducing acute respiratory failure and congestive heart failure, respectively. C)  Local complications such as hemorrhage, ulceration, and necrosis can be very painful and may lead to scars that are difficult to repair. D)  IHs in some locations can impair sensory functions; for example,  IHs of the upper eyelid can induce anisometropia, astigmatism, and amblyopia. IHs in other locations, such as the lip, nasal tip, or ear, may lead to permanent deformities.
Propranolol for Severe Infantile Hemangiomas:  Follow-Up Report  Sans   Pediatrics 2009;124:e423   A)  10% of IHs require treatment during the proliferative phase, because of  life-threatening locations ,  local complications , or  cosmetic/functional risks . B)  IHs can be life-threatening when present in upper airways and liver, inducing acute respiratory failure and congestive heart failure, respectively. C)  Local complications such as hemorrhage, ulceration, and necrosis can be very painful and may lead to scars that are difficult to repair. D)  IHs in some locations can impair sensory functions; for example,  IHs of the upper eyelid can induce anisometropia, astigmatism, and amblyopia. IHs in other locations, such as the lip, nasal tip, or ear, may lead to permanent deformities. We observed serendipitously that  propranolol ,  a well-tolerated, nonselective,  β -adrenergic receptor blocker  commonly used for cardiologic indications in young children, can control the growth of IHs efficiently.
Propranolol for Severe Infantile Hemangiomas:  Follow-Up Report  Sans   Pediatrics 2009;124:e423   Patient  with palpebral occlusion.   A, Palpebral occlusion at 2 months of age, after 1 week of systemic steroid treatment (2 mg/kg per day) and 1 day before treatment with propranolol.  B, Spontaneous eye reopening  after 7 days of propranolol  treatment at 2 mg/kg per day.  C, Further improvement after 2 months of propranolol treatment while prednisone treatment was tapered progressively.  D, Residual telangiectases at 12 months of age, after cessation of propranolol treatment. Time 0 7 days after 2 months  12 months
Propranolol for Severe Infantile Hemangiomas:  Follow-Up Report  Sans   Pediatrics 2009;124:e423   Patient with a painful ulcerated IH.  Standard treatment with wound care dressings and analgesics was also used. A, At 5 months of age, 1 day before treatment with propranolol. B, Beginning of healing after 2 weeks of propranolol treatment at 2 mg/kg per day. C, Limited ulceration relapse at 8 months of age, after 3 months of propranolol treatment. Complete healing was achieved after the propranolol dosage was increased to 3 mg/kg per day. After 2 weeks
Propranolol for Severe Infantile Hemangiomas:  Follow-Up Report  Sans   Pediatrics 2009;124:e423   Patient at risk of cosmetic disfigurement and ulceration because of a large IH of the inferior lip.   A, At 4 months of age, 1 day  before  treatment with propranolol. B,  After 2 months  of propranolol treatment  at 2 mg/kg per day.  C,  After 3 months  of propranolol treatment at 2 mg/kg per day.  D,  After 5 months  of propranolol treatment at 2 mg/kg per day.
Propranolol for Severe Infantile Hemangiomas:  Follow-Up Report  Sans   Pediatrics 2009;124:e423   Patient with a life-threatening laryngeal IH.  The improvement of the cutaneous component should be noted.  A, At 2 months of age,  1 day before treatment with propranolol. B, Seven days after initiation of propranolol treatment at 2 mg/kg per day, with a change in color from intense red to purple and palpable softening. C, Further improvement after 2 months of propranolol treatment at 2 mg/kg per day.  D, Residual telangiectases  at 11 months of age, 1 month after cessation of propranolol treatment.
Propranolol for Severe Infantile Hemangiomas:  Follow-Up Report  Sans   Pediatrics 2009;124:e423   α )  Propranolol is a nonselective  β -adrenergic receptor blocker. β )  Capillary endothelial cells express  β 2 -adrenergic receptors , which  modulate the release of nitric oxide, causing endothelium-dependent vasodilatation. γ )  β -Adrenergic receptor stimulation can induce modifications of signal transduction pathways  of  angiogenic factors such as VEGF or bFGF.
[object Object],[object Object],An Unusual Dermatosis in a Child  García  J Pediatr 2010;156:505
[object Object],[object Object],[object Object],An Unusual Dermatosis in a Child  García  J Pediatr 2010;156:505
An Unusual Dermatosis in a Child  García  J Pediatr 2010;156:505 ,[object Object],[object Object],[object Object],[object Object],[object Object]
Emergency Department
MAKING CHOICES: WHY PARENTS PRESENT TO THE EMERGENCY DEPARTMENT FOR NON-URGENT CARE  Williams   Arch Dis Child 2009;94:817 ,[object Object],RATED THEIR CHILD’S CONDITION AS MODERATE TO VERY SERIOUS SOUGHT ADVICE PRIOR TO ATTENDING THE EMERGENCY DEPARTMENT PRESENTED WITHIN 2-7 DAYS OF THE ONSET OF THE ILLNESS % parents 68% 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 54% 41%
Emergency Department Reliance: A Discriminatory Measure of Frequent Emergency Department Users Kroner  Pediatrics 2010;125:133 ,[object Object],[object Object],OR  for frequent use of ED 0.55 1  – 0.5 -  0 0.72 Young children Children with special health care need
Emergency Department Reliance: A Discriminatory Measure of Frequent Emergency Department Users Kroner  Pediatrics 2010;125:133 ,[object Object],[object Object],OR  for frequent use of ED 0.55 1  – 0.5 -  0 0.72 Young children Children with special health care need Whereas those with  lower education  and  low income  were more likely to have high EDR.
gastroenterology
% children with AGE treated according to guidelines 65.5% 80 – 60 – 40 – 20 – 0 The Applicability and Efficacy of Guidelines for the Management of Acute Gastroenteritis (AGE) in Outpatient Children: A Field-Randomized Trial on Primary Care Pediatricians  Albano   J Pediatr   2010;156:226   ,[object Object],[object Object],[object Object],[object Object],3% Group A Group B
% children with AGE treated according to guidelines 65.5% 80 – 60 – 40 – 20 – 0 The Applicability and Efficacy of Guidelines for the Management of Acute Gastroenteritis (AGE) in Outpatient Children: A Field-Randomized Trial on Primary Care Pediatricians  Albano   J Pediatr   2010;156:226   ,[object Object],[object Object],[object Object],[object Object],3% Group A Group B Most violations involved administration of unnecessary drugs or diets.
DURATION OF DIARRHEA (hours) 83.3 90.9 Group A Group B 100 – 80 – 60 – 40 – 20 – 0 ,[object Object],[object Object],[object Object],[object Object],The Applicability and Efficacy of Guidelines for the Management of Acute Gastroenteritis (AGE) in Outpatient Children: A Field-Randomized Trial on Primary Care Pediatricians  Albano   J Pediatr   2010;156:226   P<0.001
The Applicability and Efficacy of Guidelines for the Management of Acute Gastroenteritis (AGE) in Outpatient Children: A Field-Randomized Trial on Primary Care Pediatricians  Albano   J Pediatr   2010;156:226   The pediatricians in group A were instructed to adhere to 4 major recommendations in the guidelines:  1)  rapid oral rehydration  for 3-4 hours with hypoosmolar solution (Na 60 mmol/L);  2)  rapid refeeding after 4 hours of rehydration with the child’s normal diet, including solids, full-strength milk, or formula, with no restriction of lactose intake;  3)  avoidance of unnecessary medications;  4)  avoidance of microbiological investigations.
Prevention of Hyponatremia during Maintenance Intravenous Fluid Administration: A Prospective Randomized Study of Fluid Type versus Fluid Rate   Neville   J Pediatr   2010;156:313   Plasma sodium concentrations fell in both N/2 groups at T 8   (P < 0.01) ,[object Object],[object Object],[object Object]
Prevention of Hyponatremia during Maintenance Intravenous Fluid Administration: A Prospective Randomized Study of Fluid Type versus Fluid Rate   Neville   J Pediatr   2010;156:313   ,[object Object],[object Object],[object Object],% children with hyponatriemia at T 8 10% 40 – 30 – 20 – 10 – 0 30% NS N/2 P=0.02
[object Object],[object Object],[object Object],Prevention of Hyponatremia during Maintenance Intravenous Fluid Administration: A Prospective Randomized Study of Fluid Type versus Fluid Rate   Neville   J Pediatr   2010;156:313   % children with hyponatriemia at T 8 10% 40 – 30 – 20 – 10 – 0 30% NS N/2 P=0.02 On multiple linear regression analysis, fluid type, not rate determined risk  of hyponatremia  (P < 0.04).
Questionnaire-Based Case Finding of Celiac Disease in a Population of 8- to 9-Year-Old Children   Toftedal  Pediatrics 2010;125:e518 ,[object Object],[object Object],[object Object]
Questionnaire-Based Case Finding of Celiac Disease in a Population of 8- to 9-Year-Old Children   Toftedal  Pediatrics 2010;125:e518 ,[object Object],[object Object],[object Object],The proportion of patients with newly diagnosed CD was 1.22%  (21 of 1720).
[object Object],[object Object],[object Object],Questionnaire-Based Case Finding of Celiac Disease in a Population of 8- to 9-Year-Old Children   Toftedal  Pediatrics 2010;125:e518 A number of preclinical and  low-grade symptomatic patients with CD may be identified by their responses to a mailed questionnaire.
% children with  acute gastroenteritis at the time of gluten introduction 2.3% 1.8% CD subjects Controls ns Infectious Disease and Risk of Later Celiac Disease  in Childhood  Welander  Pediatrics 2010;125:e530  ,[object Object],[object Object],[object Object],3 – 2 – 1 – 0
% children with  acute gastroenteritis at the time of gluten introduction 2.3% 1.8% CD subjects Controls Infectious Disease and Risk of Later Celiac Disease  in Childhood  Welander  Pediatrics 2010;125:e530  ,[object Object],[object Object],[object Object],3 – 2 – 1 – 0  Parent-reported infection at the time of gluten introduction is not a major risk factor for CD. ns
The Changing Face of Childhood Celiac Disease in North America: Impact of Serological Testing  McGowan  Pediatrics 2009;124:1572 ,[object Object],[object Object],MEDIAN AGE AT DIAGNOSIS (YEARS) 2.0 9.0 PRE-TESTING TESTING 10  – 9  – 8  – 7  – 6  – 5  – 4  – 3  – 2  – 1  – 0 P<0.001
The Changing Face of Childhood Celiac Disease in North America: Impact of Serological Testing  McGowan  Pediatrics 2009;124:1572 Incidence of celiac disease  (cases per 100.000 children) 2.0 7.3 PRE-TESTING TESTING 10  – 9  – 8  – 7  – 6  – 5  – 4  – 3  – 2  – 1  – 0 P=0.03 ,[object Object],[object Object]
The Changing Face of Childhood Celiac Disease in North America: Impact of Serological Testing  McGowan  Pediatrics 2009;124:1572 FREQUENCY OF CLASSIC CELIAC DISEASE PRESENTATION 67% 19% PRE-TESTING TESTING P=0.03 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 ,[object Object],[object Object]
The Changing Face of Childhood Celiac Disease in North America: Impact of Serological Testing  McGowan  Pediatrics 2009;124:1572 In the testing group,  13 previously unrecognized clinical presentations were observed in 98 children, including ,[object Object],[object Object],[object Object]
Minutes crying  and fussing 500 – 400 – 300 – 200 – 100 – 0 YES 103 Altered Fecal Microflora and Increased Fecal Calprotectin in Infants with Colic J. Rhoads,  J Ped 2009;155;823 NO 314 colic ,[object Object],[object Object],[object Object]
Fecal calprotectin  levels mcg/g  500 – 400 – 300 – 200 – 100 – 0 YES 197 Altered Fecal Microflora and Increased Fecal Calprotectin in Infants with Colic J. Rhoads,  J Ped 2009;155;823 NO 413 colic P=0.042 ,[object Object],[object Object],[object Object]
Fecal calprotectin  levels mcg/g  500 – 400 – 300 – 200 – 100 – 0 YES 197 Altered Fecal Microflora and Increased Fecal Calprotectin in Infants with Colic J. Rhoads,  J Ped 2009;155;823 NO 413 colic P=0.042 Klebsiella species were detected in more colic patients than in control patients  (8 vs 1, P = 0.02) ,[object Object],[object Object],[object Object]
Fecal calprotectin  levels mcg/g  500 – 400 – 300 – 200 – 100 – 0 YES 197 Altered Fecal Microflora and Increased Fecal Calprotectin in Infants with Colic J. Rhoads,  J Ped 2009;155;823 NO 413 colic P=0.042 These differences could not be attributed  to differences in formula versus breast milk feeding, consumption of elemental formula,  or exposure to antibiotics ,[object Object],[object Object],[object Object]
Fecal calprotectin  levels mcg/g  500 – 400 – 300 – 200 – 100 – 0 YES 197 Altered Fecal Microflora and Increased Fecal Calprotectin in Infants with Colic J. Rhoads,  J Ped 2009;155;823 NO 413 colic P=0.042 Infants with colic,  a condition previously believed to be nonorganic in nature,  have evidence of intestinal neutrophilic infiltration and a  less diverse fecal microflora ,[object Object],[object Object],[object Object]
Fecal calprotectin  levels mcg/g  500 – 400 – 300 – 200 – 100 – 0 YES 197 Altered Fecal Microflora and Increased Fecal Calprotectin in Infants with Colic J. Rhoads,  J Ped 2009;155;823 NO 413 colic P=0.042 We plan to prospectively study the effect of treatment of children with colic with a probiotic, Lactobacillus reuteri,  in a placebo-controlled, masked investigation  to confirm previous observations  Savino, Pediatrics 2007;119:124 ,[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],Prevalence of Small Intestinal Bacterial Overgrowth  in Children with Irritable Bowel Syndrome:  A Case-Control Study   E Scarpellini, J Ped 2009;155:416 Prevalence of abnormal  LBT  ( bacterial overgrowth ) P<0.05
[object Object],[object Object],[object Object],[object Object],Prevalence of Small Intestinal Bacterial Overgrowth  in Children with Irritable Bowel Syndrome:  A Case-Control Study   E Scarpellini, J Ped 2009;155:416 P<0.05 Placebo-controlled interventional studies with  antibiotics  used to treat bacterial overgrowth are warranted to clarify the real impact of the disease on IBS symptoms Prevalence of abnormal  LBT  ( bacterial overgrowth )
Rectal Sensory Threshold for Pain is a Diagnostic Marker of Irritable Bowel Syndrome and Functional Abdominal Pain in Children U Halac,  J Ped 2010;156:60 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Rectal Sensory Threshold for Pain is a Diagnostic Marker of Irritable Bowel Syndrome and Functional Abdominal Pain in Children U Halac,  J Ped 2010;156:60
Rectal Sensory Threshold for Pain is a Diagnostic Marker of Irritable Bowel Syndrome and Functional Abdominal Pain in Children U Halac,  J Ped 2010;156:60 P<0.001 ,[object Object],[object Object],[object Object],FGID = functional gastrointestinal disease
[object Object],[object Object],[object Object],Rectal Sensory Threshold for Pain is a Diagnostic Marker of Irritable Bowel Syndrome and Functional Abdominal Pain in Children U Halac,  J Ped 2010;156:60 In children RSTP is a diagnostic marker of irritable bowel syndrome and functional abdominal pain P<0.001 FGID = functional gastrointestinal disease
Increased Auditory Startle Reflex in Children with Functional Abdominal Pain  Bakker   J Pediatr   2010;156:285   ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The multiple muscle ASR (response probability, 0% to 100%), for the 8 repetitive stimuli,  is significantly enlarged in patients with abdominal pain (n = 20) compared with control subjects (n = 23) but not compared with patients with anxiety disorder (n = 25). Increased Auditory Startle Reflex in Children with Functional Abdominal Pain  Bakker   J Pediatr   2010;156:285   The multiple muscle ASR (EMG magnitude), for the 8 repetitive stimuli, is significantly enlarged in patients with abdominal pain  (n = 20) compared with control subjects  (n = 23) but not compared with patients with anxiety (n = 25).
The multiple muscle ASR (response probability, 0% to 100%), for the 8 repetitive stimuli,  is significantly enlarged in patients with abdominal pain (n = 20) compared with control subjects (n = 23) but not compared with patients with anxiety disorder (n = 25). Increased Auditory Startle Reflex in Children with Functional Abdominal Pain  Bakker   J Pediatr   2010;156:285   The multiple muscle ASR (EMG magnitude), for the 8 repetitive stimuli, is significantly enlarged in patients with abdominal pain  (n = 20) compared with control subjects  (n = 23) but not compared with patients with anxiety (n = 25). Children with abdominal pain–related functional gastrointestinal disorders may have a generalized hypersensitivity of the central nervous system.
Recurrent Abdominal Pain in Childhood Urolithiasis  Polito  Pediatrics 2009;124:e1088 ,[object Object],% CHILDREN WITH 53% NO HISTORY OF DYSURIA OR  GROSS HEMATURIA PREVIOUSLY HOSPITALIZED  FOR ABDOMINAL SYMPTOMS 60 – 50 – 40 – 30 – 20 – 10 – 0 29% 16% PREVIOUS APPENDECTOMY
Recurrent Abdominal Pain in Childhood Urolithiasis  Polito  Pediatrics 2009;124:e1088 % children undergoing abdominal ultrasonography not showing urinary stones  2-28 mounths before the diagnosis was made 40 – 30 – 20 – 10 – 0 37% ,[object Object]
Recurrent Abdominal Pain in Childhood Urolithiasis  Polito  Pediatrics 2009;124:e1088 % children undergoing abdominal ultrasonography not showing urinary stones  2-28 mounths before the diagnosis was made 40 – 30 – 20 – 10 – 0 37% ,[object Object],69% of subjects younger than 8 years of age had central/diffuse abdominal pain.  The mean frequency of pain attacks was 4 to 9 times lower than in patients with functional or organic gastrointestinal RAP.
Recurrent Abdominal Pain in Childhood Urolithiasis  Polito  Pediatrics 2009;124:e1088 % children undergoing abdominal ultrasonography not showing urinary stones  2-28 mounths before the diagnosis was made 40 – 30 – 20 – 10 – 0 37% ,[object Object],The possibility of  urolithiasis  should be considered in children with RAP who have a  family history  of urolithiasis  and/or  infrequent pain attacks , even when dysuria and hematuria  are lacking
Rectal Fecal Impaction Treatment in Childhood Constipation: Enemas Versus High Doses Oral PEG  Bekkali  Pediatrics 2009;124:e1108 ,[object Object],[object Object],% SUCCESSFUL DISIMPACTION 80% 68% ENEMAS PEG 100 – 90 – 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 ns
Rectal Fecal Impaction Treatment in Childhood Constipation: Enemas Versus High Doses Oral PEG  Bekkali  Pediatrics 2009;124:e1108 ,[object Object],[object Object],% SUCCESSFUL DISIMPACTION 80% 68% ENEMAS PEG 100 – 90 – 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 ns Enemas and PEG were equally effective
Lactobacillus Reuteri In Infants With Functional Chronic Constipation: A Doubleblinded, Randomized, Placebo-controlled Study.  M. Martinelli J Pediatr 2010 in press ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Objectives:  To determine the benefits of  Lactobacillus rhamnosus  GG (LGG) in an extensively hydrolyzed casein formula (EHCF) in improving hematochezia and fecal calprotectin over EHCF alone. Study design:  Fecal calprotectin was compared in 30 infants with hematochezia and 4 weeks after milk elimination with that of a healthy group. We also compared fecal calprotectin and hematochezia on 26 formula-fed infants randomly assigned to EHCF with LGG (Nutramigen LGG) (EHCF + LGG) or without (Nutramigen) (EHCF - LGG) and on 4 breastfed infants whose mothers eliminated dairy. Lactobacillus  GG Improves Recovery in Infants with Blood in the Stools and Presumptive Allergic Colitis Compared with Extensively Hydrolyzed Formula Alone   Baldassarre  J Pediatr 2010;156:397
Fecal calprotectin µg/g stool 326 Hematochezia 38 Control ,[object Object],[object Object],p<0.0001 Lactobacillus  GG Improves Recovery in Infants with Blood in the Stools and Presumptive Allergic Colitis Compared with Extensively Hydrolyzed Formula Alone   Baldassarre  J Pediatr 2010;156:397 350 – 300 – 250 – 200 – 150 – 100 – 50 – 0
Lactobacillus  GG Improves Recovery in Infants with Blood in the Stools and Presumptive Allergic Colitis Compared with Extensively Hydrolyzed Formula Alone   Baldassarre  J Pediatr 2010;156:397
Decrease in fecal calprotectin µg/g stool in infants with hematochezia  after 4 week of -225  µg/g BREAST FEEDING without dairy NUTRAMIGEN ,[object Object],[object Object],Lactobacillus  GG Improves Recovery in Infants with Blood in the Stools and Presumptive Allergic Colitis Compared with Extensively Hydrolyzed Formula Alone   Baldassarre  J Pediatr 2010;156:397 0 – -50  – -100 – -200 – -250 – -112  µg/g -214  µg/g NUTRAMIGEN +  Lactobacillus GG p<0.0001
Decrease in fecal calprotectin µg/g stool in infants with hematochezia  after 4 week of -225  µg/g BREAST FEEDING NUTRAMIGEN ,[object Object],[object Object],Lactobacillus  GG Improves Recovery in Infants with Blood in the Stools and Presumptive Allergic Colitis Compared with Extensively Hydrolyzed Formula Alone   Baldassarre  J Pediatr 2010;156:397 0 – -50  – -100 – -200 – -250 – -112  µg/g -214  µg/g NUTRAMIGEN +  Lactobacillus GG p<0.0001 EHCF + LGG resulted in significant improvement of hematochezia and fecal calprotectin compared with the EHCF alone.
[object Object],[object Object],[object Object],A PRELIMINARY REPORT ON THE EFFICACY OF THE MULTICARE AR-BED IN 3-WEEK–3-MONTH-OLD INFANTS ON REGURGITATION, ASSOCIATED SYMPTOMS AND  ACID REFLUX  Vandenplas  Arch Dis Child 2010;95:26 The Multicare AR-Bed
A PRELIMINARY REPORT ON THE EFFICACY OF THE MULTICARE AR-BED IN 3-WEEK–3-MONTH-OLD INFANTS ON REGURGITATION, ASSOCIATED SYMPTOMS AND  ACID REFLUX  Vandenplas   Arch Dis Child 2010;95:26 % children who did not tolerate the 40°positioning 30 – 20 – 10 – 0  27%   ,[object Object],[object Object],[object Object]
A PRELIMINARY REPORT ON THE EFFICACY OF THE MULTICARE AR-BED IN 3-WEEK–3-MONTH-OLD INFANTS ON REGURGITATION, ASSOCIATED SYMPTOMS AND  ACID REFLUX  Vandenplas  Arch Dis Child 2010;95:26 % children with  improved ph monitoring 73%   80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 ,[object Object],[object Object],[object Object]
A PRELIMINARY REPORT ON THE EFFICACY OF THE MULTICARE AR-BED IN 3-WEEK–3-MONTH-OLD INFANTS ON REGURGITATION, ASSOCIATED SYMPTOMS AND  ACID REFLUX  Vandenplas  Arch Dis Child 2010;95:26 % children with  improved ph monitoring 73%   80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 ,[object Object],[object Object],[object Object],The mean duration of use of the Multicare AR-Bed was 3.2 months
 
[object Object]
[object Object],[object Object],% PATIENTS WHO DIED 41.6% 50 – 40 – 30 – 20 – 10 – 0 Effectiveness of Treatments for Severe Sepsis:  A Prospective, Multicenter, Observational Study   Ferrer   AJRCCM   2009:180:861
Effectiveness of Treatments for Severe Sepsis:  A Prospective, Multicenter, Observational Study   Ferrer   AJRCCM   2009:180:861  ,[object Object],[object Object],OR  FOR DEATH 0.67 P=0.008 In subjects  treated early with broad-spectrum  antibiotic  (treatment within 1 hour vs. no treatment within first 6 hours of diagnosis. 1.0 – 0.5 – 0
Association Between ICU Admission During Morning Rounds and Mortality  Afessa CHEST 2009; 136:1489 ,[object Object],[object Object],[object Object],[object Object],[object Object],% HOSPITAL MORTALITY RATE 20 – 15 – 10 – 5  – 0 16.2 % 8.8 % P<0.001 YES NO ROUND TIME OR=1.3
Association Between ICU Admission During Morning Rounds and Mortality  Afessa CHEST 2009; 136:1489 ,[object Object],[object Object],[object Object],[object Object],[object Object],% HOSPITAL MORTALITY RATE 20 – 15 – 10 – 5  – 0 16.2 % 8.8 % P<0.001 YES NO ROUND TIME OR=1.3 Most of the  round-time ICU admissions and deaths occurred in the medical ICU
Association Between ICU Admission During Morning Rounds and Mortality  Afessa CHEST 2009; 136:1489 ,[object Object],[object Object],[object Object],[object Object],[object Object],% HOSPITAL MORTALITY RATE 20 – 15 – 10 – 5  – 0 16.2 % 8.8 % P<0.001 YES NO ROUND TIME OR=1.3 Rounds may include going from one patient bed to the next, not from the sickest patient to the least sick.  This approach may result in delayed resuscitation of critically ill patients admitted to the ICU during rounds, providing a potential explanation for the increased mortality we observed in this study.
Initiation of Inappropriate Antimicrobial Therapy Results in a Fivefold Reduction of Survival in Human Septic Shock   Kumar  CHEST 2009; 136:1237 ,[object Object],80.1% % patients with appropriate antimicrobial agents 100   –  80  – 60  – 40  – 20  - 0
52% % PATIENTS SURVIVING 60 – 50 – 40 – 30 – 20 – 10 - 0 10.3% APPROPRIATE INAPPROPRIATE INITIAL T
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General paediatrics

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  • 5. Prescribing competence of junior doctors: does it add up? L Kidd, Arch Dis Child 2010;95:219 undergraduate training both at a national level following GMC guidance General Medical Council. Tomorrow’s doctors. London: General Medical Council, 2003. http://www.gmc-uk.org/education/undergraduate/GMC_tomorrows_doctors.pdf
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  • 20. Abuso IL BAMBINO BATTUTO
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  • 22. Nonaccidental Head Injury Is the Most Common Cause of Subdural Bleeding in Infants <1 Year of Age Matschke Pediatrics 2009;124:1587 % OF CASES WITH SUBDURAL BLEEDING 82.4% 100 – 90 – 80 – 70 – 60 – 50 – 40 – 30 – 20 – 10 – 0 5.2% 8.0% NON-ACCIDENTAL HEAD INJURY OTHER CAUSES OF DEATH UNEXPLAINED CT scan
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  • 27. Bruising Characteristics Discriminating Physical Child Abuse From Accidental Trauma Pierce Pediatrics 2010;125:67 Comparison of cumulative numbers of bruises for patients with abusive versus accidental trauma. Several bruises are present in case of abuse
  • 28. Bruising Characteristics Discriminating Physical Child Abuse From Accidental Trauma Pierce Pediatrics 2010;125:67 Bruise distribution for patients with abusive and accidental trauma. * Indicates regions significantly predictive of abusive trauma * * * * * *
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  • 62. In the Lowest Quartile (<15 ng/ml) vs the Highest Quartile (>26 ng/ml) OR for 2.36 LOW HIGH-DENSITY LIPOPROTEIN CHOLESTEROL HYPERTENSION HYPERGLICEMIA 4 – 3 – 2 – 1 – 0 1.54 3.88 2.54 METABOLIC SY Vitamin D Status and Cardiometabolic Risk Factors in the United States Adolescent Population Reis Pediatrics 2009; 124:e371
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  • 69. OR FOR VIT D DEFICIENCY (<15 ng/mL) 1.16 DRANK MILK LESS THAN ONCE A WEEK OLDER GIRLS 5 – 4 – 3 – 2 – 1 – 0 1.6 4.9 1.9 OBESE 21.9 1.9 BLACK >4 HOURS OF TELEVISION VIDEO OR COMPUTER/DAY 0.4 VITAMIN D SUPPLEMEN-TATION Prevalence and Associations of 25-Hydroxyvitamin D Deficiency in US Children: NHANES 2001-2004 Kumar Pediatrics 2009;124;e362
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  • 81. Delayed Recognition of Initial Stroke in Children: Need for Increased Awareness Srinivasan Pediatrics 2009;124;e227
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  • 88. Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Statement of American Heart Association Newburger Pediatrics 2004;114:1708 Classic clinical criteria of Kawasaki Disease Fever persisting at least 5 days Presence of at least 4 principal features: 1) Changes in extremities Acute: Erythema of palms, soles; edema of hands, feet Subacute: Periungual peeling of fingers, toes in weeks 2 and 3 2) Polymorphous exanthem 3) Bilateral bulbar conjunctival injection without exudate 4) Changes in lips and oral cavity: Erythema, lips cracking, strawberry tongue, diffuse injection of oral and pharyngeal mucosae 5) Cervical lymphadenopathy (1.5-cm diameter), usually unilateral
  • 89. Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Statement of American Heart Association Newburger Pediatrics 2004;114:1708 Classic clinical criteria of Kawasaki Disease Fever persisting at least 5 days Presence of at least 4 principal features: 1) Changes in extremities Acute: Erythema of palms, soles; edema of hands, feet Subacute: Periungual peeling of fingers, toes in weeks 2 and 3 2) Polymorphous exanthem 3) Bilateral bulbar conjunctival injection without exudate 4) Changes in lips and oral cavity: Erythema, lips cracking, strawberry tongue, diffuse injection of oral and pharyngeal mucosae 5) Cervical lymphadenopathy (1.5-cm diameter), usually unilateral Patients with fever of at least 5 days and < 4 principal criteria can be diagnosed with Kawasaki disease when coronary artery abnormalities are detected by 2-dimensional echocardiography or angiography.
  • 90. Laboratory findings in acute Kawasaki disease * (Thrombocytopenia in sone infants) *
  • 91. Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis, and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association. Newburger JW, Pediatrics. 2004 Dec;114:1708-33.
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  • 94. Refractory pneumonia and high fever Falcini, Lancet 2010;373:1818 (A) Frontal view showing marked pleural effusion on the right. (B) After therapy with IVIg and methylprednisolone
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  • 110. Preventing Surgical-Site Infections in Nasal Carriers of Staphylococcus aureus Lonneke G.M. Bode. NEJM 2010 (362): 9-17 Background Nasal carriers of Staphylococcus aureus are at increased risk for health care–associated infections with this organism. Decolonization of nasal and extranasal sites on hospital admission may reduce this risk.
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  • 123. 2 – 1 – 0 1.4 2.1 2.0 1.8 1.7 1.8 1.9 SLEEP PROBLEMS BLURRED VISION PAIN IN ARMS OR LEGS BACK PAIN COSTIPATION MEMORY DEFICITS HOT AND COLD SPELLS OR FOR PERSISTENCE Risk Factors for Persistent Fatigue With Significant School Absence in Children and Adolescent Robert Pediatrics 2009;124;e89
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  • 135. FREQUENT MEDICAL ABSENCES IN SECONDARY SCHOOL STUDENTS: SURVEY AND CASE–CONTROL STUDY Jones Arch Dis Child 2009;94:763 ADHD , attention deficit hyperactivity disorder; DISC , Diagnostic Interview Schedule for Children; OCD , obsessive compulsive disorder; OR , odds ratio; PTSD , post-traumatic stress disorder; SDQ , Strengths and Difficulties Questionnaire for SDQ
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  • 138. Propranolol for Severe Infantile Hemangiomas: Follow-Up Report Sans Pediatrics 2009;124:e423 1) Infantile hemangiomas (IHs) are the most-common soft-tissue tumors of infancy, occurring in 4% to 10% of children 1 year of age , with a clear female predominance. 2) At birth , IHs may not be apparent or may appear as flat circumscribed lesions with telangiectatic vessels on the surface. Within the first weeks of life, IHs enter a phase of rapid growth with superficial and/or deep components, which lasts usually 3 to 6 months and sometimes up to 24 months . 3) A period of stabilization for a few months follows, and spontaneous involution usually occurs in several years. 4) Regression is complete for 60% of 4-year-old patients and 76% of 7-year-old patients .
  • 139. Propranolol for Severe Infantile Hemangiomas: Follow-Up Report Sans Pediatrics 2009;124:e423 A) 10% of IHs require treatment during the proliferative phase, because of life-threatening locations , local complications , or cosmetic/functional risks . B) IHs can be life-threatening when present in upper airways and liver, inducing acute respiratory failure and congestive heart failure, respectively. C) Local complications such as hemorrhage, ulceration, and necrosis can be very painful and may lead to scars that are difficult to repair. D) IHs in some locations can impair sensory functions; for example, IHs of the upper eyelid can induce anisometropia, astigmatism, and amblyopia. IHs in other locations, such as the lip, nasal tip, or ear, may lead to permanent deformities.
  • 140. Propranolol for Severe Infantile Hemangiomas: Follow-Up Report Sans Pediatrics 2009;124:e423 A) 10% of IHs require treatment during the proliferative phase, because of life-threatening locations , local complications , or cosmetic/functional risks . B) IHs can be life-threatening when present in upper airways and liver, inducing acute respiratory failure and congestive heart failure, respectively. C) Local complications such as hemorrhage, ulceration, and necrosis can be very painful and may lead to scars that are difficult to repair. D) IHs in some locations can impair sensory functions; for example, IHs of the upper eyelid can induce anisometropia, astigmatism, and amblyopia. IHs in other locations, such as the lip, nasal tip, or ear, may lead to permanent deformities. We observed serendipitously that propranolol , a well-tolerated, nonselective, β -adrenergic receptor blocker commonly used for cardiologic indications in young children, can control the growth of IHs efficiently.
  • 141. Propranolol for Severe Infantile Hemangiomas: Follow-Up Report Sans Pediatrics 2009;124:e423 Patient with palpebral occlusion. A, Palpebral occlusion at 2 months of age, after 1 week of systemic steroid treatment (2 mg/kg per day) and 1 day before treatment with propranolol. B, Spontaneous eye reopening after 7 days of propranolol treatment at 2 mg/kg per day. C, Further improvement after 2 months of propranolol treatment while prednisone treatment was tapered progressively. D, Residual telangiectases at 12 months of age, after cessation of propranolol treatment. Time 0 7 days after 2 months 12 months
  • 142. Propranolol for Severe Infantile Hemangiomas: Follow-Up Report Sans Pediatrics 2009;124:e423 Patient with a painful ulcerated IH. Standard treatment with wound care dressings and analgesics was also used. A, At 5 months of age, 1 day before treatment with propranolol. B, Beginning of healing after 2 weeks of propranolol treatment at 2 mg/kg per day. C, Limited ulceration relapse at 8 months of age, after 3 months of propranolol treatment. Complete healing was achieved after the propranolol dosage was increased to 3 mg/kg per day. After 2 weeks
  • 143. Propranolol for Severe Infantile Hemangiomas: Follow-Up Report Sans Pediatrics 2009;124:e423 Patient at risk of cosmetic disfigurement and ulceration because of a large IH of the inferior lip. A, At 4 months of age, 1 day before treatment with propranolol. B, After 2 months of propranolol treatment at 2 mg/kg per day. C, After 3 months of propranolol treatment at 2 mg/kg per day. D, After 5 months of propranolol treatment at 2 mg/kg per day.
  • 144. Propranolol for Severe Infantile Hemangiomas: Follow-Up Report Sans Pediatrics 2009;124:e423 Patient with a life-threatening laryngeal IH. The improvement of the cutaneous component should be noted. A, At 2 months of age, 1 day before treatment with propranolol. B, Seven days after initiation of propranolol treatment at 2 mg/kg per day, with a change in color from intense red to purple and palpable softening. C, Further improvement after 2 months of propranolol treatment at 2 mg/kg per day. D, Residual telangiectases at 11 months of age, 1 month after cessation of propranolol treatment.
  • 145. Propranolol for Severe Infantile Hemangiomas: Follow-Up Report Sans Pediatrics 2009;124:e423 α ) Propranolol is a nonselective β -adrenergic receptor blocker. β ) Capillary endothelial cells express β 2 -adrenergic receptors , which modulate the release of nitric oxide, causing endothelium-dependent vasodilatation. γ ) β -Adrenergic receptor stimulation can induce modifications of signal transduction pathways of angiogenic factors such as VEGF or bFGF.
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  • 157. The Applicability and Efficacy of Guidelines for the Management of Acute Gastroenteritis (AGE) in Outpatient Children: A Field-Randomized Trial on Primary Care Pediatricians Albano J Pediatr 2010;156:226 The pediatricians in group A were instructed to adhere to 4 major recommendations in the guidelines: 1) rapid oral rehydration for 3-4 hours with hypoosmolar solution (Na 60 mmol/L); 2) rapid refeeding after 4 hours of rehydration with the child’s normal diet, including solids, full-strength milk, or formula, with no restriction of lactose intake; 3) avoidance of unnecessary medications; 4) avoidance of microbiological investigations.
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  • 179. Rectal Sensory Threshold for Pain is a Diagnostic Marker of Irritable Bowel Syndrome and Functional Abdominal Pain in Children U Halac, J Ped 2010;156:60
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  • 183. The multiple muscle ASR (response probability, 0% to 100%), for the 8 repetitive stimuli, is significantly enlarged in patients with abdominal pain (n = 20) compared with control subjects (n = 23) but not compared with patients with anxiety disorder (n = 25). Increased Auditory Startle Reflex in Children with Functional Abdominal Pain Bakker J Pediatr 2010;156:285 The multiple muscle ASR (EMG magnitude), for the 8 repetitive stimuli, is significantly enlarged in patients with abdominal pain (n = 20) compared with control subjects (n = 23) but not compared with patients with anxiety (n = 25).
  • 184. The multiple muscle ASR (response probability, 0% to 100%), for the 8 repetitive stimuli, is significantly enlarged in patients with abdominal pain (n = 20) compared with control subjects (n = 23) but not compared with patients with anxiety disorder (n = 25). Increased Auditory Startle Reflex in Children with Functional Abdominal Pain Bakker J Pediatr 2010;156:285 The multiple muscle ASR (EMG magnitude), for the 8 repetitive stimuli, is significantly enlarged in patients with abdominal pain (n = 20) compared with control subjects (n = 23) but not compared with patients with anxiety (n = 25). Children with abdominal pain–related functional gastrointestinal disorders may have a generalized hypersensitivity of the central nervous system.
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  • 192. Objectives: To determine the benefits of Lactobacillus rhamnosus GG (LGG) in an extensively hydrolyzed casein formula (EHCF) in improving hematochezia and fecal calprotectin over EHCF alone. Study design: Fecal calprotectin was compared in 30 infants with hematochezia and 4 weeks after milk elimination with that of a healthy group. We also compared fecal calprotectin and hematochezia on 26 formula-fed infants randomly assigned to EHCF with LGG (Nutramigen LGG) (EHCF + LGG) or without (Nutramigen) (EHCF - LGG) and on 4 breastfed infants whose mothers eliminated dairy. Lactobacillus GG Improves Recovery in Infants with Blood in the Stools and Presumptive Allergic Colitis Compared with Extensively Hydrolyzed Formula Alone Baldassarre J Pediatr 2010;156:397
  • 193.
  • 194. Lactobacillus GG Improves Recovery in Infants with Blood in the Stools and Presumptive Allergic Colitis Compared with Extensively Hydrolyzed Formula Alone Baldassarre J Pediatr 2010;156:397
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  • 209. 52% % PATIENTS SURVIVING 60 – 50 – 40 – 30 – 20 – 10 - 0 10.3% APPROPRIATE INAPPROPRIATE INITIAL T