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Associate Clinical. Prof. Dr Aisha M EL- Bareg, MD, PhD
Senior Consultant Obs& Gyn
Faculty of Medicine, Misurata University, Libya
13/08/201711:33‫م‬ 1‫علما‬ ‫زدنى‬ ‫ربى‬ ‫وقل‬
Prematurity
 Prematurity is the leading cause of death
in about 75 - 80 % of all non anomalous
neonatal deaths.
 The survival rate in the best neonatal
centre in the world is 97 % at birth weight
1500 grams & 75 % at birth weight 1000
grams .
Pre-term labor (PTL)
 Definition: labor starting after the age of
viability (24 weeks) and before completed 37
weeks of GA.
 Incidence
 5-10% of live birth
 Causes 80% of perinatal morbidity and
mortality.
PTL
Spontaneous
75%
Induced
25%
Etiology (risk factors)
1. Maternal causes
a. Maternal characteristics
 Black , low SES
 Poor nutrition, smoking
 Low prepregnancy wt (BMI<19.6)
 < 18yrs, > 35yrs
 Sternous work, high level of personal
stress
 Poor ANC
b. Maternal disease
All maternal diseases- Miscrriage, PTL
c. Obstetric conditions
 Previous history of PTL  40 % recurrence
 APH = PP, AP, unexplained & recurrent
 PROM  30 % of PTL .
 Polyhydramnios
 Chorioamnionitis with or without ROM
 Oligohydramnios and IUGR.
Etiology (risk factors)
d. Uterine abnormalities
 Congenital uterine malformations- 25-50%
(Müllerian fusion defects)
 Cx incompetence- cx length <2.5mm
 Submucous fibroid
 Foreign body as IUCD
 Trauma to the uterus
 Partial Asherman’s syndrome
Etiology (risk factors)
2. Fetal causes
 Multiple pregnancies- 10%
 CFMF or IUFD
 Rh isoimmunization
4. Infection
 Systemic infection- UTI, periodontal dis.
 Local infection- GBS, bacterial vaginosis
 Cx Softening & dilatation, ROM
 Release of PG- stimulate uterine contraction
Etiology (risk factors)
5. Idiopathic- >30% no detectable cause
6. Induced
 Compromised mother or fetus
Etiology (risk factors)
3. Iatrogenic
 ECV, amniocentesis
 Surgery during pregnancy
 Inducing labour- wrong date
 Ovulation induction & ART
Complications
 Neonatal complications
 Respiratory distress syndrome
(RDS)
 Patent ductus arteriosus
 Recurrent apnoeic attacks-
immature RC
 Neonatal jaundice-
Kernicterus
 Anemia- Fe is stored in the
last weeks
 Malnutrition
 Infection- undeveloped immune system
 Pneumonia, Umbilical stump infection
 Necrotising enterocolitis
 Birth trauma
 Intracranial hage, cephalohematoma
 Bone fracture
 Hypothermia
 Hypoglycemia, hypo Ca, hypo Mg
 Remote complication of PTL
 Retrolental fibroplasia
 Bronchopulmonary dysplasia
 Cerebral plasy and neurological deficiet
(hypoxic ischemic encephalopathy)
 Psychological- reduced bounding
 Development delay
 Poor school grading
 Vision & hearing impairment
 Family, school, social burden
Diagnosis of PTL
1. Identification of patient at risk of PTL
 History
 Examination
 Investigation
 Screening methods
2. Screening methods
a. Investigation for maternal general condition
b. Cervicovaginal fibronectin- 50ng/ml
c. Home uterine monitoring
d. Regular assessment of uterine activity
e. RegularTVS assessment of Cx length
f. High vaginal swab- bacteriology
3. Dx and evaluation of established PTL
 S & S of labour
 General and obstetric examination
 Sterile speculum examination
 Abdominal USS/Trans vaginal USS
 Digital examination
 Amniocentesis
 Transvaginal USS for cx assessment
 Cx length < 20 mm and contraction
= PTL
 Cx length 20-30 mm and contraction=
=probable PTL
 Cx length > 30mm
= PTL is very unlikely regardless of
contraction frequency
 Digital Cervical examination
1. Cx is ≥ 3 cm dilation/80% effaced
 PTL diagnosis is confirmed
 Evaulate for tocolysis
2. Cx is 2-3 cm dilation/<80% effaced
 PTL is likely but not established
 Monitor uterine contraction
 Repeat digital examination in 30-60 min
 PTL if findings changed
 If no cx change
 Send for fibronectin
 Trasvaginal cervical USS
 Amniocentesis if no PROM
 Confirm lung maturity
 Test for infections
 Fetal karyotyping
Management of PTL
1. Prophylactic (at high risk of PTL)
 Proper ANC, bed rest, avoid sexual activity
 Education of the patient about PTL
 Prophylactic tocolytics or progesterone
 Cx cerclage if indicated (all uterine causes)
 Tocolytics for any surgical operation
 Treatment of infection
2. Management of threatened PTL
 Rapid admission to hospital
Interfere before cx dilatation is 4cm
 Assessment of uterine contraction
 Assessment of cx status
 Assessment of fetal condition- BPP
 If there is ROM- manage as in ROM
 Tocolytics after exclusion CI
 Prophylactic antibiotics against
(GBS, bacterial vaginosis)
3. Management of established PTL
 Goals of treatment for PTL
 Permits 3 intervensions
↓ neonatal morbidity and mortailty
1. Antenatal maternal transfere to the
most appropriate hospital
2. Antibiotics - neonatal infection
3. Corticosteroids -RDS, ICH, others
Management of established PTL (cont.)
a. First stage
 Strict intrapartum monitoring
 Avoid heavy sedation,Vit K 10mg IM
b. Second stage
 Wide episiotomy- avoid sudden compression
& decompression- ICH
 No benefit of prophylactic forceps delivery
c. Indication of CS
 Preterm breech
 Fetal distress
 Maternal indication
 Obstetric indication
4. Management of newborn
 Admission in neonatal ICU
 Resuscitation
 Control of temperature & humidity
 Feeding- Breast, bottle, Nasogastric, IV
-Vit K & vitamines
 Prophylaxis against infection (strict aseptic
handling)
 Treatment of complication- ICH, RDS
(surfactant,Thyrotropin-releasing h)
Tocolysis &Tocolytics drugs
 Abolishing or delaying the uterine contraction
 Using Uterine muscle relaxants
 Indications and contraindications
indication CI
GA < 37 weeks > 37 weeks
Fetal life Living fetus IUFD
CFMF -VE +VE
IUGR -VE +VE
Membranes intact ROM (except for
short tocolysis
chorioamnionitis -VE +VE
CX Changes < 4cm > 4cm
indication CI
Fetal distress -VE +VE
APH -VE +VE
L/S ration < 2 > 2
EFW < 2 kg < 2 kg
Medical
disease
No disease +VE
 Goals of tocolysis
 Long term tocolysis
 To prolong pregnancy till the end of 37 weeks
(prophylactic)- progesterone.
 Short term tocolysis
 To prolong pregnancy for 48-72 hrs.
 PROM till corticosteroids enhance lung
maturity.
 PTL till referred to a hospital with NICU.
A. General Lines of tocolysis
1. Bed rest & fluids
2. Sedative and analgesia
3. Sexual abstinance
B. tocolytics- uterine muscle relaxants
1. Prostaglandin synthetase inhibitors (anitPG)
Cyclooxygenase (COX) inhibitor
NSAID (Indomethacin)
 ↓ PG synthetase → ↓ PG (PG F)
 Oral tables, rectal suppositories
 Limit the use for 48 – 72 hrs & < 32 wks
• Contraindications
 Active peptic ulcer
 Poorly controlled HTN, Asthma
 Coagulation disorders
 Impaired renal and liver function
 IUGF & oligohydramnios
 Renal anomalies
 Maternal complications
 GIT upset & ulcers
 Bleeding tendency (prolonged BT)
 Nephrotoxicity
 Fetal complications
 Premature closure of Ductus arteriosis if
used > 32 weeks → neonatal pulmonary
HTN
 Oligohydramnios- fetal oligouria
 Bleeding tendency
2. Oral B-sympathomimetics
 Stimulate B-receptors on the myometrial cells
↓
↑ Intracellular cAMP
↓
↓ Intracellular Ca concentration
↓
↓ uterine contraction
2. Oral B-sympathomimetics
 Examples –Terbutaline
- Ritodrine (Yutopar)
- salbutamol (Ventoline)
 Route- subcutaneous, intravenous, oral
2. Oral B-sympathomimetics
 Maternal Side effects
 Palpitation, tachycardia, arrhythmias
 Nausea, vomiting, headache, tremors
 Hypotension, dysnea & chest pain
 Hyperglycemia- ↑ hepatic glucogenolysis
 hyperkalemia
 Pulmonary odema especially with corticosteroids
2. Oral B-sympathomimetics
 Fetal side effect
 Tachycardia, hypoglycemia,
hypocalcemia, ileus
 Contraindications
 Cardiac disease
 Hyperthyroidism & severe anemia
 Uncontrolled DM
 Hypersensitivity to drugs
 APH
3. Calcium channel blockers
Inhibit intracellular Ca influx
↓
inhibit muscle contraction
 As effective as β mimetics
 Used when - β mimetics is contraindicated
- or not tolerated
3. Calcium channel blockers
 Nifedipine - (Epilat or Adalat)
- Sublingual then oral
 Contraindications
- Congestive HF - Aortic stenosis
- Concomittent use of B- mimetics or Mg SO4
3. Calcium channel blockers
- Side effects
- Hypotension - headache & flushing
- Nasal congesion - tachycardia
- Moycardial infarction
- No fetal side effects
4. Mg sulfate-
 Complete with Ca
 Tocolytic effect is poor
 Relatively safer then B-mimetics
5. Other tocolytics
- Oxytocin antagonist- Atosiban
- Transdermal glyceryl trinitrate
 Combined tocolytics
 Different mechanism with synergistic effect
 Reduce the dose of each agents
 Such as β sympathomimetics
+
NSAIDS
13/08/201711:33‫م‬ 43
‫وقل‬
‫ربى‬
‫زدنى‬
‫علما‬

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Prematurity for 4th year med.students

  • 1. Associate Clinical. Prof. Dr Aisha M EL- Bareg, MD, PhD Senior Consultant Obs& Gyn Faculty of Medicine, Misurata University, Libya 13/08/201711:33‫م‬ 1‫علما‬ ‫زدنى‬ ‫ربى‬ ‫وقل‬
  • 2. Prematurity  Prematurity is the leading cause of death in about 75 - 80 % of all non anomalous neonatal deaths.  The survival rate in the best neonatal centre in the world is 97 % at birth weight 1500 grams & 75 % at birth weight 1000 grams .
  • 3. Pre-term labor (PTL)  Definition: labor starting after the age of viability (24 weeks) and before completed 37 weeks of GA.  Incidence  5-10% of live birth  Causes 80% of perinatal morbidity and mortality.
  • 5. Etiology (risk factors) 1. Maternal causes a. Maternal characteristics  Black , low SES  Poor nutrition, smoking  Low prepregnancy wt (BMI<19.6)  < 18yrs, > 35yrs  Sternous work, high level of personal stress  Poor ANC
  • 6. b. Maternal disease All maternal diseases- Miscrriage, PTL c. Obstetric conditions  Previous history of PTL  40 % recurrence  APH = PP, AP, unexplained & recurrent  PROM  30 % of PTL .  Polyhydramnios  Chorioamnionitis with or without ROM  Oligohydramnios and IUGR. Etiology (risk factors)
  • 7. d. Uterine abnormalities  Congenital uterine malformations- 25-50% (Müllerian fusion defects)  Cx incompetence- cx length <2.5mm  Submucous fibroid  Foreign body as IUCD  Trauma to the uterus  Partial Asherman’s syndrome Etiology (risk factors)
  • 8. 2. Fetal causes  Multiple pregnancies- 10%  CFMF or IUFD  Rh isoimmunization 4. Infection  Systemic infection- UTI, periodontal dis.  Local infection- GBS, bacterial vaginosis  Cx Softening & dilatation, ROM  Release of PG- stimulate uterine contraction Etiology (risk factors)
  • 9. 5. Idiopathic- >30% no detectable cause 6. Induced  Compromised mother or fetus Etiology (risk factors) 3. Iatrogenic  ECV, amniocentesis  Surgery during pregnancy  Inducing labour- wrong date  Ovulation induction & ART
  • 10. Complications  Neonatal complications  Respiratory distress syndrome (RDS)  Patent ductus arteriosus  Recurrent apnoeic attacks- immature RC  Neonatal jaundice- Kernicterus  Anemia- Fe is stored in the last weeks
  • 11.  Malnutrition  Infection- undeveloped immune system  Pneumonia, Umbilical stump infection  Necrotising enterocolitis  Birth trauma  Intracranial hage, cephalohematoma  Bone fracture  Hypothermia  Hypoglycemia, hypo Ca, hypo Mg
  • 12.  Remote complication of PTL  Retrolental fibroplasia  Bronchopulmonary dysplasia  Cerebral plasy and neurological deficiet (hypoxic ischemic encephalopathy)  Psychological- reduced bounding  Development delay  Poor school grading  Vision & hearing impairment  Family, school, social burden
  • 13. Diagnosis of PTL 1. Identification of patient at risk of PTL  History  Examination  Investigation  Screening methods
  • 14. 2. Screening methods a. Investigation for maternal general condition b. Cervicovaginal fibronectin- 50ng/ml c. Home uterine monitoring d. Regular assessment of uterine activity e. RegularTVS assessment of Cx length f. High vaginal swab- bacteriology
  • 15. 3. Dx and evaluation of established PTL  S & S of labour  General and obstetric examination  Sterile speculum examination  Abdominal USS/Trans vaginal USS  Digital examination  Amniocentesis
  • 16.  Transvaginal USS for cx assessment  Cx length < 20 mm and contraction = PTL  Cx length 20-30 mm and contraction= =probable PTL  Cx length > 30mm = PTL is very unlikely regardless of contraction frequency
  • 17.  Digital Cervical examination 1. Cx is ≥ 3 cm dilation/80% effaced  PTL diagnosis is confirmed  Evaulate for tocolysis
  • 18. 2. Cx is 2-3 cm dilation/<80% effaced  PTL is likely but not established  Monitor uterine contraction  Repeat digital examination in 30-60 min  PTL if findings changed  If no cx change  Send for fibronectin  Trasvaginal cervical USS
  • 19.  Amniocentesis if no PROM  Confirm lung maturity  Test for infections  Fetal karyotyping
  • 20. Management of PTL 1. Prophylactic (at high risk of PTL)  Proper ANC, bed rest, avoid sexual activity  Education of the patient about PTL  Prophylactic tocolytics or progesterone  Cx cerclage if indicated (all uterine causes)  Tocolytics for any surgical operation  Treatment of infection
  • 21. 2. Management of threatened PTL  Rapid admission to hospital Interfere before cx dilatation is 4cm  Assessment of uterine contraction  Assessment of cx status  Assessment of fetal condition- BPP  If there is ROM- manage as in ROM  Tocolytics after exclusion CI  Prophylactic antibiotics against (GBS, bacterial vaginosis)
  • 22. 3. Management of established PTL  Goals of treatment for PTL  Permits 3 intervensions ↓ neonatal morbidity and mortailty 1. Antenatal maternal transfere to the most appropriate hospital 2. Antibiotics - neonatal infection 3. Corticosteroids -RDS, ICH, others
  • 23. Management of established PTL (cont.) a. First stage  Strict intrapartum monitoring  Avoid heavy sedation,Vit K 10mg IM b. Second stage  Wide episiotomy- avoid sudden compression & decompression- ICH  No benefit of prophylactic forceps delivery
  • 24. c. Indication of CS  Preterm breech  Fetal distress  Maternal indication  Obstetric indication
  • 25. 4. Management of newborn  Admission in neonatal ICU  Resuscitation  Control of temperature & humidity  Feeding- Breast, bottle, Nasogastric, IV -Vit K & vitamines  Prophylaxis against infection (strict aseptic handling)  Treatment of complication- ICH, RDS (surfactant,Thyrotropin-releasing h)
  • 26. Tocolysis &Tocolytics drugs  Abolishing or delaying the uterine contraction  Using Uterine muscle relaxants  Indications and contraindications
  • 27. indication CI GA < 37 weeks > 37 weeks Fetal life Living fetus IUFD CFMF -VE +VE IUGR -VE +VE Membranes intact ROM (except for short tocolysis chorioamnionitis -VE +VE CX Changes < 4cm > 4cm
  • 28. indication CI Fetal distress -VE +VE APH -VE +VE L/S ration < 2 > 2 EFW < 2 kg < 2 kg Medical disease No disease +VE
  • 29.  Goals of tocolysis  Long term tocolysis  To prolong pregnancy till the end of 37 weeks (prophylactic)- progesterone.  Short term tocolysis  To prolong pregnancy for 48-72 hrs.  PROM till corticosteroids enhance lung maturity.  PTL till referred to a hospital with NICU.
  • 30. A. General Lines of tocolysis 1. Bed rest & fluids 2. Sedative and analgesia 3. Sexual abstinance
  • 31. B. tocolytics- uterine muscle relaxants 1. Prostaglandin synthetase inhibitors (anitPG) Cyclooxygenase (COX) inhibitor NSAID (Indomethacin)  ↓ PG synthetase → ↓ PG (PG F)  Oral tables, rectal suppositories  Limit the use for 48 – 72 hrs & < 32 wks
  • 32. • Contraindications  Active peptic ulcer  Poorly controlled HTN, Asthma  Coagulation disorders  Impaired renal and liver function  IUGF & oligohydramnios  Renal anomalies
  • 33.  Maternal complications  GIT upset & ulcers  Bleeding tendency (prolonged BT)  Nephrotoxicity  Fetal complications  Premature closure of Ductus arteriosis if used > 32 weeks → neonatal pulmonary HTN  Oligohydramnios- fetal oligouria  Bleeding tendency
  • 34. 2. Oral B-sympathomimetics  Stimulate B-receptors on the myometrial cells ↓ ↑ Intracellular cAMP ↓ ↓ Intracellular Ca concentration ↓ ↓ uterine contraction
  • 35. 2. Oral B-sympathomimetics  Examples –Terbutaline - Ritodrine (Yutopar) - salbutamol (Ventoline)  Route- subcutaneous, intravenous, oral
  • 36. 2. Oral B-sympathomimetics  Maternal Side effects  Palpitation, tachycardia, arrhythmias  Nausea, vomiting, headache, tremors  Hypotension, dysnea & chest pain  Hyperglycemia- ↑ hepatic glucogenolysis  hyperkalemia  Pulmonary odema especially with corticosteroids
  • 37. 2. Oral B-sympathomimetics  Fetal side effect  Tachycardia, hypoglycemia, hypocalcemia, ileus  Contraindications  Cardiac disease  Hyperthyroidism & severe anemia  Uncontrolled DM  Hypersensitivity to drugs  APH
  • 38. 3. Calcium channel blockers Inhibit intracellular Ca influx ↓ inhibit muscle contraction  As effective as β mimetics  Used when - β mimetics is contraindicated - or not tolerated
  • 39. 3. Calcium channel blockers  Nifedipine - (Epilat or Adalat) - Sublingual then oral  Contraindications - Congestive HF - Aortic stenosis - Concomittent use of B- mimetics or Mg SO4
  • 40. 3. Calcium channel blockers - Side effects - Hypotension - headache & flushing - Nasal congesion - tachycardia - Moycardial infarction - No fetal side effects
  • 41. 4. Mg sulfate-  Complete with Ca  Tocolytic effect is poor  Relatively safer then B-mimetics 5. Other tocolytics - Oxytocin antagonist- Atosiban - Transdermal glyceryl trinitrate
  • 42.  Combined tocolytics  Different mechanism with synergistic effect  Reduce the dose of each agents  Such as β sympathomimetics + NSAIDS