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KASTURI RAMASAMY1
Pre-term labour
 Labour starts before the 37th
completed week (<259 days),
counting from the first day of the
last menstrual period
 Lower limit of gestation: 20 weeks
(developed) & 28 weeks (developing
countries)
2
History
Complications in
present pregnancy
Iatrogenic
Idiopathic
Aetiology *multifactorial
 Previous history of
induced or spontaneous
abortion or preterm
delivery
 Pregnancy following
assisted reproductive
techniques (ART)
 Asymptomatic bacteriuria
or recurrent UTI
 Low socio-economic &
nutritional status
 Maternal stress
Maternal
Pregnancy complications –pre
eclampsia, antepartum
haemorrhage, PROM,
polyhydramnios
Uterine anomalies –cervical
incompetence, malformations of
uterus
Medical & surgical illness –acute fever, acute
pyelonephritis, diarrhoea, acute appendicitis,
toxoplasmosis, abdominal operation.
*hypertension, nephritis, severe anaemia,
diabetes, decompensated heart lesion, low BMI
Genital tract infection –bacterial vaginosis,
beta haemolytic streptococcus, bacteroides,
chlamydia, mycoplasma
Fetal
Multiple pregnancy,
congenital anomalies,
IUD
Placental
Infarction,
thrombosis, placenta
previa or abruption
Indicated preterm delivery d/t medical or
obstetric conditions
Idiopathic(Majority): Premature effacement of the
cervix with irritable uterus & early engagement of the
head
3
Aetiopathogenesis
4
Diagnosis
Regular uterine
contractions with or
without pain (at least 1
every 10 minutes)
Dilatation (≥2 cm) and
effacement (80%) of
cervix
Length of cervix
(measured by TVS)
≤2.5 cm and
funnelling of the
internal os
Pelvic pressure ,
backache or vaginal
discharge or bleeding
6
Predictors
Clinical
Multiple pregnancy
H/O preterm birth
Genital tract infection
Symptoms of PTL
Biophysical
Uterine contractions ≥
4/hr
Bishop score ≥ 4
Cervical length (TVS) ≤
2.5cm
Biochemical
Fetal fibronectin (fFN)
in cervicovaginal
discharge
Others: IL-6, IL-8,
TNF-a
7
Management
 Principles
1) Prevent the preterm onset of labour, if possible
2) Arrest preterm labour if not contraindicated
3) Appropriate management of labour
4) Effective neonatal care
8
1. Prevention of PTL
 Primary care : Reducing high risk factors.
 Secondary care : Screening tests for early detection and prophylactic
treatment. (tocolytics)
 Tertiary care : Reduce perinatal morbidity & mortality after diagnosis
(corticosteroids)
Investigations
• FBC
• Urinalysis and C&S
• Cervicovaginal swab –culture & fibronectin
• USG –fetal wellbeing, cervical length & placental localisation
• Serum electrolytes and glucose levels ( for tocolytics usage)
9
2. Measures to arrest PTL
 Only in negligible proportion of
cases
Bed rest (left lateral)
Adequate hydration
Prophylactic antibiotics –not routinely
given
Prophylactic cervical cerclage *
Tocolytic agents Short term therapy
• To delay delivery for at least 48 hours for glucocorticoid
therapy to enhance fetal lung maturation
• In utero transfer of patient >> advanced NICU
For cervical incompetence
–reinforces the weak cervix by non-
absorbable tape, placed around the
cervix at the level of internal os
1. Shirodkar’s operation
2. Mc Donald’s operation
• Fetus is not compromised
• Maternal conditions remain good
• Intact membranes
10
2. Measures to arrest PTL
CONTRAINDICATIONS
• Uncontrolled DM
• Thyrotoxicosis
• Severe HTN
• Cardiac disease
• Hemorrhage in pregnancy
Maternal
• Fetal distress
• Fetal death
• Congenital malformation
• Pregnancy > 34 weeks
Fetal
• ROM
• Chorioamnionitis
• Cervical dilatation > 4cm
Others
Glucocorticoid
 < 34 weeks
 Minimize RDS, IVH & NEC
 Benefit persists as long as 18 days
 Betamethasone* 12mg IM 24 hours apart 2
doses OR
 Dexamethasone 6 mg IM every 12 hours for 4
doses
Risks:
 PROM (~infection)
 Insulin dependent DM needs insulin readjustment
 Transient reduction of fetal breathing and body
movements
11
3. Management of labor in PTL
*prevent birth asphyxia, RDS
*prevent birth trauma (duration of labour : short)
FIRST STAGE SECOND STAGE
1. Patient is put to bed [to prevent PPROM]
1. The birth should be gentle and slow [to avoid
compression & decompression of the head]
2. Oxygen mask to mother [Adequate fetal
oxygenation]
2. Episiotomy may be done [to minimise head
compression d/t perineal resistance]
3. Epidural analgesia of choice. 3. Tendency to delay is curtailed by low forceps.
4. Monitor the labour carefully by using continuous
Electronic Fetal Monitoring (EFM).
4. The cord is to be clamped immediately [prevent
hypervolemia & hyperbilirubinemia]
5. C-section only if indicated.
5. Shift baby > NICU
6. NICU for good outcome.
12
Principle management of PTL
Glucocorticoids • Reduce neonatal RDS, IVH, NEC
Antenatal
transfer
• NICU
Tocolytics drugs • For short period (48 hours)
Antibiotics
• Prevent infection by Group B streptococcus
[GBS]
Careful
intrapartum
monitoring
• Minimal trauma, neonatologist
Vaginal delivery • Otherwise –indications for C-section
13
Premature Rupture of Membranes
(PROM)
 Spontaneous rupture of the membranes any time
beyond 28th week of pregnancy but before the onset
of labour
 > 37 completed weeks : term
 < 37 weeks of gestation: pre term
 Rupture of membranes > 24 hours before delivery :
prolonged rupture of membrane
 10% of all pregnancies
14
PROM
-causes
Increased friability
of the membranes
Decreased tensile
strength of the
membranes
Polyhydramnios
Cervical
incompetence
Multiple pregnancy
Infection
chorio-amnionitis,
UTI, lower genital
tract infection*
Cervical length
< 2.5cm
Prior Pre-term
Labor
Low BMI
(<19 kg/m2)
15
PROM
-diagnosis
Escape of watery
discharge per vaginum;
gush or slow leak.
Differential
diagnosis
• Hydrorrhoea
gravidarum [periodic
watery discharge occurs
probably d/t excessive
decidual glandular
secretion]
• Incontinence of urine
16
PROM
-confirmation of diagnosis
Inspect liquor
escaping out
through cervix
Speculum
examination
pH detection
[Lithmus /Nitrazine
paper]
Ferning pattern on
smearing
Orange blue
colouration of cells
(centrifuged cells
stained with 0.1%
Nile blue sulphate)
Vaginal pool
examination
(fluid from
posterior
fornix) Support diagnosis
+ assess fetal well
being
USG
 pH 6-6.2 [Normal vaginal pH
during pregnancy is 4.5-5.5;
liquor amnii is 7-7.5]
 Nitrazine paper: Yellow  Blue
at pH >6
Exfoliated fat containing
cells from sebaceous
glands of the fetus
17
PROM
INVESTIGATIONS DANGERS
1. FBC
2. Urinalysis and culture
3. High vaginal swab – culture
4. Vaginal pool : Estimation of
phosphatidyl glycerol and L:S ratio
5. USG : Fetal biophysical profile
6. CTG
1) Term PROM, labour starts in 80-90%
cases within 24 hours  PTL &
prematurity
2) Ascending infection is more (if labour
fails to start within 24 hours)
~choriamnionitis
3) Cord prolapse -malpresentation
4) Dry labour d/t continuous escape of
liquor
5) Placental abruption
6) Fetal pulmonary hypoplasia
7) Neonatal sepsis, RDS, IVH, NEC
8) Perinatal morbidities (cerebral palsy)
18
PROM
-preliminaries
1. Aseptic examination [to confirm the diagnosis, assess the state of cervix, to detect any cord
prolapse]
2. Avoid vaginal digital speculum
3. Patient is put to bed rest + sterile vulval pad is applied [to observe any further
leakage]
Diagnosis is confirmed, management depends on:
a) Gestational age of fetus
b) In labor or not
c) Sepsis evidence
d) Fetal survival
*monitor maternal pulse, temperature & FHR for 4 hourly
19
PROM
Term
• Watch carefully (if not in
labour)
• Usually starts within 24
hours. If not > induce by
oxytocin.
• C-section if indicated.
Preterm
• Balance risk of infection
vs prematurity. *NICU
Antibiotics
Ampicillin, amoxicillin or
erythromycin for 48 hours
followed by oral therapy
for 5 days or until delivery
Corticosteroids
Controversial as PROM
may accelerate fetal lung
maturation
* Combined both reduced
risk of RDS, IVH & NEC
Gestational age > 34 weeks: Infection >>
perinatal mortality d/t prematurity
20
21
THANK YOU
 Reference:
 DC Dutta Obstetrics
22

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Pre term & premature rupture of membranes (prom)

  • 2. Pre-term labour  Labour starts before the 37th completed week (<259 days), counting from the first day of the last menstrual period  Lower limit of gestation: 20 weeks (developed) & 28 weeks (developing countries) 2
  • 3. History Complications in present pregnancy Iatrogenic Idiopathic Aetiology *multifactorial  Previous history of induced or spontaneous abortion or preterm delivery  Pregnancy following assisted reproductive techniques (ART)  Asymptomatic bacteriuria or recurrent UTI  Low socio-economic & nutritional status  Maternal stress Maternal Pregnancy complications –pre eclampsia, antepartum haemorrhage, PROM, polyhydramnios Uterine anomalies –cervical incompetence, malformations of uterus Medical & surgical illness –acute fever, acute pyelonephritis, diarrhoea, acute appendicitis, toxoplasmosis, abdominal operation. *hypertension, nephritis, severe anaemia, diabetes, decompensated heart lesion, low BMI Genital tract infection –bacterial vaginosis, beta haemolytic streptococcus, bacteroides, chlamydia, mycoplasma Fetal Multiple pregnancy, congenital anomalies, IUD Placental Infarction, thrombosis, placenta previa or abruption Indicated preterm delivery d/t medical or obstetric conditions Idiopathic(Majority): Premature effacement of the cervix with irritable uterus & early engagement of the head 3
  • 5. Diagnosis Regular uterine contractions with or without pain (at least 1 every 10 minutes) Dilatation (≥2 cm) and effacement (80%) of cervix Length of cervix (measured by TVS) ≤2.5 cm and funnelling of the internal os Pelvic pressure , backache or vaginal discharge or bleeding 6
  • 6. Predictors Clinical Multiple pregnancy H/O preterm birth Genital tract infection Symptoms of PTL Biophysical Uterine contractions ≥ 4/hr Bishop score ≥ 4 Cervical length (TVS) ≤ 2.5cm Biochemical Fetal fibronectin (fFN) in cervicovaginal discharge Others: IL-6, IL-8, TNF-a 7
  • 7. Management  Principles 1) Prevent the preterm onset of labour, if possible 2) Arrest preterm labour if not contraindicated 3) Appropriate management of labour 4) Effective neonatal care 8
  • 8. 1. Prevention of PTL  Primary care : Reducing high risk factors.  Secondary care : Screening tests for early detection and prophylactic treatment. (tocolytics)  Tertiary care : Reduce perinatal morbidity & mortality after diagnosis (corticosteroids) Investigations • FBC • Urinalysis and C&S • Cervicovaginal swab –culture & fibronectin • USG –fetal wellbeing, cervical length & placental localisation • Serum electrolytes and glucose levels ( for tocolytics usage) 9
  • 9. 2. Measures to arrest PTL  Only in negligible proportion of cases Bed rest (left lateral) Adequate hydration Prophylactic antibiotics –not routinely given Prophylactic cervical cerclage * Tocolytic agents Short term therapy • To delay delivery for at least 48 hours for glucocorticoid therapy to enhance fetal lung maturation • In utero transfer of patient >> advanced NICU For cervical incompetence –reinforces the weak cervix by non- absorbable tape, placed around the cervix at the level of internal os 1. Shirodkar’s operation 2. Mc Donald’s operation • Fetus is not compromised • Maternal conditions remain good • Intact membranes 10
  • 10. 2. Measures to arrest PTL CONTRAINDICATIONS • Uncontrolled DM • Thyrotoxicosis • Severe HTN • Cardiac disease • Hemorrhage in pregnancy Maternal • Fetal distress • Fetal death • Congenital malformation • Pregnancy > 34 weeks Fetal • ROM • Chorioamnionitis • Cervical dilatation > 4cm Others Glucocorticoid  < 34 weeks  Minimize RDS, IVH & NEC  Benefit persists as long as 18 days  Betamethasone* 12mg IM 24 hours apart 2 doses OR  Dexamethasone 6 mg IM every 12 hours for 4 doses Risks:  PROM (~infection)  Insulin dependent DM needs insulin readjustment  Transient reduction of fetal breathing and body movements 11
  • 11. 3. Management of labor in PTL *prevent birth asphyxia, RDS *prevent birth trauma (duration of labour : short) FIRST STAGE SECOND STAGE 1. Patient is put to bed [to prevent PPROM] 1. The birth should be gentle and slow [to avoid compression & decompression of the head] 2. Oxygen mask to mother [Adequate fetal oxygenation] 2. Episiotomy may be done [to minimise head compression d/t perineal resistance] 3. Epidural analgesia of choice. 3. Tendency to delay is curtailed by low forceps. 4. Monitor the labour carefully by using continuous Electronic Fetal Monitoring (EFM). 4. The cord is to be clamped immediately [prevent hypervolemia & hyperbilirubinemia] 5. C-section only if indicated. 5. Shift baby > NICU 6. NICU for good outcome. 12
  • 12. Principle management of PTL Glucocorticoids • Reduce neonatal RDS, IVH, NEC Antenatal transfer • NICU Tocolytics drugs • For short period (48 hours) Antibiotics • Prevent infection by Group B streptococcus [GBS] Careful intrapartum monitoring • Minimal trauma, neonatologist Vaginal delivery • Otherwise –indications for C-section 13
  • 13. Premature Rupture of Membranes (PROM)  Spontaneous rupture of the membranes any time beyond 28th week of pregnancy but before the onset of labour  > 37 completed weeks : term  < 37 weeks of gestation: pre term  Rupture of membranes > 24 hours before delivery : prolonged rupture of membrane  10% of all pregnancies 14
  • 14. PROM -causes Increased friability of the membranes Decreased tensile strength of the membranes Polyhydramnios Cervical incompetence Multiple pregnancy Infection chorio-amnionitis, UTI, lower genital tract infection* Cervical length < 2.5cm Prior Pre-term Labor Low BMI (<19 kg/m2) 15
  • 15. PROM -diagnosis Escape of watery discharge per vaginum; gush or slow leak. Differential diagnosis • Hydrorrhoea gravidarum [periodic watery discharge occurs probably d/t excessive decidual glandular secretion] • Incontinence of urine 16
  • 16. PROM -confirmation of diagnosis Inspect liquor escaping out through cervix Speculum examination pH detection [Lithmus /Nitrazine paper] Ferning pattern on smearing Orange blue colouration of cells (centrifuged cells stained with 0.1% Nile blue sulphate) Vaginal pool examination (fluid from posterior fornix) Support diagnosis + assess fetal well being USG  pH 6-6.2 [Normal vaginal pH during pregnancy is 4.5-5.5; liquor amnii is 7-7.5]  Nitrazine paper: Yellow  Blue at pH >6 Exfoliated fat containing cells from sebaceous glands of the fetus 17
  • 17. PROM INVESTIGATIONS DANGERS 1. FBC 2. Urinalysis and culture 3. High vaginal swab – culture 4. Vaginal pool : Estimation of phosphatidyl glycerol and L:S ratio 5. USG : Fetal biophysical profile 6. CTG 1) Term PROM, labour starts in 80-90% cases within 24 hours  PTL & prematurity 2) Ascending infection is more (if labour fails to start within 24 hours) ~choriamnionitis 3) Cord prolapse -malpresentation 4) Dry labour d/t continuous escape of liquor 5) Placental abruption 6) Fetal pulmonary hypoplasia 7) Neonatal sepsis, RDS, IVH, NEC 8) Perinatal morbidities (cerebral palsy) 18
  • 18. PROM -preliminaries 1. Aseptic examination [to confirm the diagnosis, assess the state of cervix, to detect any cord prolapse] 2. Avoid vaginal digital speculum 3. Patient is put to bed rest + sterile vulval pad is applied [to observe any further leakage] Diagnosis is confirmed, management depends on: a) Gestational age of fetus b) In labor or not c) Sepsis evidence d) Fetal survival *monitor maternal pulse, temperature & FHR for 4 hourly 19
  • 19. PROM Term • Watch carefully (if not in labour) • Usually starts within 24 hours. If not > induce by oxytocin. • C-section if indicated. Preterm • Balance risk of infection vs prematurity. *NICU Antibiotics Ampicillin, amoxicillin or erythromycin for 48 hours followed by oral therapy for 5 days or until delivery Corticosteroids Controversial as PROM may accelerate fetal lung maturation * Combined both reduced risk of RDS, IVH & NEC Gestational age > 34 weeks: Infection >> perinatal mortality d/t prematurity 20
  • 20. 21
  • 21. THANK YOU  Reference:  DC Dutta Obstetrics 22