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PRETERM LABOUR DR - ERTEQA

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PRETERM LABOUR

• Dr.ERTEQA MOHAMED
DEFINITION
• Preterm labor occurring 24w - 36w+6 days
• It is either :
Indicated preterm birth
Spontaneous preterm birth
CAUSES OF PRETERM LABOUR

1 IDIOPATHIC :70%
2.MEDICAL AND OBSTETRIC CAUSES:
• Preeclampsia. • Uterine causes :
• Placenta Previa anomaly, fibroid .
• abruptio placentae. • Cervical incompetence
• Multiple birth . • Trauma or surgery
• Polyhydramnios • Immunological disorder
as antiphospholipid Ab
• Fetal anomaly syndrome
• Fetal death. • DES exposure
• Previous second
trimester abortion or
induced abortion.
3.GENETIC FACTORS:

Genetic factor may have a role since


PTL runs in families and there is
tendency for recurrence in
subsequent pregnancy,
and have different incidence in
different races.
4.INFECTION:

Chorioaminionitis : local infection following


abnormal bacterial vaginal colonization
(bacterial vaginosis) cause local release of
prostaglandin and stimulate uterine
contractions.
Systemic infection ; as pyelonephritis is also
implicated in preterm labor ,TORCH.
5.LIFESTYLE FACTORS :
• Age less than 20 years.
• Poor nutrition.
• Poor weight gain during pregnancy.
• Low maternal pre-natal weight gain .
• Poverty.
• Smoking.
• Short stature.
• Psychological stress.
RISK AND COMPLICATIONS OF PTL

Fetal risk;
1.The risk of underlying fetal
condition e.g. :- congenital infection
or anomalies
2.Fetal intrapartum hypoxia and birth
trauma
Early neonatal risk of:
Difficulty in maintaining body temperature.
Difficulties in oral feeding.
Increased risk of infection.
Lung immaturity proportionate to the gestational
age
Congestive heart failure (PDA).
Liver immaturity and sever neonatal jaundice
with increased neurotoxic effects of
unconjugated bilirubin.
Intracranial hemorrhage.
Necrotizing enterocolitis.
Prediction Screening for
PTL
1.PAST OBSTETRIC HISTORY

If woman has a single previous


PTL increases the risk of PTL
4times when compared with
–ve such history.
2. BACTERIAL VAGINOSIS
• Is abnormality of normal vaginal flora
characterized by a reduced numbers of
lactobacilli, higher PH& increased
numbers of potential pathogens:-
Gardenerella vaginalis ,bacteriodes
,Eschersia coli .
• There is double risk of preterm delivery
3. ULTRASOUND MEASUREMENT OF CERVICAL LENGTH

Normal cervix measures about 35 mm Either


serial measuring of cervical length in 2nd
&early 3rd trimester.
Or single measurement of cervical length at
18 -22 w.
At any gestational age there is relationship
between cervical length &the risk of PTL
4.Fetal fibronectin (FFN) testing.
Fetal fibronectin
(fFN) is glue-like protein binding the choriodecidual
membranes . Rarely seen in the cervico-vaginal
secretion between 23-34 weeks . release of fFN
indicate disruption of the choriodecidual interface
which can be caused by preterm labor ,infection ,
stress ,or hemorrhage .
PREVENTION OF PRETERM DELIVERY:

1-Life style modification coupled with optimal


management can reduce the incidence of
preterm delivery (stop smoking , adequate
nutrition).
2-Cervical cerculage : prophylactic cerculage
in asymptomatic patient with short cervix
diagnosed by ultrasound or patient with
history suggestive of cervical
incompetence.
3-Progesterone: progesterone has many
cellular functions which maintain
pregnancy and it’s withdrawal is a
prerequisite for labor.
4-non-steroidal anti-inflamatory drugs
NSAIDs may be beneficial

5-Screening and treatment of bacterial


vaginosis early in pregnant who are high
risk.
MANAGEMENT OF PRETERM LABOR:

History :
- proper estimation of the gestational age with the regard of
the previous ultrasonic assessment to confirm that the
baby is preterm.
-symptoms of PTL/PROM:
-Abdominal pain : not necessarily regular .
-Backache.
-Leaking liquor .
-Vaginal discharge/Vaginal bleeding.
- Underlying condition predispose to PTL:
medical (UTI ,gastroenteritis), obstetric (APH , previous
PTL) or fetal (anomaly ,death).
Examination :
General : to exclude maternal disease as systemic
infection , dehydration ,hypertension.
Abdominal examination:
-exclude underlying abdominal pathology as
appendicitis, pyelonephritis .
-obstetric examination : palpable uterine contraction,
fundal height , lie , presentation , fetal heart.
Pelvic examination : to exclude cervical dilatation and
effacement, rupture of the membrane, infection
,bleeding.
INVESTIGATION :

• GUE (mid stream)


• High Vaginal Smear.
• blood culture is indicated if pyrexia more
than 38.5.
• C-reactive protein and ESR in cases of
rupture of membrane.
• Abdominal ultrasound.
TREATMENT:

Initial treatment :
- Bed rest in lateral decubitus.
- external cardiotocographic monitoring .
- tocolysis.
- steroid administration.
TOCOLYTIC DRUGS
1. Beta- adrenergic agonists.
Ritodrine,salbutamol,turbutaline.
2. Mg sulphate .
3. NSAIDs. Indomethacin,
4. Ca channel blockers. Nifidipine.
5. Glyceryl trinitrate. Nitroglycerine patch.
6. Oxytocin antagonists. Atosiban.
2.ANTENATAL CORTICOSTEROID:

Betamethasone and dexamethasone 24 mg


divided in 2-4 doses
improve neonatal outcome by reducing
respiratory distress syndrome , intraventricular
hemorrhage , necrotizing
enterocolitis.
Management of preterm delivery :
If labour become established certain point are differs
from delivery of term pregnancy:
Continuous CTG monitoring (more risk of fetal distress ).
Delivery of the fetus in their sac is better or to delay
rupture of the membrane as late as possible in labour
to protect the fragile fetus from birth trauma.
caesarean section indicated in preterm breech presentation
,preterm twin or higher order multiple pregnancy .
classical C.S. may be indicated in extreme prematurity.
Assisted delivery to shorten the second stage of labour
by forceps not ventouse to reduce the risk of I.C.trauma.

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