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Prem
atureLabor
OR
Pretermlabour
DrBakhtawar
Prematurelabour
(Pretermlabour)
INTRODUCTION
➢Premature labour is generally a labour
that occurs after 20 wks & before
37 completed wks of gestation
DEFINITION
Preterm labour
(PTL) is defined
as one where the
labour starts
before the 37th
completed week
(<259 days),
counting from the
1stday of the last
menstrual period
DEFINITION
●Pre term labour is defined by WHO
as onset of labour prior to the
completion of 37 weeks of gestation
in a pregnancy beyond 20 weeks of
gestation.
INCIDENCE
Approx. 10% of deliveries in public
hospital occur before the 37t
h week
A much smaller %age is involved in
the 24-32 weeks period.
The prevalence widely varies and
ranges between 5-10%
ETIOLOGY
In about 50%, the cause of preterm
labour is not known
But some of the high risk factors are:
HISTORY
COMPLICATIONS
In Present
Pregnancies
IATROGENIC
IDIOPATHIC
Conti..
HISTORY-
-previous history of abortion or
preterm delivery
-recurrent UTI
-smoking habits
-low socio-economic & nutritional status
Malpresentations Previous abortion history
Conti..
COMPLICATIONS IN PRESENT
PREGNANCY- It may be due to 3
causes:-MATERNAL
-FETAL
-PLACENTAL
A) MATERNAL :
Pregnancy
Uterine anomalies
Genital tract
infection
Medical & surgical
illness
INFECTION PRE ECLAMPSIA
Incompetent cervix malformation of uterus
Conti..
FETAL : - Multiple pregnancy
- Congenital malformations
- IUD
PLACENTAL :- Infarction
-Thrombosis
- Placenta praevia or
abruption
Conti..
IATROGENIC:
-Elective induction with wrong
estimation of gestational period.
- IDIOPATHIC:
-Premature effacement of cervix with
hyper-irritable uterus
-Early engagement of head
ETIOPATHOGENESIS
ACTIVATION OF FETAL HPA AXIS
CRH, Cortisol PGE2, F2α
TXA2,
Leukotrienes
↓PG Dehydrogenase
proteases
choriodecidual bacterial
Colonisation TNF,
IL-1,6,8
myometrial
PATHOLOGIC UTERINE ENLARGEMENT contraction
(Polyhydramnios , multiple pregnancy) cervical
Mechanical stretch, IL8 ripening
Gap junction, PG Synthesis
preterm labour and
delievery
Chorion, amnion
&
decidua
Risk factors
❖Low BMI
❖Short maternal height
❖History of spontaneous pre term birth
❖Bacterial vaginitis.
❖Asymptomatic bacteriuria
❖Low socio economic status
❖Short cervical length
Factors influencing during
pregnancy
❑Multiple pregnancy
❑Use of fertility medication
❑High blood pressure
❑Pre –eclampsia
❑Maternal diabetes mellitus
❑Asthma
❑Thyroid disease
Cont..
❑Heart diseases
❑Uterine malformations
❑Placenta praevia
❑Abruptio placenta
❑Poly hyrdaminos
❑Oligohydramnios
❑Anxiety & depression
❑Use of tobacco, cocaine
❑Excessive alcohol during pregnancy
❑ babies with birth defects
SIGN AND SYMPTOMS
❖Backache
❖Contractions every 10 minutes are more
often
❖Cramping in lower abdomen
❖Menstrual like cramps( feel like gas pain ,
not a/w diarrhea)
❖Fluid leaking from vagina
❖Flu like symptoms- nausea, vomiting,
diarrhea
Cont..
●Increased pressure in pelvis
●Increased vaginal bleeding
●Regular uterine activity
●Vaginal spotting
●Pelvic pressure
DIAGNOSIS
❖ Regular uterine contractions with or without
pain (at least one in every 10 mins.)
❖ Dilatation(≥2cm) & Effacement (80%) of the
cervix
Length of cervix ≤2.5cm
Funnelling of internal OS
❖
❖
❖ Pelvic pressure, backache or vaginal
discharge or bleding.
INVESTIGATIONS
●Full blood count
●Routine urine-analysis,culture &
senstivity
●Cervicovaginal Swab-
culture,FIBRONECTIN
●Serum electrolytes & glucose levels
when tocolytic agents are to be
used
● USG-fetal well being,
cervical length &
placental
localization
FIBRONECTIN
➢A PROTEIN that binds
the FETAL MEMBRANES
to DECIDUA
➢Normally found in
CERVICOVAGINAL
discharge before 22wks &
again after 37wks of
pregnancy
PRESENCE OF
FIBRONECTIN IN CVD
B/W 24Wks & 34 Wks
PREDICTS PRE-TERM
LABOUR
MANAGEMENT
●It includes
Arrest of preterm
Labour, if not
contraindicated
Appropriate management
Prevention,if possible
Neonatal care
Prevention of Preterm
Labour
Primary Care –
to reduce the incidence of preterm
labour by reducing the high risk factors (e.g.
infection etc.)
Secondary Care
includes screening tests for early detection
& prophylactic treatment (e.g. tocolytics)
Tertiary care-
to reduce the perinatal morbidity &
mortality after the diagnosis (e.g. use of
corticosteroids)
Cont..
●Seek regular prenatal care
●Eat a healthy diet
●Gain weight wisely
●Avoid risky substances
●Consider pregnancy spacing
●Be cautious when using assisted
reproductive technology (ART)
●Taking preventive medications , who has
short cervix( Progesterone)
●Restricting sexual activity.
●Limiting certain physical activities.
●Managing chronic conditions such as DM,
Increased BP.
ARRESTING PRETERM
LABOU R
●BED REST-Left lateral position
●ADEQUATE HYDRATION
●PROPHYLACTIC ANTIBIOTIC
●TOCOLYTIC AGENTS-Eg.TERBUTALINE
INDOMETHACIN
NIFEDIPINEs
short term long term
Conti..
●SHORT TERM THERAPY
Most successful therapy
OBJECTIVES:
-TO DELAY delivery for 48hrs for
glucocorticoid therapy to mother to
enhance
enhance fetal lung maturation
-IN UTERO TRANSFER of the patient to a
unit more able to manage a preterm neonate
GLUCOCORTICOID
THERAPY
●Advocated in pregnancy less than 34
wks.
●Helps in fetal lung maturation
●Reduces incidence of RDS & IVH
RISKS
●PROM with evidence of infection
●IDDM where patients needs insulin dose
readjustment
Conti..
CONTRA-INDICATIONS
MATERNAL FETAL OTHERS
❑Gestational
diabetes
❑Placenta praviea.
❑In case of
placental
abnormalities.
APPROPRIATE
MANAGEMENT
There are basically 2 principles:
To prevent birth asphyxia & development
of RDS
To prevent birth trauma
FIRST STAGE
❑Patient is put to bed to prevent PROM
❑To ensure adequate fetal oxygenation
❑Strong sedative avoided
❑Epidural analgesia is of choice
❑Labour should be watched by intensive
clinical monitoring
❑In case of delay, caesarean section
should be performed
SECOND STAGE
❖ The birth should be gentle & slow to avoid rapid
compression & decompression of head
❖ Episiotomy may be done under local anesthesia to
minimize head compression if there is perineal
resistance
❖ Tendency to delay is curtailed by low forceps. Routine
forceps is not indicated
❖ The cord is to be clamped immediately at birth to
prevent HYPERVOLEMIA & HYPERBILIRUBINEMIA
❖ To shift the baby to intensive neonatal care unit
under care of NEONATOLOGIST
IMMEDIATE
MANAGEMENT
● The cord is to be clamped quickly
● The cord length is kept long in case exchange
transfusion is required
● The air passage should be cleared of mucus
● Adequate oxygenation
● Aqueous solution of vit.k 1mg given I/M to
prevent hemorrhagic manifestations
● The baby should be wrapped including head in
a sterile warm towel
NURSING MANAGEMENT
1. Assess the mother’s condition to evaluate
signs of labour.
❑ Obtain a through obstetrics history
❑ Determine the frequency , duration,&
intensity of uterine contraction.
❑ Determine the cervical dilatation and
effacement.
❑ Assess the status of membranes, and
bloody show
Cont..
2.Evaluate the factors for distress, size and
maturity.
(sonography & lecithin-sphingomyelin ratio)
3.Perform measures to manage or stop pre
term labour.
●Place the client on bed rest in the side
lying position.
●Prepare for possible ultrasongraphy,
amniocentesis, tocolytic drug therapy or
steroid therapy.
●Administer tocoltyic agent as prescribed.
Assess for side effects of tocolytic therapy
❖Decreased maternal Blood pressure
❖Dyspnea
❖Chest pain
❖FHS >180beats/min
Cont..
●4- provide physical and emotional support
●5- Provide adequate hydration
●6- Provide client and family education.
PROGNOSIS
●Results in high
-perinatal mortality
-perinatal morbidity
• With intensive neonatal care unit,
survival rate of the baby weighing b/w
1000 to 1500 gm is more than 90%
• WITH USE OF SURFACTANT, survival
rate of infants born at 26wks is about
80%
EDUCATIO
N
❑All PREGNANT women
should recognize
following S/S ‘s:-
-uterine contractions
every 10-15 minutes or
less
-menstrual-like cramping
-dull backache
-lower abdominal
pressure
-diarrhea
-increase or change in
vaginal discharge
-vaginal bleeding
Premature Labor Signs, Causes and Management

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Premature Labor Signs, Causes and Management

  • 3. INTRODUCTION ➢Premature labour is generally a labour that occurs after 20 wks & before 37 completed wks of gestation
  • 4. DEFINITION Preterm labour (PTL) is defined as one where the labour starts before the 37th completed week (<259 days), counting from the 1stday of the last menstrual period
  • 5. DEFINITION ●Pre term labour is defined by WHO as onset of labour prior to the completion of 37 weeks of gestation in a pregnancy beyond 20 weeks of gestation.
  • 6. INCIDENCE Approx. 10% of deliveries in public hospital occur before the 37t h week A much smaller %age is involved in the 24-32 weeks period. The prevalence widely varies and ranges between 5-10%
  • 7. ETIOLOGY In about 50%, the cause of preterm labour is not known But some of the high risk factors are: HISTORY COMPLICATIONS In Present Pregnancies IATROGENIC IDIOPATHIC
  • 8. Conti.. HISTORY- -previous history of abortion or preterm delivery -recurrent UTI -smoking habits -low socio-economic & nutritional status
  • 10. Conti.. COMPLICATIONS IN PRESENT PREGNANCY- It may be due to 3 causes:-MATERNAL -FETAL -PLACENTAL A) MATERNAL : Pregnancy Uterine anomalies Genital tract infection Medical & surgical illness
  • 13.
  • 14. Conti.. FETAL : - Multiple pregnancy - Congenital malformations - IUD PLACENTAL :- Infarction -Thrombosis - Placenta praevia or abruption
  • 15.
  • 16. Conti.. IATROGENIC: -Elective induction with wrong estimation of gestational period. - IDIOPATHIC: -Premature effacement of cervix with hyper-irritable uterus -Early engagement of head
  • 17. ETIOPATHOGENESIS ACTIVATION OF FETAL HPA AXIS CRH, Cortisol PGE2, F2α TXA2, Leukotrienes ↓PG Dehydrogenase proteases choriodecidual bacterial Colonisation TNF, IL-1,6,8 myometrial PATHOLOGIC UTERINE ENLARGEMENT contraction (Polyhydramnios , multiple pregnancy) cervical Mechanical stretch, IL8 ripening Gap junction, PG Synthesis preterm labour and delievery Chorion, amnion & decidua
  • 18. Risk factors ❖Low BMI ❖Short maternal height ❖History of spontaneous pre term birth ❖Bacterial vaginitis. ❖Asymptomatic bacteriuria ❖Low socio economic status ❖Short cervical length
  • 19. Factors influencing during pregnancy ❑Multiple pregnancy ❑Use of fertility medication ❑High blood pressure ❑Pre –eclampsia ❑Maternal diabetes mellitus ❑Asthma ❑Thyroid disease
  • 20. Cont.. ❑Heart diseases ❑Uterine malformations ❑Placenta praevia ❑Abruptio placenta ❑Poly hyrdaminos ❑Oligohydramnios ❑Anxiety & depression ❑Use of tobacco, cocaine
  • 21. ❑Excessive alcohol during pregnancy ❑ babies with birth defects
  • 22. SIGN AND SYMPTOMS ❖Backache ❖Contractions every 10 minutes are more often ❖Cramping in lower abdomen ❖Menstrual like cramps( feel like gas pain , not a/w diarrhea) ❖Fluid leaking from vagina ❖Flu like symptoms- nausea, vomiting, diarrhea
  • 23. Cont.. ●Increased pressure in pelvis ●Increased vaginal bleeding ●Regular uterine activity ●Vaginal spotting ●Pelvic pressure
  • 24. DIAGNOSIS ❖ Regular uterine contractions with or without pain (at least one in every 10 mins.) ❖ Dilatation(≥2cm) & Effacement (80%) of the cervix Length of cervix ≤2.5cm Funnelling of internal OS ❖ ❖ ❖ Pelvic pressure, backache or vaginal discharge or bleding.
  • 25. INVESTIGATIONS ●Full blood count ●Routine urine-analysis,culture & senstivity ●Cervicovaginal Swab- culture,FIBRONECTIN ●Serum electrolytes & glucose levels when tocolytic agents are to be used
  • 26. ● USG-fetal well being, cervical length & placental localization
  • 27. FIBRONECTIN ➢A PROTEIN that binds the FETAL MEMBRANES to DECIDUA ➢Normally found in CERVICOVAGINAL discharge before 22wks & again after 37wks of pregnancy PRESENCE OF FIBRONECTIN IN CVD B/W 24Wks & 34 Wks PREDICTS PRE-TERM LABOUR
  • 28.
  • 29. MANAGEMENT ●It includes Arrest of preterm Labour, if not contraindicated Appropriate management Prevention,if possible Neonatal care
  • 30. Prevention of Preterm Labour Primary Care – to reduce the incidence of preterm labour by reducing the high risk factors (e.g. infection etc.) Secondary Care includes screening tests for early detection & prophylactic treatment (e.g. tocolytics) Tertiary care- to reduce the perinatal morbidity & mortality after the diagnosis (e.g. use of corticosteroids)
  • 31. Cont.. ●Seek regular prenatal care ●Eat a healthy diet ●Gain weight wisely ●Avoid risky substances ●Consider pregnancy spacing ●Be cautious when using assisted reproductive technology (ART)
  • 32. ●Taking preventive medications , who has short cervix( Progesterone) ●Restricting sexual activity. ●Limiting certain physical activities. ●Managing chronic conditions such as DM, Increased BP.
  • 33. ARRESTING PRETERM LABOU R ●BED REST-Left lateral position ●ADEQUATE HYDRATION ●PROPHYLACTIC ANTIBIOTIC ●TOCOLYTIC AGENTS-Eg.TERBUTALINE INDOMETHACIN NIFEDIPINEs short term long term
  • 34. Conti.. ●SHORT TERM THERAPY Most successful therapy OBJECTIVES: -TO DELAY delivery for 48hrs for glucocorticoid therapy to mother to enhance enhance fetal lung maturation -IN UTERO TRANSFER of the patient to a unit more able to manage a preterm neonate
  • 35. GLUCOCORTICOID THERAPY ●Advocated in pregnancy less than 34 wks. ●Helps in fetal lung maturation ●Reduces incidence of RDS & IVH RISKS ●PROM with evidence of infection ●IDDM where patients needs insulin dose readjustment
  • 38. APPROPRIATE MANAGEMENT There are basically 2 principles: To prevent birth asphyxia & development of RDS To prevent birth trauma
  • 39. FIRST STAGE ❑Patient is put to bed to prevent PROM ❑To ensure adequate fetal oxygenation ❑Strong sedative avoided ❑Epidural analgesia is of choice ❑Labour should be watched by intensive clinical monitoring ❑In case of delay, caesarean section should be performed
  • 40. SECOND STAGE ❖ The birth should be gentle & slow to avoid rapid compression & decompression of head ❖ Episiotomy may be done under local anesthesia to minimize head compression if there is perineal resistance ❖ Tendency to delay is curtailed by low forceps. Routine forceps is not indicated ❖ The cord is to be clamped immediately at birth to prevent HYPERVOLEMIA & HYPERBILIRUBINEMIA ❖ To shift the baby to intensive neonatal care unit under care of NEONATOLOGIST
  • 41. IMMEDIATE MANAGEMENT ● The cord is to be clamped quickly ● The cord length is kept long in case exchange transfusion is required ● The air passage should be cleared of mucus ● Adequate oxygenation ● Aqueous solution of vit.k 1mg given I/M to prevent hemorrhagic manifestations ● The baby should be wrapped including head in a sterile warm towel
  • 42. NURSING MANAGEMENT 1. Assess the mother’s condition to evaluate signs of labour. ❑ Obtain a through obstetrics history ❑ Determine the frequency , duration,& intensity of uterine contraction. ❑ Determine the cervical dilatation and effacement. ❑ Assess the status of membranes, and bloody show
  • 43. Cont.. 2.Evaluate the factors for distress, size and maturity. (sonography & lecithin-sphingomyelin ratio) 3.Perform measures to manage or stop pre term labour. ●Place the client on bed rest in the side lying position. ●Prepare for possible ultrasongraphy, amniocentesis, tocolytic drug therapy or steroid therapy.
  • 44. ●Administer tocoltyic agent as prescribed. Assess for side effects of tocolytic therapy ❖Decreased maternal Blood pressure ❖Dyspnea ❖Chest pain ❖FHS >180beats/min
  • 45. Cont.. ●4- provide physical and emotional support ●5- Provide adequate hydration ●6- Provide client and family education.
  • 46. PROGNOSIS ●Results in high -perinatal mortality -perinatal morbidity • With intensive neonatal care unit, survival rate of the baby weighing b/w 1000 to 1500 gm is more than 90% • WITH USE OF SURFACTANT, survival rate of infants born at 26wks is about 80%
  • 47. EDUCATIO N ❑All PREGNANT women should recognize following S/S ‘s:- -uterine contractions every 10-15 minutes or less -menstrual-like cramping -dull backache -lower abdominal pressure -diarrhea -increase or change in vaginal discharge -vaginal bleeding