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Year : 2016 Month : June Volume : 5 Issue : 51 Page : 3245-3247

PERINATAL AND MATERNAL OUTCOME IN PREMATURE RUPTURE OF MEMBRANES.

Mercy Rodrigo Rexy Rodrigo1, Abiramavalli Kannamani2

1Senior Assistant Professor, Department of Obstetrics and Gynaecology, Thoothukudi Medical College.
2Senior Assistant Professor, Department of Obstetrics and Gynaecology, Institute of Obstetrics and Gynaecology, Egmore, Chennai.

CORRESPONDING AUTHOR

Dr. Mercy Rodrigo Rexy Rodrigo,
Email : mercyravi2003@gmail.com

ABSTRACT

Corresponding Author:
Dr. Mercy Rodrigo Rexy Rodrigo,
102-B, Kaliappar Street,
Thoothukudi-1.
E-mail: mercyravi2003@gmail.com

ABSTRACT

BACKGROUND

The objectives of this study are 1) To find out the incidence of premature rupture of membranes, 2) To evaluate the aetiology of premature rupture of membranes, 3) To assess foetal and maternal outcome in premature rupture of membranes.

MATERIAL AND METHODS

This prospective case control study was conducted in Govt. RSRM Lying In Hospital, Chennai, over a period of 6 months and 100 cases of spontaneous rupture of membranes attending the Department of Obstetrics and Gynaecology were studied. Maternal and neonatal outcome were compared with controls.

 

RESULTS

Incidence of PROM was 9.06%. Most of them belonged to low socioeconomic class and in the age group 20-29 years, commonly seen primi gravida and in unbooked cases. Aetiological analysis revealed infection in 15% of cases, which is evident by positive amniotic fluid culture, h/o recent coitus in 20%, mal-presentation in 7%. Cause is unknown in most of the cases. The caesarean section rate is 24% when compared to 12% in control group. The PROM group had higher morbidities like postpartum haemorrhage, postpartum fever, wound infection, neonatal sepsis.

CONCLUSION

This study showed significantly increased morbidity for both mother and baby. PROM causes major increase in the incidence of prematurity, hence careful screening of high risk factors and treatment of infection promptly is needed to decrease the perinatal morbidity and mortality.

KEYWORDS

PROM, LSCS, Maternal Morbidity, Neonatal Morbidity.

INTRODUCTION

Rupture of membranes before the onset of labour is defined as premature rupture of membranes. If it occurs before 37 weeks, it is called preterm PROM. If it occurs after 37 weeks, it is called as term PROM.[1] It complicates 5-10% of term pregnancies, about 30% of preterm deliveries.[2] 80% of PROM cases gets into labour spontaneously within 24 hours and the remaining within 72 hours.

In term PROM, if Bishop’s score is favourable immediate stimulation policy is associated with good foetal and maternal outcome. If not, induction with prostaglandins is recommended.[3,4,5] Problems for the mother includes chorioamnionitis, postpartum fever, wound infection. Major problem for the baby includes infection, prematurity, non-reassuring foetal heart rate pattern due to cord compression.[6]

MATERIALS AND METHODS

For this prospective study, 100 cases of pregnant women with PROM is taken as study group and equal number of cases with no PROM and no complication are taken as controls.

Inclusion Criteria

  1. Singleton pregnancy between 28-42 weeks of gestation.
  2. Primi and multi gravida.
  3. Age group 18-40 years.
  4. Leaking from cervix confirmed by speculum examination.
  5. Cervix dilatation less than 3 cms.
  6. No uterine contractions.

 

Exclusion Criteria

  1. Multiple pregnancies.
  2. Maternal complications interfering with active management of PROM like PIH, heart disease, previous LSCS.

 

Study group was further classified into term PROM and preterm PROM. All the patients were admitted in labour ward and started on 1 gm of Ampicillin every 6 hours and managed individually. Amniotic fluid culture and sensitivity was sent for all cases with PROM. Progress of labour was carefully monitored. Depending upon the maternal and foetal condition, labour was terminated by vaginal/instrumental/operative methods. For cases less than 34 weeks, corticosteroids were given. After delivery maternal and foetal outcome were studied. Foetal morbidity cases were admitted in NICU and subjected to investigations and followed till discharge. Mothers are also followed till discharge.

RESULTS

Incidence in Govt. RSRM Lying–in Hospital 9.06%.

Age in Years

Study

Control

<20

9

9

20-29

85

85

30-40

6

6

TOTAL

100

100

Table 1: Age Incidence in PROM

 

 

SE Class

Study

Control

Low (IV & V)

98

97

Middle (III)

2

3

Total

100

100

Table 2: Socio-Economic Status in PROM

 

An. Booking

Study

Control

Booked

38

60

Unbooked

62

40

Total

100

100

Table 3: Antenatal Care & PROM

 

P<0.001 - significant

 

Parity

Study

Control

G1

67

68

G2

17

18

G3

13

11

G4

3

3

Table 4: Parity Incidence in PROM

 

Gestation in WKS

Study

Control

<34

3

-

34-36

17

2

>37

80

98

Total

100

100

Table 5: Incidence of PROM in

 Relation to Gestational Age

 

 

Cause

No. of Positive Cases

Infection

15

H/O coitus

20

Mal-presentation

7

H/O cervical surgery

1

Not known

57

Total

100

Table 6: Aetiological Analysis in PROM

 

Organisms Grown

No. of Cases

%

E. Coli

6

40

Streptococci

2

13.33

Klebsiella

4

26.66

Proteus

2

13.33

Pseudomonas Aeruginosa

1

6.66

Total

15

100

Table 7: Bacteriological Study of

Amniotic Fluid in PROM

 

 

 

PROM

Mode of Onset of Labour

Spontaneous

Induction

Term

26

54

Preterm

14

6

Table 8: Mode of Onset of Labour and PROM

PROM

Latent Period

<24 Hours

>24 Hours

Term

77

3

Pre-Term

13

7

Table 9: Relation of Latent Period and PROM

 

 

Mode of Delivery

Study

Control

Term

Pre-Term

Vaginal Delivery

58

15

86

LSCS

19

5

12

LMC

2

-

-

Assisted Breech Delivery

1

-

2

Total

80

20

100

Table 10: Mode of Delivery and PROM

 

 

Gestation

No. of Cases

LSCS

%

Pre-Term

20

5

25%

Term

80

19

23.75%

Table 11: Caesarean Section in Term PROM and PPROM

 

WT. of Baby in KG

Study

Control

<2 KG

6

-

2-2.5 KG

51

6

>2.5 KG

43

94

Total

100

100

Table 12: Baby Birth Weight in PROM

 

 

5’ Apgar Score

Study

Control

2/10

1

-

6/10

1

-

7/10

10

5

8/10

71

66

9/10

17

29

TOTAL

100

100

Table 13: 5’ Apgar Score in PROM

 

Morbidity

No. of Cases

Term

Pre-Term

PPH

3

 

Clinical Chorioamnionitis

_

_

Postpartum Fever

1

1

Wound Infection

7

 

Table 14: Maternal Morbidity in PROM

 

Morbidity

Preterm

Term

No. of Cases

%

No. of Cases

%

Sepsis

1

2.7

4

11.11

RDS

6

16.66

4

11.11

Birth Asphyxia

_

 

4

11.11

Prematurity/SGA

11

30.55

5

13.88

Meningitis

 

 

1

2.7

Total

18

50%

18

50%

Table 15: Perinatal Morbidity in

Term and Preterm PROM

 

Maturity

No. of Cases

%

Term

1

1.25

Preterm

2

10

Table 16: Perinatal Mortality in PROM

                                        

Causes

Study

No. of Cases

%

Prematurity

2

66.66%

Birth Asphyxia/RDS

1

33.33%

Table 17: Causes of PN Mortality in PROM

 

DISCUSSION

The incidence of PROM was 9.06% in this study, reported mainly in unbooked cases and women of low socioeconomic group. This is almost similar to the incidence of PROM in study conducted by Alberto Bacchi Madena et al (9-10%).[7] Arias (7-20%).[8] Distribution of cases with regard to parity was not significant in this study (Table IV). The cause is idiopathic in most of the cases. Recent coitus, infection, mal-presentation were some of the risk factors identified in this study. This study also showed shorter the gestation longer will be the latency period and vice versa (Table IX).

In this study normal delivery is the commonest mode of delivery and the result is 76%, which is similar to V. Kamala et al study.[9] LSCS rate in study group is 24%, which is similar to Sita Ram Shreshta et al study.[10] LSCS was mainly done for mal-presentation and foetal distress. LSCS rate in preterm PROM is 25%, which is higher than term PROM mainly due to cervical dystocia and foetal distress.

The most dreaded complication of PROM is chorioamnionitis.[11] But clinical evidence of infection is not seen in any of the cases due to intrapartum use of antibiotics. But 15% of patients in study group showed positivity in amniotic fluid culture (Table VI and VII). Only 2 patients had fever and 7 had wound infection. Among 3 cases of perinatal mortality, 2 babies died due to prematurity and its complications and one case due to birth asphyxia; 36 cases of perinatal morbidity was noted in study group, whereas only 4 cases had morbidities in control group. Even though PPROM is only 20% in this study, it contributes 50% to perinatal morbidity (Table XV).

SUMMARY

  • Management of PROM lies between immediate stimulation of labour and expectant line of management.
  • Immediate stimulation policy appears to be reasonable approach in multiparae and nulliparae with a good cervical score in term PROM.
  • Expectant line of management is beneficial for preterm PROM patients, but signs of infection warrant broad-spectrum antibiotics and prompt delivery.
  • Abnormal labour and operative procedures have increased in PROM.
  • This study showed careful antenatal monitoring for risk factors and aetiology detection and prompt treatment of infection and pelvic examination under aseptic precautions and appropriate antibiotics are important in prevention of PROM.

CONCLUSION

PROM is a high risk obstetric condition and it presents a great challenge to both obstetricians and paediatricians. Prompt diagnosis and effective management with careful selection of labour inducing agents are essential to deliver a healthy baby from a healthy mother.

REFERENCES

  1. Onnig Tamizian, Arul kumaran S. Prelabour rupture of membranes. In: Arulkumaran S, Penna LK, Rao KB, editors. The management of labour Chennai: Orient longman publisher 2005;2nd ed:306-317.
  2. Royal college of obstetrician-gynaecologists (RCOG), scientific advisory committee. Preterm prelabour rupture of membranes. Clinical green top guidelines No.44 London, UK: RCOG 2006;381391. Available at:http//www.rcog.org.uk/resources/public/pdf/green_top44_preterm.pdf.
  3. Hidar S, Bibi M, Jerbi M, et al. Contribution of intra cervical PGE2 administration in PROM at term prospective randomized clinical trials. Journal Obs & Gynaec Bioreproduction 2000;29(6):607-13.
  4. Wagnar MV, Chin VP, Peters CJ, et al. A Comparison of early and delayed induction of labour with spontaneous rupture of membranes at term. Obstetrics and Gynaecology of India 1989;74(1):93-7.
  5. Ozden S. Intravaginal misoprostol versus expectant management in prom with low Bishop’s score at term. IJOG 2002;77(2):109-15.
  6. Merowits NB, Anthony CV, Smulian JC, et al. Effect of labour on infant morbidity and mortality with prom: United States population- based study. Obstetrics and Gynaecology 2001;97(4):494-8.
  7. Modena AB, Kaihura C, Fieni S. Pre labour rupture of membranes: recent evidence. Acta Biomed 2004;75(1):5-10.
  8. Arias F, Daftary SN, Bhide AG. Premature rupture of membranes: in: practical guide to high risk pregnancy and delivery. Elsevier health sciences 2008;3rd ed.
  9. Kamala Jeyaram V, Scaila Sudha. A study of premature rupture of membranes- management and outcome. Journal of Obstetrics and Gynaecology of India 2001;51(2):58-60.
  10. Sita Ram Shrestha, Paban Sharma. Foetal outcome of pre-labour rupture of membranes. N J Obstet Gynaecol 2006;1(2):19-24.
  11. Amira El-Messidi, Alan Cameron. Diagnosis of premature rupture of membranes: inspiration from past and insights for future. JOGC 2010;32(6):561-69.

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