The Incidence and Management Outcome of Preterm Premature Rupture of Membranes (PPROM) in a Tertiary Hospital in Nigeria
Okeke TC1,, Enwereji JO1, Okoro OS1, Adiri CO1, Ezugwu EC1, Agu PU1
1Department of Obstetrics and Gynaecology, University of Nigeria Teaching Hospital (UNTH), Enugu, Nigeria
Abstract
Preterm premature rupture of membranes (PPROM) complicates 3-8 percent of pregnancies and leads to one third of preterm deliveries. It results in increased risk of prematurity and leads to perinatal and neonatal complications with risk of fetal death. This article aims to determine the incidence and management outcome of PPROM in Enugu, Nigeria over a ten year period. This was a retrospective review of management outcome of PPROM at the UNTH Enugu from January 1st 1999 to December 31st, 2008. The frequency of 3.3% for PPROM and 7% perinatal death were recorded over the period. Preterm PROM is a major complication of pregnancies. Currently, there is no effective way of preventing spontaneous rupture of fetal membranes due to ignorance of its aetiology, with consequent inability to control its incidence. However, it is important that women be well informed regarding maternal, fetal and neonatal complications regardless of controversies of its management.
Keywords: incidence, management outcome, preterm premature rupture of membrane (PPROM), Enugu, Nigeria
American Journal of Clinical Medicine Research, 2014 2 (1),
pp 14-17.
DOI: 10.12691/ajcmr-2-1-4
Received November 22, 2013; Revised January 15, 2014; Accepted January 16, 2014
Copyright © 2013 Science and Education Publishing. All Rights Reserved.Cite this article:
- TC, Okeke, et al. "The Incidence and Management Outcome of Preterm Premature Rupture of Membranes (PPROM) in a Tertiary Hospital in Nigeria." American Journal of Clinical Medicine Research 2.1 (2014): 14-17.
- TC, O. , JO, E. , OS, O. , CO, A. , EC, E. , & PU, A. (2014). The Incidence and Management Outcome of Preterm Premature Rupture of Membranes (PPROM) in a Tertiary Hospital in Nigeria. American Journal of Clinical Medicine Research, 2(1), 14-17.
- TC, Okeke, Enwereji JO, Okoro OS, Adiri CO, Ezugwu EC, and Agu PU. "The Incidence and Management Outcome of Preterm Premature Rupture of Membranes (PPROM) in a Tertiary Hospital in Nigeria." American Journal of Clinical Medicine Research 2, no. 1 (2014): 14-17.
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1. Introduction
Preterm premature rupture of membranes (PPROM) is the spontaneous rupture of the fetal membranes during pregnancy before 37 weeks gestation in the absence of regular painful uterine contractions [1]. Premature rupture of membrane (PROM) is the rupture of the fetal membranes before the onset of labour. This spontaneous rupture of membrane is a normal component of labour and delivery [2]. Preterm PROM complicates 3-8% of pregnancies and leads to one third of preterm deliveries [3]. It increases the risk of prematurity and leads to other perinatal and neonatal complications with 1-2% risk of fetal death [4]. It can lead to significant fetal perinatal morbidity such as respiratory distress syndrome, neonatal sepsis, umbilical cord prolapse, placental abruptio and fetal death [5]. It can also lead to maternal morbidity such as postpartum endometritis, disseminated intravascular coagulopathy, maternal sepsis, delayed menses and Asherman syndrome. PPROM is an important cause of perinatal morbidity and mortality because it is associated with brief latency from membrane rupture to delivery, perinatal infection and umbilical cord compression due to oligohydramnios [6].
Numerous risk factors are associated with PPROM such as Black race, lower socioeconomic status, smokers, past history of sexually transmitted infections, previous preterm delivery, polyhydramnios and multiple pregnancy [5, 7]. Others are procedures such as cerclage and amniocentesis [5]. The aetiology is multifactorial [5, 6].
PPROM evaluation and management are important for improving neonatal outcomes. Accurate diagnosis of PPROM requires a thorough history, physical examination and ancilliary laboratory studies. These would allow for gestational age specific obstetric interventions to optimize perinatal outcome and reduce fetomaternal complications [5, 8]. Speculum examination to determine cervical dilatation is preferred because digital vaginal examination is associated with a decreased latency period and has potential for adverse sequelae [9]. The management of pregnancies complicated by PPROM is challenging, controversial and should be individualized. However, it should focus on confirming the diagnosis, validating gestational age, documenting fetal wellbeing and deciding on the mode of delivery which depends on gestational age, fetal presentation and cervical examination [2,12-20]. Current evidence suggests aggressive antibiotic therapy which is effective for increasing latency period and reducing infectious infant morbidity. Corticosteroids can reduce many neonatal complications particularly respiratory distress syndrome and intraventricular haemorrhage [5, 10, 13, 14, 15].
Expectant management or conservative management is best accomplished by in patient observation. It generally consists of initial prolonged continous fetal and maternal monitoring combined with modified bed rest to increase the opportunity for amniotic fluid re-accumulation and spontaneous membrane sealing. This approach is generally accepted and preferred because of the associated neonatal advantage and reduction in the risks of prematurity.
There is paucity of data on prevalence and management outcome of PPROMP in African Population including Nigeria, In order to address this problems, this study was designed to investigate the incidence and management outcome of PPROM in Enugu, Nigeria.
2. Methods
This was a 10-year retrospective study of PPROM at the University of Nigeria Teaching Hospital (UNTH) Enugu, Nigeria between January 1, 1999 and December 31, 2008. Data was retrieved from antenatal ward admission register, case files, theatre records and ward reports of 119 women who were treated for PROM over the study period. To be eligible for this study the following criteria were fulfilled: (1) the patient must have ruptured fetal membranes spontaneously and the gestational age must be below 37 completed weeks. (2) Labour must not start within 1 hour following spontaneous membrane rupture. (3) All cases of artificial rupture of fetal membranes are to be excluded from the study.
Medical records were reviewed by trained staff using pre-established and pilot data extraction forms. The records of women who had PROM during the study period were retrieved and data extracted. Information sort were socio-demographic characteristics (maternal age, parity, occupation, tribe and gestational age), birth weight, Apgar scores at 1st and 5th minutes, need for neonatal resuscitation and admission to new born special care unit (NBSCU), fetal outcome, maternal complications which could be reasonably be assumed to have resulted from PROM such as postpartum endometritis, disseminated intravascular coagulopathy, maternal sepsis and Asherman syndrome.
The data were analyzed by descriptive statistics using the statistical package for social science version 12 (SPSS Inc. Chicago, IL, USA) and the results expressed in descriptive statistics by simple percentages.
Approval for the study was obtained from the University of Nigeria Teaching Hospital Ethical Committee. The University of Nigeria Teaching Hospital was established in 1970 and one of the oldest tertiary care centre in Eastern Nigeria. It receives high risk obstetric cases from this region. The antenatal clinics are run every working day (Monday to Friday). Patients are seen at every 4 weeks till 28weeks, fortnightly till 36 weeks, and then, weekly till delivery. At booking, obstetric, medical, and surgical history is obtained. Gestational age was estimated from the first day of the last menstrual period and was collaborated with ultrasonography. The first trimester ultrasound if available at booking was preferred. Height, weight and blood pressure were also measured. The following routine investigations were also done, packed cell volume, urinalysis, blood group and rhesus factor, genotype, hepatitis B surface antigen, VDRL (Veneral Disease Research Laboratory), HIV screening and ultrasound assessment. Pelvic examination using a sterile speculum was performed. Digital examination was avoided. Diagnosis of PPROM was based on history and confirmed by the presence of pooled amniotic fluid on a sterile speculum, positive results from a ferning test and trans-vaginal ultrasonographic evaluation that demonstrated oligohydramnios. Each patient was observed in the labour and delivery room for at least 24 hours.
3. Results
During the study period, 2798 deliveries were recorded. There was 119 cases of premature rupture of fetal membranes, out of which 94 were cases of preterm premature rupture of membranes, while 25 were cases of term premature rupture of membranes. This showed an incidence of 4.2% for premature rupture of membranes in general and 3.3% for preterm premature rupture of membranes of all deliveries. The case notes of 10 patients could not be traced. While the case note of another 5 unbooked patients had scanty information documented in them and were removed from the analysis leaving a total of 79 patients out of the 94 that met the criteria for preterm premature rupture of membranes, for analysis and evaluation.
Table 1 compared the relationship of PPROM to maternal age. PPROM is highest among reproductive age group of 26-30 years but lowest among reproductive age group 16-20 and 41 year and above. Primigravidae had the highest occurrence of PPROM. Increasing parity does not significantly influence the incidence of PPROM as shown in Table 2. The incidence of PPROM is highest among maternal heights 161-165cm and 156-160cm but lowest among extremes of maternal heights as shown in Table 3. Table 4 shows the relationship of PPROM to maternal morbidity. A total of 16 cases (20%) had complications which led to prolonged hospital stay. 11 women out of the 16 patients were febrile and 7 women out of the 11 women that had febrile illness had secondary postpartum haemorrhage (PPH) and one out of this patients had total abdominal hysterectomy (TAH) because of uncontrollable secondary PPH haemorrhage. One patient had offensive lochia, one patient had puerperal psychosis as a result of neonatal death while one patient had puerperal depression, one patient had umbilical cord prolapse.
Table 5 shows the relationship of the GA at which PROM occurred, the latency period with birth weight and perinatal death. All the babies delivered before gestational age (GA) of 34 weeks weighed < 2.5kg while 20 babies delivered after 35-36 weeks weighed > 2.5kg while 17 babies delivered after 35-36weeks still weighed < 2.5kg. Four perinatal deaths occurred in those with gestational age between 26-30weeks and 3 perinatal deaths occurred in those with gestational age between 31-34 weeks. No perinatal death was recorded in those with gestational age between 35 weeks and above. 59.5% had preterm PROM in those with gestational age between 35-36weeks +6days while 32.9% had preterm PROM in those with gestational age between 31-34 weeks and less number of cases occurred in those remote from term.
4. Discussion
The incidence of preterm premature rupture of membranes of 3.3 percent in this study fell within the range of 3-8 percent reported in a review by Egarter et al [16]. However, this incidence is slightly higher than the 3 percent reported by Meis et al [17]. This difference could be explained by the fact that many patients in this review had latency period less than one hour and were therefore not included by definition in the current study.
Stuart et al [18] reported that the incidence of preterm PROM rose with advancing maternal age. However, this study was not in agreement with this observation. This current study showed a peak incidence at the mid-reproductive age group of 26-30years (43%). Also in this study, 67.1% was recorded in multigravida while 29.1% was recorded in primigravida.
Incidence of PPROM was high in women with short stature as was documented by Babson and Benson in their previous work [19]. However, this study did not show such association, since there was a high incidence of 87.3% in those more than 155 cm tall.
The risk of infection is significant following PPROM. In this study, infection was the most important complication of PPROM and similar observation was noted by Stuart and his colleagues [18]. Infection rate of 13.9 percent was noted in this study in the mothers both intrapartum and postpartum. In this study, there was increase in incidence of infection with increase latency period more than 24hours.
The rate of maternal morbidity of 20% reported in this study is high compared to previous study by Vermillion et al [20] but is an agreement with that reported by Yoon et al21. Previous studies by Egarter et al [16] and Davidson [22] reported that use of prophylactic antibiotic in PPROM reduces maternal morbidity. However, despite the fact that prophylactic antibiotic was used liberally in this study: maternal morbidity rate of 20% and perinatal mortality rate of 8.9% were reported. The lack of effectiveness of prophylactic antibiotic as noted in this study might be due to adultrated drugs in our environment and low socio-economic status of patients involved.
Harding et al demonstrated that use of corticosteroid in preterm PROM before 34 weeks gestation reduces perinatal morbidity and mortality by reducing the risk of respiratory distress syndrome, intraventricular hemorrhage and necrotizing enterocoditis [23]. In this study, steroid was used in all cases of PPROM below 34 weeks and this may be responsible for low incidence of respiratory distress syndrome, intraventricular haemorrhage and necrotizing enterocolitis observed in this study.
In the management of PPROM, the initial step is informed consent. Risks and benefits information must be given to the patient since she will participate in the management decision making. There are issues frequently observed in management of PPROM such as prematurity, infection morbidity and its complications. The principal risk to fetus is prematurity while the primary maternal risks are infection morbidity and its complications. In this study, the incidence of neonatal complications is high but comparable to that documented by Elimian et al [24] and Dexter et al [25]. This high neonatal complication may be related more closely to the effects of premature birth and sophistication of New born special care unit (NBSCU) rather than PROM.
Several areas of controversies exist regarding the best medical approach or management of PROM remote from term. Expectant management and immediate delivery are potential options in these patients, and each has its own merit and demerits. Expectant management are generally accepted and preferred since it is associated with neonatal advantage by reducing risks of prematurity.
Limitation of this study was the restriction of the study population to the UNTH, Enugu, Nigeria. The women who received care in other health institution outside UNTH and those who received no care at all were not included in this study. Furthermore, this small scale retrospective study should be interpreted with caution. However, this is a stepping stone towards further research on PPROM among Nigerian women.
PPROM is a major complication of pregnancies and an important cause of perinatal morbidity and mortality. Currently, there is no effective way of preventing spontaneous rupture of fetal membranes due to ignorance of its aetiology, with consequent inability to control its incidence. However, it is important that women be well informed regarding maternal, fetal and neonatal complications regardless of controversies of its management.
References
[1] | Fowlie A. Preterm pre-labour rupture of membranes, In:Arukumaran S, Symonds IM, Fowlie A (eds): Oxford Handbook of Obstetrics and Gynaecology. 2nd edition New Delhi, Oxford University Press 2004; 247-249. | ||
In article | |||
[2] | Caughey AB, Robinson JN, Norwitz ER. Contemporary Diagnosis and Management of Preterm Premature Rupture of Membranes. Rev. Obstet Gynecol 2008;1(1):11-22. | ||
In article | |||
[3] | Mercer BM, Goldenberg RL, Meis PJ, et al. The NICHD Maternal –Fetal Medicine Units Network, authors. The Preterm Prediction study: prediction of preterm premature rupture of membranes through clinical findings and ancilliary testing. Am J Obstet Gynecol 2000; 183: 738-745. | ||
In article | CrossRef | ||
[4] | Shucker JL, Mercer BM. Midtrimester PROM. Semin Perinatol 1996;20:389-400 | ||
In article | |||
[5] | Medina TM, Hill DA. Preterm Premature Rupture of Membranes: Diagnosis and management. Am Fam Physician 2006;73:659-664 | ||
In article | |||
[6] | Borna S, Borna H, Khazardoost S, Hantoushzadeh S. Perinatal outcome in preterm premature rupture of membranes with amniotic fluid index <5(AF1>5). BMC pregnancy and childbirth 2004; 4:15. | ||
In article | CrossRef | ||
[7] | Savitz DA, Blackmore CA. Thorp JM. Epidemiology characteristics of preterm delivery: etiology heterogeneity. Am J Obstet Gynecol 1991; 164: 467-471. | ||
In article | CrossRef | ||
[8] | Garite TJ. Management of Premature rupture of membranes. Clin Perinatol 2001; 28: 837-847. | ||
In article | CrossRef | ||
[9] | Alexander JM, Mercer BM, Miodovnik M, Thurnau GR, Goldenburg RL, Das AF, et al. The impact of digital cervical examination on expectantly managed preterm rupture of membranes. Am J Obstet Gynecol 2000; 183: 1003-1007. | ||
In article | CrossRef | ||
[10] | ACOG Committee on Practice Bulletins –Obstetrics, authors. Clinical Management guidelines for Obstetrician-Gynecologists. (ACOG Practice Bulletin No 80: premature rupture of membranes). Obstet Gynecol 2007; 109: 1007-1019. | ||
In article | CrossRef | ||
[11] | Mercer BM. Preterm premature rupture of the membranes: current approaches to evaluation and management. Obstet Gynecol Clin North Am 2005; 32:411-428. | ||
In article | CrossRef | ||
[12] | Di Renzo GC, Roura LC. The European Association of Perinatal Medicine – Study Group on Preterm Birth, authors. Guidelines for the management of spontaneous preterm labor. J Perinat Med 2006; 34: 359-366. | ||
In article | CrossRef | ||
[13] | Schrag S, Gorwitz R, Fultz–Butts K, Schuchat A. Prevention of perinatal group B streptococcal disease. MMWR Recomm Rep 2002;51:1-22 | ||
In article | |||
[14] | ACOG, authors, prevention of early–onset group B streptococcal disease in newborns (ACOG Committee Opinion: NO 279, December 2002). Obstet Gynecol 2002; 100: 1405-1412. | ||
In article | CrossRef | ||
[15] | Crowley P. Prophylactic corticosteroids for preterm birth. Cochrane Database Syst Rev. 2000: 2CD000065. | ||
In article | |||
[16] | Egarter C, Leitich H, Karas H, Wieser F, Hussiein P, Kader A, et al. Antibiotic treatment in preterm premature rupture of membranes and neonatal morbidity: a metaanalysis. Am J Obstet Gynecol 1996; 174: 589-597. | ||
In article | CrossRef | ||
[17] | Meis PJ, Emen–JM, Moore ML. Causes of Low birth weights in public and private patients. Am J Obstet Gynecol 1987; 156:1165-1168. | ||
In article | CrossRef | ||
[18] | Stuart EL, Evans GS, Lin YS, Powers HJ. Reduced collagen and ascorbic acid concentrations and increased proteolytic susceptibility with prelabor fetal membrane rupture in women. Biol Reprod 2005; 72:230-235. | ||
In article | CrossRef | ||
[19] | Babson SG, Benson RC. Management of high risk pregnancy and intensive care of the neonate. The C.V Mosby company. 1971; 54-56. | ||
In article | |||
[20] | Vermillion ST, Soper DE, Chasedunn-Roark J. Neonatal sepsis after betamethasone administration to patients with preterm premature rupture of membranes. Am J Obstet Gynecol 1999; 181: 320-327. | ||
In article | CrossRef | ||
[21] | Yoon BH, Kim YA, Romero R, Kim JC, Park KH, Kim MH, et al. Association of oligohydramnios in women with preterm premature rupture of membranes with an inflammatory response in fetal, amniotic and maternal compartments. Am J Obstet Gynecol, 1999; 181:784-788. | ||
In article | CrossRef | ||
[22] | Davidson KM, Detection of premature rupture of the membranes Clin Obstet Gynecol 1991; 34: 715-722. | ||
In article | CrossRef | ||
[23] | Harding JE, Pang J, Knight DB, Liggins GC. Do antenatal corticosteroids help in the setting of preterm rupture of membranes? Am J Obstet Gynecol 2001; 184: 131-139. | ||
In article | CrossRef | ||
[24] | Elimian A, Verma U, Beneck D, Cipriano R, Visintainer P, Tejani N. Histologic chorioamnionitis, antenatal steroids and perinatal outcomes. Obstet Gynecol 2000; 96:333-336. | ||
In article | CrossRef | ||
[25] | Dexter SC, Pinar H, Malee MP, Hogan J, Carpenter MW, Vohr BR. Outcome of very low birth weight infants with histopathologic chorioamnionitis. Obstet Gynecol 2000; 96:172-177. | ||
In article | CrossRef | ||