Background: Stillbirth is one of the adverse outcomes of pregnancy, and it is among the major public health problems in developing countries including Ethiopia. Stillbirth has wide-reaching consequences for parents, care providers, community and society at large. Purpose: To assess the determinant of stillbirth among deliveries attended in Bale zone hospitals Southeast Ethiopia. Methods: An institution-based unmatched case–control study was conducted. Cases were deliveries whose birth outcome was stillbirth and controls were deliveries with live birth. A pretested and structured checklist was used to collect data from a sample of 402 (134 cases and 268 controls). Systematic random sampling was used to recruit samples from a list of charts in the delivery registration book. Data were entered into EpiData version 4.2 and exported to SPSS version 20 for analysis. Crude and adjusted odds ratio with 95%CI was calculated and P-value <0.05 was used to declare statistical significance. Results: A total of 402 charts of mothers (134 cases and 268 controls) were included in the analysis. Preceding birth interval <24 months (AOR: 2.991; 95%CI: 1.351–6.621), antenatal visit started at third trimester (AOR: 2.739; 95%CI: 1.048–7.158), referred from other health facility (AOR: 3.215; 95%CI: 1.430–7.229), labor length ≥24 h (AOR: 3.169; 95%CI: 1.241–8.091), presence of meconium stained amniotic fluid (AOR: 2.670; 95%CI: 1.082– 6.592) and giving birth to a baby <2500 g (AOR: 3.155; 95%CI: 1.235–8.07) were determinants of stillbirth. Conclusion: Preceding birth interval of <24 months, antenatal visit started at third trimester, referred from other health facility, presence of meconium stained amniotic fluid, labor length ≤24 h and giving birth to a baby <2500 g were found the determinants of stillbirth. Intrapartum care, early identification of labor complications and referral system are required.
The study was conducted at the five public hospitals found in Bale zone. Bale zone is located in Oromia regional state in Southeast Ethiopia. Robe town, the capital of Bale zone is found 430 km away from Addis Ababa, the capital city of Ethiopia. Currently, the zone has 21 districts of which three are town administrations and of the rural districts nine are agrarian and nine are agro-pastoralist. The zone has a total population of 1,888,366 of which 951,736 are male, 936,630 are female and the expected deliveries in the study year accounts are 65,526. A total of five public hospitals are found in the zone; namely Goba Referral Hospital, Robe General Hospital, Ginnir General Hospital, Dalo Mena General Hospital and Madda Walabu Primary Hospital. There are also 87 functional health centers in the zone. Concerning comprehensive maternal service delivery, all the hospitals deliver comprehensive emergency, obstetric, and neonatal care service and 76 health centers deliver basic emergency, obstetric and neonatal care services. The study was conducted from July 2018 to June 2019 and an institution-based unmatched case–control study design was employed. All charts of mothers who delivered from July 2018 to June 2019 in the five hospitals of Bale zone were the source population. All charts of mothers delivered from July 2018 to June 2019, which were selected by systematic random sampling as cases and controls in the five hospitals of Bale zone were the study population. Stillbirths whose charts are available and have full history recorded delivery summery and/or procedure notes during the study period were included in the study as cases. Live births, whose charts are available and have full history, delivery summery and or procedure notes during the study period were included in the study as controls. Twelve charts which were found incomplete on major variables under study (no information about antenatal period, labor status and/or delivery summary) and missed charts were excluded. Sample size is calculated using EpiInfo 7.0 StatCalc program by taking assumptions of 95% confidence level, two controls for each case, 80% power and the prevalence of exposure among control 7.1% with odds ratio 2.8 (1.78, 4.46) of variable low birth weight, were taken from an unmatched a case–control study done at Hawasa University Hospital, Ethiopia.12 A total sample size of 366 (122 cases and 244 controls) were calculated and adding 10% contingency for incomplete check list filled by data collectors and the final sample size was 402 (134 cases and 268 controls). A variable low birth weight was selected because it was the exposure variable that gave the highest sample size for cases and controls among the other variables in a study conducted in Hawasa University. The allocation of samples to each hospital was determined based on proportion of number of cases using report of the period (July 2018 – June 2019). Accordingly from Goba Referral Hospital 37 cases and 74 controls, Robe General Hospital 33 cases and 66 controls, Ginnir General Hospital 35 cases and 70 controls, Dalo Mena General Hospital 20 cases and 40 controls and Madda Walabu Primary Hospital nine cases and 18 controls were taken. Systematic random sampling with interval K=3 was used to recruit charts of cases after listing medical record numbers of all stillbirths in the study period from the delivery registration book of each hospital. Controls were also selected using systematic random sampling from the list of live births prepared from the delivery registration book and using the list as a sampling frame. Then, the selected charts, ie 134 for cases and 268 for controls were identified from the card room. The dependent variable for the study was stillbirth. And the independent variables were sociodemographic factors (age, residence, marital status), maternal health and pregnancy related factors (gravidity, parity, preceding birth interval, history of stillbirth, maternal medical illness, antenatal follow up, tetanus toxoid vaccination, iron folic acid supplementation, antepartum hemorrhage, hypertensive disorder of pregnancy, premature rupture of membrane), labor and delivery related factors (mode of admission, partograph use, fetal presentation, cord accident, obstructed labor, color of amniotic fluid, labor augmentation, duration of labor, mode of delivery) and fetal related factors (gestational age at birth, birth weight, number of newborns, congenital structure). Stillbirth: a baby born without any signs of life at or after 28 weeks of gestation or at least 1000 g in birth weight.1 Cases: were deliveries whose birth outcome was stillbirths, defined as babies born without any signs of life at or after 28 weeks of gestation or at least 1000 g in weight. Controls: were deliveries whose birth outcome of live births, defined as babies showing evidence of life (such as beating of the heart, pulsation of umbilical cord) on delivery at or after 28 weeks of gestation or at least 1000 g in weight. Partograph use: if the data on the three components of partograph (fetal condition, progress of labor, and maternal condition) were completed, it is considered that a partograph is utilized. Data was collected by using pretested and structured checklist which was developed in English language adapted from literature related to stillbirth and modified according to the local context by the investigators. The checklist consists of information on sociodemographic data, maternal health and pregnancy data, labor and delivery data and birth outcome data. Five data collectors who have midwifery profession were recruited for data collection and five senior midwives were also recruited for facilitation and supervision of daily data collection activities. During collection charts of cases and controls, the following steps were followed: first, all medical record numbers of stillbirths found in the study period were identified and listed from the delivery registration book of each hospital. Using a systematic random sampling method, cases were selected for each hospital proportionally to their annual stillbirth delivery load. Following selection of cases and controls, data collectors and card room workers have selected charts of mothers from card room using medial record numbers and reviewed the history, delivery summery, laboratory results, partograph, decision notes, progress notes, and operation notes and filled in the checklist. Incomplete charts on major variables under study (no information about antenatal period, labor status and/or delivery summary) were excluded. The selected charts were given study identification numbers to be used on the checklist for anonymity. Prior to data collection, the data collectors and supervisors were trained with a practical session for one day on techniques of sampling and data collection. Pretest was carried out on 5% of the samples before the actual data collection at Dodola General Hospital and modifications of the checklist were made on rephrasing and skipping patterns. In addition the average time required to complete one checklist was also estimated. Review of medical records was done carefully; charts with incomplete information on major variables under study such as information about antenatal period, labor status and/or delivery summary were excluded. Daily evaluation for completeness at the time of data collection was followed by the supervisor to assure collection of full information and appropriate documentation. The investigator has reviewed all checklists for omissions, clarity, and consistency of data to verify the completeness of the collected data. Data entering was performed using EpiData version 4.2 and coding, clearing and analysis was done using SPSS version 20 software statistical packages by the principal investigator. Frequency and proportions were used to describe the study population in relation to relevant variables. Those variables with a P<0.25 in the bivariate logistic regression analysis were entered to multivariate logistic regression analysis and declared significant at 95% confidence interval. Multiple logistic regression analysis was employed and significance was declared at P<0.05 and 95% confidence interval. Multicollinearity test was carried out to see the correlations between predictors of outcome variables. Finally the results were presented using tables and texts. Ethical clearance was secured and the official letter of permission was obtained from the Madda Walabu University, Goba Referral Hospital. Subsequently, a letter of permission was obtained from each hospital administrator and sent to each hospital maternal and child health units and medical record departments. The objective of the study was explained to the head of each unit and administrators of the hospitals. The permission of the patient to review their medical history was not required by the University of Madda Walabu and the hospitals. Personal identifiers such as name, phone number, etc have not been considered as a code and a care number has been used. At the end of the data collection process, strict attention was paid to the selected charts of study participants during the data collection phase, until the return was respected at the end of the data collection. All information taken from the client charts was kept confidential and only investigators had access to the information which was used only for the purpose of this study.
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