Background Primary postpartum hemorrhage is the leading cause of maternal mortality worldwide. Ethiopia has made significant progress in maternal health care services. Despite this, primary postpartum hemorrhage continues to remain the leading cause of maternal mortality in Ethiopia. This study aimed to assess the prevalence and predictors of primary postpartum hemorrhage among mothers who gave birth at selected hospitals in the Southern Ethiopia. Methods An institution-based cross-sectional study was employed from March 2–28, 2018. Four hundred and twenty-two study participants were obtained using the consecutive sampling method. A structured interviewer-administered questionnaire and chart review were used to collect data. Data were entered into Epi-data version 3.1 and analyzed using SPSS version 22. Multivariable logistic regression were used to determine the predictors of primary postpartum hemorrhage with 95% CI and p-value < 0.05. Results The overall prevalence of primary postpartum hemorrhage was 16.6%. Mothers aged 35 and above [AOR = 6.8, 95% CI (3.6, 16.0)], pre-partum anemia [AOR = 5.3, 95% CI (2.2, 12.8)], complications during labor [AOR = 1.8, 95% CI (2.8, 4.2)], history of previous postpartum hemorrhage [AOR = 2.7, 95% CI (1.1, 6.8)] and instrumental delivery [AOR = 5.3, 95% CI (2.2, 12.8)] were significant predictors of primary postpartum hemorrhage. Conclusion Primary postpartum hemorrhage is quite common in the study area. Mothers aged 35 and above, complications during labor, history of previous postpartum hemorrhage, and instrumental delivery were predictors of primary postpartum hemorrhage. Since postpartum hemorrhage being relatively common, all obstetrics unit members should be prepared to manage mothers who experience it.
It was an institution-based cross-sectional conducted in the Wachemo University Negist Eleni Mohammed Memorial General Hospital, Butajira Zonal Hospital and in the Worabe comprehensive Hospital from March 2–28, 2018. Source populations were all mothers who gave birth in the selected Hospitals during the study period and mothers who cannot able to communicator critically ill/sick at the time of data collection were excluded from the study. The single population proportion formula was used to determine sample size with the following assumptions: prevalence of primary postpartum hemorrhage was 50%, 95% confidence interval, marginal error 5% and 10% none response rate, the final sample size was 422. Three hospitals were selected purposely. From all hospitals, 422 participants were selected using a consecutive sampling technique till the calculated sample size was achieved. The allocation of the study participants to each hospital was based on the previous monthly deliveries (from hospital records). Data were collected using a pretested structured interviewer administered questionnaire and patient's chart reviewed, which was used to retrieve diagnosis of primary postpartum hemorrhage and mothers’ test results that could not be captured by the interview. Research questionnaire was developed based on the instruments that were applied in other related studies [11, 14, 24–26]. It was intended to collect data on sociodemographic variables, obstetric related characteristics (antepartum, intrapartum and postpartum events) and fetal factors. Three B.Sc. midwives, and one M.Sc. midwife were recruited for the data collection and supervision, respectively in each hospital. To ensure the quality of data collected from the study participants, at the beginning, a data collection questionnaire was pre-tested on 5%(21) of calculated sample size at the Halaba Zonal Hospital and necessary modifications were made based on gaps identified in the questionnaire. Data collectors and supervisors were trained for three days intensively on the study instrument and data collection procedure that includes the relevance of the study. The English questionnaire was translated first to the local language and translated back into English language by experts to check its consistency. The data collectors worked under close observation of the supervisors to ensure reliability to correct data collection procedures. In addition, supervisors and the principal investigators checked the filled questionnaires at the end of data collection every day for completeness. Furthermore, the data were carefully entered and cleaned before the beginning of the analysis. In this study the definition of clinical diagnosis PPH was obtained from the mothers’ card which was identified by birth attendants and was classified as: “yes” (having a clinical diagnosis of postpartum hemorrhage in the mothers’ card) or “no”. Such as antepartum hemorrhage, hypertension disorders during pregnancy, polyhydramnios, chorioamnionitis or/and others. Malpresentation, malposition, prolonged labour or obstructed labour, or/and others, (present = 1 or absent = 0). Data were entered using Epi-data version 3.1 and exported to statistical package social science (SPSS), version 22.0 software for analyses. Multivariable logistic regression was done for variables that have p-value ≤ 0.25 during the bivariate logistic regression analyses to identify the predictor of PPH and to control for potential confounders. The degree of association between independent, and dependent variables were assessed using odds ratio with 95% confidence interval. The P-value 0.05 which proved the model was good. Ethical approval was taken from the Institutional Review committee of Wachemo University. Formal letters were obtained from the Hadiya, Silte and Gurage zonal health office administration. Then, permission was obtained from each hospital authority before commencing the data collection. The participants were informed about purpose, procedures, potential risks and benefits of the study. Informed written consent was sought from selected participant to confirm willingness to participate in the study before the interview. To protect confidentiality, name was not included in the written questionnaire. The study participants also were ensured that refusal to consent or withdrawal from the study would not alter or put at risk their access to care.