Introduction. Integrated use of postpartum intrauterine contraceptive devices with delivery service during the immediate postpartum period is ideal for both women and health-care providers. However, utilization of intrauterine contraceptive devices during the postpartum period was rare and in Ethiopia, with information regarding uptake of postpartum intrauterine contraceptive devices limited. Objective. Identify determinants of postpartum intrauterine contraceptive devices uptake among women delivering in public hospitals of South Gondar zone, Northwest Ethiopia, 2019. Methods. An unmatched case-control study was conducted in public hospitals of South Gondar, Ethiopia, from August 1, 2019, to November 10, 2019. A total of 140 cases and 280 controls have actively participated in the study. Five hospitals were selected by simple random sampling. Cases were selected consecutively, whereas two controls for each case were recruited by the lottery method. Pretested questionnaires were used to collect data and it was entered into Epidata version 4.4.2. Logistic regression analysis was used to identify variables associated with the use of outcome and adjusted odds ratio with a 95% confidence interval was used to determine the association between independent and outcome variables. Results. Completing secondary education (AOR = 4.5, 95%CI 2.3-8.85), having a total number of children of 3-4 (AOR = 3.6, 95%CI 1.25-10.2), having ≥ 5 (AOR = 4.7, 95%CI 1.5-15.3), attending 3 antenatal care (AOR = 2.8, 95%CI 1.44-5.6), ever hearing about postpartum IUCD (AOR = 6.6, 95%CI 2.7-16.1), and having counseling from health-care provider about a postpartum intrauterine contraceptive device (AOR = 6.2, 95%CI 2.99-12.8) were significantly associated with uptake of the postpartum intrauterine contraceptive. Conclusion and Recommendation. Completing secondary education, having 3-4 and ≥5 children, attending three antenatal care, ever hearing about postpartum IUCD, and having counseling from health-care providers about the postpartum intrauterine contraceptive device among women were significantly associated with uptake of an intrauterine contraceptive device after birth. Therefore, it is better to advise women to strictly follow their antenatal care, access to information, and provide counseling.
An unmatched case-control study was conducted in South Gondar zones public hospitals such as Debretabor general hospital, Mekane-eyesuse primary hospital, Wogeda primary hospital, Addis Zemen primary hospital, and Nifas Mewucha primary hospital from August 1, 2019, to November 10, 2019. South Gondar is one of the zones found in Amhara region and its capital city is Debretabor, which is found 666 km far from Addis Ababa, capital city of Ethiopia. There are eight hospitals found in the zone, which serve 2,609,823 populations. Other maternal and family planning services were given without payment in all public hospitals. Currently, CUT 380 PPIUCD is available in all hospitals. A facility-based unmatched case-control study design was conducted. The source population is all postpartum women who gave birth in public hospitals of South Gondar zone, during the study period. All postpartum women delivering in selected public hospitals during the study period and using a postpartum intrauterine contraceptive device within the first 48 hours following vaginal delivery and intracaesarean after the expulsion of the placenta before uterine closure were considered as cases. However, all postpartum women who gave birth in the same hospitals but did not use postpartum intrauterine contraceptive devices were considered as controls. Postpartum women who gave birth by any mode of delivery in the selected public hospitals were included. Women who gave birth by any mode of delivery in selected public hospitals but did not fulfill WHO medical eligibility criteria for PPIUCD during the study period were excluded [9]. The sample size for the study was determined with double population proportion formula by using Epi info version 7 statistical software program for an unmatched case-control study. The calculation considered the following assumptions: 95% confidence interval, 80% power, 1 : 2 ratio of cases to controls, with a plan to have another child as the exposure variable, 47.7% of PPIUCD users and 32.8% of nonusers with exposure [7], and 10% nonresponse rate as compensation for both groups. Therefore, 450 postpartum women (150 cases and 300 controls) were included in the study. The sample size for each selected public hospital was proportionally allocated based on previous monthly average PPIUCD utilization. In south Gondar, there are eight hospitals, and about five (63%) of them were selected by simple random sampling methods. Then the number of PPIUCD utilizations per three months was obtained from each selected public hospital’s quarterly report to calculate average monthly cases flow. Cases were identified by asking them whether or not they use IUCD after delivery and by crosschecking their charts and they were selected consecutively, and as soon as cases were identified two controls were selected by simple random methods to increase the power of the study. Uptake of a postpartum intrauterine contraceptive device was a dependent variable. Data were collected using a pretested, semistructured, and interviewer-administered questionnaire. The questionnaire was adapted by reviewing similar researches conducted previously [5–7, 10–12]. The questionnaire involves sociodemographic, obstetric, reproductive, maternal health care, and family planning-related variables. Initially, the questionnaire was prepared in the English version then it was translated into the local language. Five trained BSc midwives and two BSc nurses have participated in data collection and supervisor, respectively. One data collector was assigned to each hospital. To assure the quality of data, the tool was tested by interviewing 5% of postpartum women who gave birth at Gina Mechawocha and Este health center two weeks before the actual data collection and a necessary correction was applied. Half-day training had been given for data collectors and supervisors about the purpose of the study, data collection procedures, and ways of communicating by the principal investigator. Continuous observation of the data collection process and its completeness was assessed every two weeks. At the end of data collection, completeness of data was checked; coding was implemented and entered into Epidata version 4.4.2.1. Statistical software and exported to SPSS version 23 software for further analysis. Descriptive variables were presented using tables and charts. Bivariate binary logistic regression was used to assess the association between PPIUCD uptake and each factor separately. All variables with p value less than or equal to 0.2 in the bivariate logistic regression were entered into the multivariable logistic regression model. Multivariable logistic regression was done by using a backward likelihood ratio method to control potential confounders. Correlation between independent variables was done to check multicollinearity. Finally, the adjusted odds ratio with 95% confidence interval was determined to measure the strength of association, and a p value less than 0.05 was used to determine the significant association between factors and outcome variables. The study obtained ethical clearance from the research review commute of the school of midwifery on behalf of the University of Gondar ethical review board. Written permission was obtained from the responsible body of the South Gondar zone health office and each selected hospital’s medical director after approval consent letter was submitted. Verbal informed consent was secured, after the purpose of the study was explained to each study participant.
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