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dc.contributor.authorLuggya, Anne Gladys
dc.date.accessioned2022-12-28T09:30:21Z
dc.date.available2022-12-28T09:30:21Z
dc.date.issued2022-11
dc.identifier.citationLuggya, A.G. (2022). Assessment of the quality of informed consent process for elective gynaecological and obstetric surgical procedures in Kawempe National Referral Hospital. (Unpublished masters dissertation). Makerere University, Kampala, Uganda.en_US
dc.identifier.urihttp://hdl.handle.net/10570/11254
dc.descriptionA research dissertation submitted to the Directorate of Research and Graduate Training at Makerere University in partial fulfillment for the award of Master of Medicine in Obstetrics and Gynaecologyen_US
dc.description.abstractBackground: The WHO declaration on patients’ rights, the patient has to be fully informed about their health status and medical facts. Obtaining informed consent is to respect patient’s autonomy, therefore it’s more than just a patient’s signature on paper. Informed consent for elective gynaecological or obstetric surgeries is required to improve compliance. The study aimed to assess the quality of informed consent process among patients undergoing elective gynaecological and obstetric surgery at Kawempe National Referral Hospital. Methods: A cross sectional study was conducted among patients who had undergone elective gynaecological and obstetric surgery at Kawempe National Referral Hospital. A total of 130 patients were recruited by systematic random sampling. Quality of informed consent was determined using a 5-point Likert scale. The cut off score for poor quality was ≤ 3. Analyzed data with STATA 16. Used Chi-square to test the association between clinical and demographic characteristics and the quality of informed consent. Used logistic regression to analyze the factors associated with poor quality. P- value ˂0.05 was statistically significant. Results: The mean age of participants was 30.6 years with IQR of 25 -33 years. Most participants 103/130 (79.23%) had poor quality of informed consent. The factors associated with poor quality were: lower education level (aPR=4.71 95% CI: 2.76-15.98 p = ˂ 0.0001), not aware that consent was required (aPR=2.18 95% CI: 1.20-5.21, p = 0.012), not aware that consent was voluntary (aPR=2.01, 95% CI: 1.18-6.26, p=0.017), using English language (aPR=2.64, 95% CI: 1.12-6.73, p=0.022) an interpreter (aPR=3.11, 95% CI: 1.22-7.43, p=0.015), and words only (aPR=2.42, 95% CI: 1.27-9.69, p=0.019). Consenting on ward (aPR=1.96, 95% CI: 1.22-6.18, p=0.028), short time to discuss (aPR=2.76, 95% CI: 1.22-8.01, p=0.022). Not asking questions (aPR=2.11, 95% CI: 1.15-12.32, p=0.018) and not reading the consent form (aPR=2.32, 95% CI: 1.19-9.02, p=0.028). Most participants (86%) had a friendly and empathetic communication with their clinicians. Conclusions: Majority of patients get poor quality informed consent prior surgery especially those with low education. Recommendations: Health workers communicate the purpose of informed consent to patients. KNRH should follow the national guidelines for obtaining informed consent. A study to assess the knowledge of health workers on informed consent process in this setting is recommended.en_US
dc.description.sponsorshipFogarty International Center of the National Institutes of Health, US and HEPI- SHSSUen_US
dc.language.isoenen_US
dc.publisherMakerere Universityen_US
dc.subjectInformed consent processen_US
dc.subjectelectiveen_US
dc.subjectGynaecologicalen_US
dc.subjectObstetricen_US
dc.subjectsurgeryen_US
dc.subjectKawempe National Referral Hospitalen_US
dc.titleAssessment of the quality of informed consent process for elective gynaecological and obstetric surgical procedures in Kawempe National Referral Hospitalen_US
dc.typeThesisen_US


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