Medical Abortion Self-Use in Kenya: Results from a process evaluation of women's experiences

Abstract

Background The consequences of unsafe abortions weigh heavily on individuals, families, society, and health care systems. Developing countries continue to experience a high prevalence of mistimed and unintended pregnancies resulting in induced abortions that are largely unsafe. Globally, 25 million unsafe abortions take place every year [1]. In Africa, 3 out of 4 abortions are categorized as unsafe [2]. In Kenya, it is estimated that 464,690 induced abortions occur annually- 2 out of 3 of these are unsafe[3]. With the high prevalence of mistimed and unwanted pregnancies in Sub-Saharan Africa and Kenya in particular, unsafe abortions will be on the rise unless deliberate measures and policies are put in place to guarantee safe abortion procedures[4]. Method Ipas Africa Alliance embarked on the Medical Abortion Self-Use (MASU) project aimed at reducing morbidity and mortality tied to unintended pregnancies among women in the Counties of Vihiga, Kisumu, Busia, Siaya, and Trans Nzoia. To inform on the progress and the potential for scale-up of the project, Ipas commissioned a process evaluation. This evaluation adopted both qualitative and quantitative methods. This involved in-depth interviews (IDIs), Focus Group Discussions (FGDs), and face-face-interviews through a semi-structured questionnaire. Results From the analysis, those seeking medical abortion were mainly youths under 25 years of age. There was low awareness of safe abortion practices and the gestation period within which safe medical abortion (MA) can be safely done. Nearly half (47%) of the women and girls reported being coerced to take post-abortion contraceptives they never wanted. Further, MA costs were not only found to be expensive but also varied greatly across the Counties. Some MA users experienced medical complications attributed to the failure of pharmacists responsible to provide the correct dose and correct route of administration. On the other hand, youth champions were found to be few and not able to fully cover their areas and only have basic knowledge of MA self-use services. Conclusion The IPAS MASU project intervention, in the five counties of Western Kenya namely Busia, Siaya, Vihiga, Kisumu, and Trans Nzoia, has increased access to safe Medical Abortion self-use, enhanced availability of MA drugs in pharmacies, the improved service delivery of MA services through regular training of pharmacists. Further, the project has enhanced awareness about MA services among young girls and women through trained Youth Champions and pharmacists, and the MASU project has significantly reduced cases of unsafe abortions and by extension deaths and medical complications associated with them. To realize more gains, the project needs to be scaled up within the five counties and beyond, specifically to target the rural areas where cases of unsafe abortion are still thought to be rampant.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

No funding was obtained for this study instead it was an organizational unrestricted money.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study protocol was reviewed and approved by the Jaramogi Oginga Odinga Teaching and Referral Hospital (JOOTRH) Ethics and Scientific Research Committee, approval number: IERC/JOOTRH/464/21. Additional permits to conduct the study were obtained from the registered pharmacies’ proprietors and individual written consent was obtained from each FGD participant. During the informed consent process, data collectors emphasized to the participants that the study is voluntary and ensured that the participants understood the risks and benefits associated with the study and that they were ready and willing to participate. We do hereby confirm that all methods were carried out per relevant guidelines and regulations within the approved protocol.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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Yes

Data Availability

Data is available within the organization's cloud server and can be shared upon requests

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