Contraception use and pregnancy in women receiving a 2-dose Ebola vaccine in Rwanda: A retrospective analysis of UMURINZI vaccination campaign data.

Publication date: Feb 01, 2025

Rwandan individuals bordering the Democratic Republic of the Congo (DRC) are at-risk of Ebola virus disease. A 2019 to 2021 vaccination campaign called UMURINZI offered a Janssen Vaccines & Prevention B. V. 2-dose heterologous Ebola vaccine regimen (Ad26. ZEBOV, MVA-BN-Filo) to Rwandan individuals aged ≥2 years and not pregnant. In this region with high rates of pregnancy, preventing pregnancy until their second dose of the Ebola vaccine is essential to ensure full protection. This analysis describes contraceptive use, pregnancy incidence, serious adverse events (SAE), and the effect of pregnancy and SAE on receipt of the second dose among women in the UMURINZI vaccination campaign. During the vaccination campaign, women who were fertile and sexually active were counseled as part of the campaign by trained UMURINZI nursing staff about preventing pregnancy until dose two (56 days post-dose one) and offered contraception. Women were followed up to their second dose appointment. Contraception, pregnancy incidence, and SAE were recorded. Of the 47,585 fertile and sexually active women, the mean age was 28.0 years (standard deviation 9.9 years), 54.7% (n = 26,051) were from Rubavu and 45.3% (n = 21,534) were from Rusizi, and 71.9% (n = 34,158) had not crossed the DRC border in the last year. Sixty-six percent (66.6%, n = 31,675) were not using modern contraception at baseline and 19.1% (n = 9,082) were using hormonal implants, 10.9% (n = 5,204) injectables, 2.9% (n = 1,393) oral contraceptive pills (OCPs), and 0.5% (n = 231) intrauterine devices. After contraceptive counseling, 8.0% (n = 2,549) of non-users initiated a method of contraception and 3.6% (n = 50) of OCP users switched to a more effective method. Of the 969 incident pregnancies detected after dose one, 18.8% (n = 182) resulted in an obstetric SAE, primarily due to spontaneous abortion which occurred in 16.0% (n = 155) of all incident pregnancies. Other obstetric SAE included 14 blighted ova, 9 stillbirths, 1 termination due to hydrops fetalis, 1 cleft palate, and 2 threatened abortions resulting in normal deliveries. Six pregnant women had a non-obstetric SAE (0.6%), including 1 postpartum death from COVID-19 and 5 hospitalizations. Among the 74,002 women without an incident pregnancy detected after dose one, 0.01% (n = 4) had an SAE; 2 were fatalities due to hypertension and diabetes in one case and seizures in the other, and the other 2 were hospitalizations. No SAE were determined to be related to the vaccine by the program physicians. Among the 74,002 women without an incident pregnancy detected after dose one, 94.6% (n = 69,986) received dose two; in contrast, among the 969 women with an incident pregnancy detected after dose one, 34.5% (n = 334) received dose two after pregnancy completion. Many fertile and sexually active women who sought vaccination during UMURINZI were not using contraception prior to vaccination, and contraceptive method uptake after family planning counseling and method provision was low. Most women who became pregnant after the first vaccination dose did not receive the second dose, thus potentially reducing protection against Ebola. Family planning messaging for this context should be developed and pilot-tested. The estimated risk of spontaneous abortion was similar to previous estimates from Rwanda and other African countries.

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Concepts Keywords
Abortion Adolescent
Diabetes Adult
Rwanda Contraception
Trained Contraception Behavior
Ebola Vaccines
Ebola Vaccines
Female
Hemorrhagic Fever, Ebola
Humans
Immunization Programs
Pregnancy
Retrospective Studies
Rwanda
Vaccination
Young Adult

Semantics

Type Source Name
disease MESH Ebola virus disease
drug DRUGBANK Etoperidone
disease MESH spontaneous abortion
disease MESH stillbirths
disease MESH hydrops fetalis
disease MESH cleft palate
disease MESH threatened abortions
disease MESH death
disease MESH COVID-19
disease MESH hypertension
disease MESH seizures
disease MESH Amelia
pathway REACTOME Reproduction
disease MESH Thrombocytopenia
disease MESH Syndrome
disease IDO country
disease MESH emergency
drug DRUGBANK Trestolone
disease IDO history
disease MESH allergies
disease IDO site
disease IDO facility
disease MESH pregnancy outcomes
disease MESH abnormalities
disease IDO symptom
disease MESH birth defect
disease IDO intervention
disease MESH adverse drug reactions
drug DRUGBANK Copper
drug DRUGBANK Coenzyme M
disease MESH deep vein thrombosis
disease MESH pharyngitis
disease MESH urinary tract infections
disease MESH arthralgia
disease MESH cholera
disease MESH schistosomiasis
disease MESH onchocerciasis
disease MESH lymphatic filariasis
disease MESH vaccine preventable diseases
disease MESH Viral Infections
drug DRUGBANK Diethylstilbestrol
disease MESH Unintended Pregnancy
disease MESH bleeding
drug DRUGBANK Hexocyclium

Original Article

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