Evidence map›Paper›PMID 41689050›Full record

ArticleBMC women's health2026

Predictors of delay in the cervical cancer care cascade in Kampala, Uganda.

Megan Swanson, Alison El Ayadi, Miriam Nakalembe, Jane Namugga, Carol Nakisige, Lee-May Chen, Megan J Huchko

Abstract read
In one paragraph

Article in BMC women's health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Megan SwansonDepartment of Obstetrics and Gynecology and Reproductive Sciences, Division of Gynecologic Oncology, University of California, San Francisco, CA, USA. megan.swanson@ucsf.edu.
Alison El AyadiDepartment of Obstetrics, Gynecology and Reproductive Sciences, Bixby Center for Global Reproductive Health, University of California, San Francisco, CA, USA.
Miriam NakalembeDepartment of Obstetrics and Gynaecology, Infectious Disease Institute, Makerere University College for Health Sciences School of Medicine, Kampala, Uganda.
Jane NamuggaDepartment of Obstetrics and Gynaecology, Division of Gynaecologic Oncology, Mulago Specialised Women and Neonatal Hospital, Kampala, Uganda.
Carol NakisigeDivision of Gynaecologic Oncology, Uganda Cancer Institute, Kampala, Uganda.
Lee-May ChenDepartment of Obstetrics and Gynecology and Reproductive Sciences, Division of Gynecologic Oncology, University of California, San Francisco, CA, USA.
Megan J HuchkoDepartment of Obstetrics and Gynecology, Center for Global Reproductive Health, Global Health Institute, Duke University, Durham, NC, USA.

Funding

University of California Global Health Institute Program for Fellows and ScholarsR25TW009343 · FIC · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COHEN, CRAIG R, STRATHDEE, STEFFANIE A. · 2012 to 2017
$6.4M
FIC NIH HHS R25 TW009343Fogarty International Center at the U.S. National Institutes of Health R25TW009343
6 · The paper itself

Abstract

backgroundCervical cancer is the fourth most common cancer among women with significant global disparities in disease burden. In lower-resource settings, where routine screening for cervical cancer is uncommon, higher incidence of advanced-stage disease contributes to increased morbidity and mortality. Understanding care delays may inform strategies to decrease overall time to treatment, and could potentially improve outcomes. We sought to characterize the cervical cancer care cascade and identify factors associated with time to care cascade completion within a Ugandan cohort.

methodsWe collected sociodemographic, reproductive health and care journey data from 268 Ugandan women newly diagnosed with cervical cancer at Mulago National Referral Hospital and the Uganda Cancer Institute. We characterized time from symptoms to presentation (patient interval), time from presentation to diagnosis (diagnostic interval) and time from diagnosis to treatment (treatment interval) and estimated the influence of patient, health provider, system, and disease factors on length of each interval using survival analysis.

resultsMedian patient, diagnostic and treatment intervals were 74 days (IQR 26–238), 83 days (IQR 34–229), and 34 days (IQR 18–58), respectively. Patient interval was prolonged by the belief that symptoms would resolve spontaneously (aHR 0.37, 95% CI 0.24–0.57), confusion about where to seek care (aHR 0.64, 95% CI 0.47–0.88), and utilization of traditional care (aHR 0.70, 95% CI 0.51–0.96). Patient interval facilitators included perceiving symptoms as serious (aHR 2.14, 95% CI 1.43–3.19) and suspecting cancer (aHR 1.82, 95% CI 1.12–2.97). Diagnostic interval delays included symptomatic bleeding (aHR 055, 95% CI 0.35–0.85) and visiting > 2 clinics (aHR 0.69, 95% CI 0.49–0.97); facilitators included early-stage disease (aHR 1.41, 95% CI 1.03–1.95) and direct tertiary care presentation (aHR 2.13, 95% CI 1.20–3.79). Treatment interval delays included anticipating long waits (aHR 0.68, 95% CI 0.46–1.02) and requiring blood transfusions (aHR 0.63, 95% CI 0.37–1.07); no facilitators were identified.

conclusionsWe identified potentially modifiable barriers and facilitators along the cervical cancer care cascade. Interventions targeting these factors may reduce delays, but are unlikely to significantly improve morbidity or mortality given advanced-stage disease at symptom acknowledgement and relatively timely treatment initiation. Expanding cervical cancer screening and vaccination are of utmost importance.

Indexed as

Delayed DiagnosisTime-to-TreatmentUterine Cervical NeoplasmsAdultEarly Detection of CancerFemaleHumansMiddle AgedPatient Acceptance of Health CareTreatment DelayUgandaCervical cancerDelayResource-limited settingsTreatment access

Identifiers

PMID41689050
PMCPMC13005556

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.