Evidence map›Paper›PMID 42290336›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia

Perceived Barriers to Healthcare Access Among Paediatric Patients With Haemophilia in Cambodia: A Cross-Sectional Survey.

Chean Sophâl, Heng Sivmeng, Lean Kimsreng, Ith Ponndara

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Article in Haemophilia : the official journal of the World Federation of Hemophilia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Chean SophâlDepartment of Pediatric Hematology and Immunology, Hemophilia Treatment Center, National Pediatric Hospital, Phnom Penh, Cambodia.ORCID https://orcid.org/0009-0000-6954-0492
Heng SivmengDepartment of Pediatric Hematology and Immunology, Hemophilia Treatment Center, National Pediatric Hospital, Phnom Penh, Cambodia.
Lean KimsrengTechnical Office, National Pediatric Hospital, Phnom Penh, Cambodia.
Ith PonndaraAcademic and Training Office, University of Health Sciences, Phnom Penh, Cambodia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHaemophilia is a rare inherited bleeding disorder, and in low- and middle-income countries, care is often limited by delayed diagnosis and restricted access to specialised services. In Cambodia, care is centralised in only two treatment centres, which may further limit timely diagnosis and treatment.

aimTo assess perceived barriers to healthcare access among paediatric patients with haemophilia in Cambodia.

methodsA cross-sectional survey was conducted in Cambodia from July to December 2025 among 100 reachable patients aged ≤18 years with Haemophilia A or B from a National Hemophilia Registry of 250 patients. Data were collected through telephone or face-to-face interviews using a structured questionnaire administered primarily to parents or caregivers.

resultsAmong 100 participants, 88% reported at least one diagnostic barrier, mainly limited caregiver knowledge, difficulty accessing experienced providers, and delayed referral. Barriers to daily home-based bleeding management were reported by 83%, largely related to inadequate caregiver education and limited healthcare support. Barriers to accessing haemophilia treatment centres affected 73%, mainly geographic distance, financial constraints and transportation difficulties. Delays in receiving treatment were reported by 69% and were significantly associated with clotting factor shortages, financial constraints and delayed referral. Clotting factor shortage was not significantly associated with home-based management barriers but contributed to treatment delays. Most participants reported satisfaction with care (82%) and perceived care as equitable (85%).

conclusionPaediatric haemophilia care in Cambodia is limited by geographic, financial, educational and health-system barriers. Improving education, referral pathways, home-care support, clotting factor supply and financial protection may strengthen care access.

Indexed as

Health Services AccessibilityHemophilia AAdolescentCambodiaCaregiversChildChild, PreschoolCross-Sectional StudiesFemaleHumansInfantMaleSurveys and QuestionnairesbarriersCambodiahaemophiliahealthcare accesssocio‐economic factors

Identifiers

PMID42290336
PMCPMC13551269

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