Evidence map›Paper›PMID 41199993›Full record

ArticlePublic health challenges2025

Exploring the Lived Experiences of Adults With Sickle Cell Disease in Nigeria Using van Manen's Phenomenological Approach.

Florence Idowu Michael, Chinomso Nwozichi, Omolabake Salako, Mosidat Oshodi-Bakare, Elizabeth Olaogun, Josiah Nang-Bayi

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Article in Public health challenges, 2025. 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Florence Idowu MichaelDepartment of Nursing, School of Nursing Babcock University Ilisan Remo Ogun State Nigeria.
Chinomso NwozichiWellstar School of Nursing Kennesaw State University Kennesaw Georgia USA.
Omolabake SalakoOncology Nursing Society of Nigeria Ilisan Remo Ogun State Nigeria.
Mosidat Oshodi-BakareDepartment of Nursing, School of Nursing Babcock University Ilisan Remo Ogun State Nigeria.
Elizabeth OlaogunDepartment of Nursing, School of Nursing Babcock University Ilisan Remo Ogun State Nigeria.
Josiah Nang-BayiSunyani SDA Hospital Sunyani Ghana.ORCID https://orcid.org/0000-0002-7638-3496

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: This study explores the lived experiences of adults with sickle cell disease (SCD) in Ilorin, Kwara State, Nigeria, providing insights into their struggles and coping mechanisms. Design: A qualitative phenomenological study was conducted to gain a deeper understanding of the lived experiences of adults with SCD. Methods: This study employed a phenomenological approach to explore the lived experiences of adults with SCD. Semi-structured interviews were conducted with 24 participants, selected through purposive sampling. Data were analyzed thematically using van Manen's phenomenological approach to capture the depth of participants' experiences. Findings: Findings revealed that adults with SCD endure recurrent pain crises, emotional distress, stigmatization, and substantial financial burdens. Participants reported difficulties in accessing specialized healthcare, leading to increased reliance on alternative treatment methods. Social support was often inadequate, with many experiencing isolation and discrimination. Coping strategies identified included spiritual reliance, engagement in peer support networks, and self-management practices. Conclusions: The study underscores the urgent need for comprehensive healthcare interventions, improved psychosocial support systems, and public health policies tailored to the unique challenges faced by adults with SCD. Addressing these issues through multidisciplinary approaches can enhance the quality of life for individuals living with SCD in Nigeria and similar settings. Clinical Evidence: The findings highlight critical areas for healthcare improvement, including the need for accessible specialized care, financial support mechanisms, and community-driven psychosocial interventions. Integrating culturally relevant coping strategies, such as spiritual support and peer networks, into healthcare services may improve patient outcomes and overall well-being.

Indexed as

lived experiencesNigeriaphenomenologysickle cell disease

Identifiers

PMID41199993
PMCPMC12588339

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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.