Determinants and Experiences of Care-Seeking for Childhood Pneumonia in a Rural Indian Setting: A Mixed-Methods Study

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Barsha Gadapani Pathak, Sarmila Mazumder, Yasir Bin Nisar, Aditya Bhatt, Mandeep Singh, Tarun Madhur, Ingvild Fossgard Sandøy
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引用次数: 0

Abstract

Introduction

Pneumonia is a leading cause of under-five mortality, with 30 million annual cases in India. Despite national guidelines, significant barriers to timely and appropriate care-seeking persist. Caregivers often face financial constraints, lack of awareness, mistrust in government facilities and a preference for non-registered medical practitioners (non-RMPs), delaying effective treatment. This study explores care-seeking behaviours, associated socio-demographic factors and barriers to access to appropriate healthcare for childhood pneumonia in rural India.

Methods

This study is part of a broader implementation research (IR) initiative and represents its formative phase. This mixed-methods study was conducted in Palwal district, Haryana, covering 42 villages (population: 107,440). A cross-sectional survey identified suspected pneumonia cases among 9593 under-five children through house-to-house visits using a structured checklist. Data on socio-demographic characteristics, health insurance, care-seeking patterns and provider preferences were collected. Directed acyclic graphs (DAGs) identified potential confounders in the association between care-seeking behaviour and key exposure variables. Additionally, qualitative in-depth interviews explored caregivers' perceptions, decision-making and healthcare barriers to pneumonia management. Quantitative data were analysed using logistic regression, while qualitative data were thematically analysed using the Three Delays Model. Suspected under-five pneumonia cases' caregivers and families were actively engaged in this formative phase to inform Phase II implementation strategies of broader IR, ensuring community-driven and contextually relevant strategies.

Results

Among 231 suspected pneumonia cases, 97% of caregivers sought medical care, but 71% consulted non-RMPs, and only 3.6% visited government facilities. Seeking appropriate care was associated with higher maternal education (AOR 6.5, 95% CI: 2.7–9.7) and higher wealth index (AOR 1.7, 95% CI: 1.0–2.6). Thematic analysis revealed delays due to symptom misinterpretation, reliance on home remedies, financial constraints, gender biases, mistrust in public healthcare services and logistical barriers.

Conclusion

Despite high care-seeking rates, provider preferences, socio-cultural factors and systemic barriers delay appropriate pneumonia treatment. Addressing these challenges requires improving awareness, enhancing public healthcare trust and strengthening frontline healthworker engagement. This study underscores the role of structured beneficiary involvement in refining pneumonia management strategies to ensure sustainable, community-driven interventions.

Patient or Public Contribution

This study is part of an ongoing implementation research (IR) aimed at improving the effective coverage of childhood pneumonia management in a low-resource setting. A structured engagement with primary caregivers of under-five children, mothers, fathers, family members, community members and local community stakeholders/representatives, for example, local leaders, village heads and so forth, has been integrated at multiple stages to ensure the relevance and applicability of its findings. The current study is part of Phase I (formative research) of the IR, where primary caregivers and family members participated in a needs assessment, providing critical insights into the barriers and facilitators influencing care-seeking for childhood pneumonia in a rural low-to-middle socio-economic setting. Their inputs have informed the refinement of study tools and the development of mitigation strategies for the logic and implementation model. As the research progresses into Phase II (model development and implementation), the community continues to play an integral role in providing feedback on the feasibility and appropriateness of proposed strategies. This ongoing feedback loop assesses how effectively these strategies strengthen linkages between the healthcare system and the community, foster an active local needs assessment mechanism among healthcare providers and enhance demand generation for appropriate pneumonia care-seeking. These iterative refinements ensure that the implementation strategies remain responsive to the evolving needs of the community. In the forthcoming Phase III, which will focus on scaling up the finalised implementation model, strategies will be adapted to further improve care-seeking for under-five children. Continuous engagement with caregivers and local community representatives, including Panchayati Raj Institution (PRI) members, will be central to refining these strategies. Additionally, during the dissemination phase, key findings will be shared with caregivers, community members and PRI representatives, facilitating discussions on study implications and informing future policy and programmatic decisions. Their ongoing involvement will help contextualise findings and enhance the long-term sustainability of strategies aimed at improving pneumonia care-seeking behaviours and effective management in rural India.

印度农村儿童肺炎的决定因素和就医经验:一项混合方法研究
肺炎是五岁以下儿童死亡的主要原因,印度每年有3000万例病例。尽管有国家指导方针,但在及时和适当的求医方面仍然存在重大障碍。护理人员往往面临资金限制、缺乏认识、对政府设施的不信任以及对非注册医生(非rmps)的偏好,从而延误了有效治疗。本研究探讨了印度农村儿童肺炎的求医行为、相关社会人口因素和获得适当医疗保健的障碍。方法本研究是更广泛的实施研究(IR)倡议的一部分,代表了其形成阶段。这项混合方法研究在哈里亚纳邦帕尔瓦尔县进行,涵盖42个村庄(人口:107,440)。一项横断面调查通过使用结构化检查表挨家挨户访问,在9593名五岁以下儿童中确定了疑似肺炎病例。收集了有关社会人口特征、健康保险、求医模式和提供者偏好的数据。有向无环图(dag)确定了寻求护理行为和关键暴露变量之间关联的潜在混杂因素。此外,定性深入访谈探讨了护理人员对肺炎管理的看法、决策和卫生保健障碍。定量数据使用逻辑回归分析,而定性数据使用三延迟模型进行主题分析。疑似五岁以下肺炎病例的护理人员和家庭积极参与了这一形成阶段,为更广泛的第二阶段实施战略提供信息,确保社区驱动和与环境相关的战略。结果在231例疑似肺炎病例中,97%的护理人员就诊,71%的护理人员就诊于非护理人员,仅有3.6%的护理人员就诊于政府机构。寻求适当护理与较高的母亲教育程度(AOR 6.5, 95% CI: 2.7-9.7)和较高的财富指数(AOR 1.7, 95% CI: 1.0-2.6)相关。专题分析显示,延误是由于对症状的误解、对家庭疗法的依赖、财政限制、性别偏见、对公共保健服务的不信任和后勤障碍。结论尽管求诊率高,但提供者偏好、社会文化因素和系统性障碍等因素延误了肺炎的适当治疗。应对这些挑战需要提高认识,增强公众对卫生保健的信任,并加强一线卫生工作者的参与。本研究强调了受益人在完善肺炎管理策略以确保可持续的、社区驱动的干预措施中的作用。本研究是一项正在进行的实施研究(IR)的一部分,旨在提高低资源环境下儿童肺炎管理的有效覆盖率。与五岁以下儿童的主要照顾者、母亲、父亲、家庭成员、社区成员和当地社区利益相关者/代表(如当地领导人、村长等)的结构化接触已在多个阶段进行整合,以确保其调查结果的相关性和适用性。目前的研究是IR第一阶段(形成性研究)的一部分,其中主要照顾者和家庭成员参与了需求评估,为影响农村中低收入社会经济环境中儿童肺炎求医的障碍和促进因素提供了重要见解。他们的投入为改进研究工具和制定逻辑和实施模型的缓解战略提供了信息。随着研究进入第二阶段(模型开发和实施),社区继续发挥不可或缺的作用,就拟议战略的可行性和适当性提供反馈。这种持续的反馈循环评估这些策略如何有效地加强医疗保健系统与社区之间的联系,在医疗保健提供者之间建立积极的地方需求评估机制,并提高对适当的肺炎求诊的需求。这些迭代的改进确保了实施策略对社区不断变化的需求保持响应。在即将到来的第三阶段,其重点将是扩大最后确定的实施模式,将调整战略以进一步改善五岁以下儿童的求医情况。 与护理人员和当地社区代表,包括Panchayati Raj Institution (PRI)成员的持续接触,将是完善这些战略的核心。此外,在传播阶段,将与护理人员、社区成员和PRI代表分享主要发现,促进对研究影响的讨论,并为未来的政策和方案决策提供信息。他们的持续参与将有助于对研究结果进行背景分析,并加强旨在改善印度农村肺炎求医行为和有效管理的战略的长期可持续性。
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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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