Khanna Shilpa, Abhishek Shriyuta, Shagill Mohammad, Singh Lakhan, Malik Chetanya, Devi Savithri, Priyadarsh T, Kalkonde Yogeshwar
Sangwari- People's Association for Equity and Health, Surguja, Chhattisgarh, India.
State Health Resource Centre, Raipur, Chhattisgarh, India.
J Family Med Prim Care. 2024 Oct;13(10):4545-4551. doi: 10.4103/jfmpc.jfmpc_382_24. Epub 2024 Oct 18.
The rural-urban healthcare disparity in India was exacerbated during the COVID-19 pandemic, with the second wave hitting rural areas particularly hard due to weak infrastructure. A study in Chhattisgarh aims to explore the experiences of severely ill COVID-19 survivors and caregivers to inform patient-centric care delivery in primary settings.
In this qualitative study, we conducted in-depth interviews with seven patients and seven caregivers during home visits or telephonically to understand lived experiences of receiving care for COVID-19 in an ICU in the public health system. Socioecological model was used to guide the qualitative inquiry.
COVID-19 patients faced stigma due to their diagnosis. The survivors felt lonely due to isolation, uncertainty about their illness, and fear of death. Poor mental health during ICU stay affected their physical health. Patients with caregivers felt supported despite visitor restrictions. Transparent communication with health providers reduced distress.
The study in Chhattisgarh, India, highlights ICU survivors' and caregivers' experiences, revealing fear and loneliness among patients. Effective communication and caregiver presence improve outcomes, emphasizing holistic support. There's an urgent need for palliative care integration, caregiver inclusion, and comprehensive post-discharge follow-up by primary-level practitioners in rural settings. Lack of state-level palliative care policy emphasizes the need for comprehensive initiatives to enhance healthcare outcomes.
在新冠疫情期间,印度城乡医疗差距加剧,由于基础设施薄弱,第二波疫情对农村地区的冲击尤为严重。恰蒂斯加尔邦的一项研究旨在探索重症新冠幸存者及其照顾者的经历,以为基层医疗环境中以患者为中心的护理提供参考。
在这项定性研究中,我们在患者家中或通过电话对7名患者和7名照顾者进行了深入访谈,以了解在公共卫生系统的重症监护病房接受新冠治疗的实际经历。采用社会生态模型指导定性调查。
新冠患者因其诊断结果而面临污名化。幸存者因隔离、对病情的不确定性以及对死亡的恐惧而感到孤独。在重症监护病房住院期间心理健康状况不佳影响了他们的身体健康。有照顾者陪伴的患者尽管存在探视限制,但仍感到得到了支持。与医疗服务提供者的透明沟通减轻了痛苦。
印度恰蒂斯加尔邦的这项研究突出了重症监护病房幸存者及其照顾者的经历,揭示了患者的恐惧和孤独。有效的沟通和照顾者的陪伴可改善治疗效果,强调了全面支持的重要性。农村地区的基层医疗从业者迫切需要整合姑息治疗、纳入照顾者并进行全面的出院后随访。缺乏邦级姑息治疗政策凸显了采取全面举措以改善医疗效果的必要性。