Babu Bontha V, Sridevi Parikipandla, Surti Shaily B, Bhat Deepa, Sarmah Jatin, Sudhakar Godi, Sharma Yogita
Division of Socio-Behavioural & Health Systems Research, Indian Council of Medical Research, New Delhi, 110 029, India.
Department of Biotechnology, Indira Gandhi National Tribal University, Amarkantak, India.
J Community Genet. 2022 Dec;13(6):597-603. doi: 10.1007/s12687-022-00614-y. Epub 2022 Oct 13.
Sickle cell disease (SCD) is a progressively debilitating genetic disease, and India is the second most affected nation in the prevalence of births with SCD. This SCD prevalence is high among Indian indigenous tribal communities, whose healthcare is pluralistic. Traditional healers are an essential part of tribal pluralistic care. This study aimed to understand the extent of SCD-related knowledge and practices of traditional healers and their willingness to participate in the SCD programme, which is primarily meant to screen and treat SCD. Following the grounded theory approach, data were collected by in-depth interviews with 40 traditional healers selected from five SCD endemic districts. Text data were coded through a deductive approach, and thematic content analysis was carried out. A few healers knew about SCD. However, almost all are aware of anaemia and its symptoms. Most healers were unaware of the cause of SCD and mentioned that malnutrition and anaemia are reasons for the recurrence of SCD-related symptoms. Most of the traditional healers did not give any treatment. Some gave symptomatic treatment and provided herbal medicines along with some rituals. Though some healers treated some of the typical symptoms of SCD like spleen enlargement, jaundice, swelling and pains in joints, they did not link them with SCD. All traditional healers expressed concern and said they support the government-run SCD programme. The programme should recognise the role and importance of traditional healers. Necessary education on SCD may be given to the healers. Such involvement and education empower the healers in appropriately guiding the people concerning SCD care.
镰状细胞病(SCD)是一种逐渐使人衰弱的遗传疾病,在出生时患有SCD的患病率方面,印度是受影响第二严重的国家。这种SCD患病率在印度本土部落社区中很高,这些社区的医疗保健是多元化的。传统治疗师是部落多元化护理的重要组成部分。本研究旨在了解传统治疗师对SCD相关知识和实践的程度,以及他们参与主要用于筛查和治疗SCD的SCD项目的意愿。遵循扎根理论方法,通过对从五个SCD流行地区挑选的40名传统治疗师进行深入访谈来收集数据。文本数据通过演绎方法进行编码,并进行了主题内容分析。一些治疗师了解SCD。然而,几乎所有人都知道贫血及其症状。大多数治疗师不知道SCD的病因,并提到营养不良和贫血是SCD相关症状复发的原因。大多数传统治疗师没有进行任何治疗。一些人进行了对症治疗,并提供草药以及一些仪式。尽管一些治疗师治疗了SCD的一些典型症状,如脾脏肿大、黄疸、关节肿胀和疼痛,但他们没有将这些症状与SCD联系起来。所有传统治疗师都表示关注,并表示他们支持政府开展的SCD项目。该项目应认识到传统治疗师的作用和重要性。可以向治疗师提供关于SCD的必要教育。这种参与和教育使治疗师能够在SCD护理方面适当地指导人们。