| Literature DB >> 35103923 |
Bontha V Babu1, Parikipandla Sridevi2, Shaily B Surti3, Manoranjan Ranjit4, Deepa Bhat5, Jatin Sarmah6, Godi Sudhakar7, Yogita Sharma8.
Abstract
This study reports the extent of sickle cell disease (SCD)-related knowledge and management practices of peripheral health workers located in tribal areas of India. This formative qualitative study used a grounded theory approach and collected data through in-depth interviews. It was implemented in six districts endemic to SCD. From each district, four primary health centre (PHC) areas, predominantly inhabited by tribal communities, were included. The participants were 120 peripheral health workers, in two categories-regular health workers (RHWs) and community health workers (CHWs), working in 24 PHCs. Most of the RHWs and a little lesser number of CHWs were aware of SCD, and most of them knew it as a blood disorder. About half of the health workers reported that SCD is hereditary; however, some attributed it to malnutrition and considered it anaemia. Many health workers could tell some typical symptoms of SCD, including anaemia and severe pain. None of the PHCs offered management/treatment of SCD. And none of the health workers has any expertise in managing SCD patients. However, some health workers dealt with SCD cases and provided symptomatic treatment. Though several health workers said that SCD is preventable, comprehensive knowledge on prevention was lacking. Some health workers mentioned mass screening, counselling, and creating awareness. Thus, this paper reports the inadequacy of SCD-related knowledge and management practices among health workers. Health workers should know their roles and capabilities in managing SCD. They should be provided in-service, regular, and structured training programmes as part of the comprehensive SCD programme.Entities:
Keywords: Haemoglobinopathies; Health workers; Knowledge; Qualitative research; Sickle cell disease; Tribal
Year: 2022 PMID: 35103923 PMCID: PMC9270504 DOI: 10.1007/s12687-022-00578-z
Source DB: PubMed Journal: J Community Genet ISSN: 1868-310X