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1.
PLoS One ; 14(8): e0220316, 2019.
Article in English | MEDLINE | ID: mdl-31369610

ABSTRACT

INTRODUCTION: The National Rural Health Mission (NRHM) was launched in India in 2005 to address the health needs of under-served populations in rural areas, and to support universal access to care. Despite this initiative, unaccredited informal providers (IPs) often remain patients' first point of contact, which has led to inconsistencies in treatment, and has compromised the quality of care. AIM: To explore the factors that influence patients' decisions about healthcare providers in rural areas of central India. METHODS: Nine focus group discussions (FGDs) were held in nine villages in central India. Framework analysis using an inductive approach was used to analyse the data. RESULTS: The crosscutting theme across the discussions was not choice but need-the need for affordable and accessible health care regardless of the provider's qualification. Results highlighted that IPs play a pivotal role in villagers' lives. Formal healthcare services were accessed infrequently, and mainly when a condition was judged severe or possibly even fatal. Even then, affordability was carefully weighed. Villagers' distance from formal providers contributed to high cost and low preference of formal providers. When opting for IPs, familiarity and trust were more important to villagers than qualifications. IPs have operated in rural communities in India for a long time and have adapted their services to meet the needs, preferences, social norms, and economic conditions of villagers. CONCLUSION: IPs have captured a niche and are often the first contact point in rural settings even when patients ultimately are diagnosed and treated by trained doctors. Merely tackling the undersupply of qualified doctors is not effective or sufficient to impact on the rural healthcare system: the strong and prevalent influence of IPs needs to be addressed also.


Subject(s)
Patient Acceptance of Health Care/psychology , Adolescent , Adult , Aged , Choice Behavior , Developing Countries , Female , Focus Groups , Health Services Accessibility , Humans , India , Male , Middle Aged , Poverty , Rural Population , Young Adult
2.
J Surg Res ; 205(1): 252-259.e1, 2016 09.
Article in English | MEDLINE | ID: mdl-27329569

ABSTRACT

BACKGROUND: A total of 17,000 patients receive kidney transplants each year in the United States. The 30-day readmission rate for kidney transplant recipients is over 30%. Our research focuses on the relationship between the quality of care delivered during the patient's hospital stay for a kidney transplant, and the patient health outcomes and readmissions related to the transplant. METHODS: We interviewed 20 kidney transplant recipients at a major transplant center in the United States. Findings from these interviews were used to inform the data collection using structured surveys, which were administered to an additional 77 kidney transplant recipients. We used ordinary least squares regression to predict the effects of two dimensions of in-hospital care quality-information consistency and empathetic care delivery-on level of patient anxiety 1 week following discharge. Further, we estimated a logistic regression to predict the effect of anxiety, combined with the two dimensions of in-hospital care quality, on occurrence of 30-day readmissions. RESULTS: Patient anxiety levels 1 wk after discharge are significantly associated with information consistency and empathetic delivery of care. Patient anxiety 1 wk after discharge is associated with occurrence of 30-d readmissions. The logistic regression model indicates that the risk of getting readmitted is 110% higher for a one unit increase in patient anxiety level 1 wk after discharge. Finally, patient anxiety fully mediates the effects of consistency of information and empathetic care delivery on occurrence of 30-d readmissions (50.96% of the effect is mediated). CONCLUSIONS: Our study suggests two ways of preventing readmissions through reduction of postdischarge anxiety: (1) standardizing in-hospital care, so that information received by patients is consistent, and (2) by training caregivers to be more empathetic toward patients during the delivery of this information.


Subject(s)
Anxiety/prevention & control , Kidney Transplantation/psychology , Patient Readmission/statistics & numerical data , Quality of Health Care , Adolescent , Adult , Aged , Female , Humans , Interviews as Topic , Male , Middle Aged , Reproducibility of Results , Surveys and Questionnaires , Young Adult
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