Public reporting: accountability or witch-hunt?

2008 ◽  
Vol 90 (6) ◽  
pp. 194-196
Author(s):  
Elaine Towell

As demand for greater public accountability and transparency in the UK health care system continues to grow, surgeons of all specialties are in discussion on how best to produce outcome data specific to individual clinicians. In the US individual outcomes for cardiac surgery have been published in some states for almost 20 years, yet surgeons here and abroad remain sceptical as to whether the benefits of public reporting outweigh the negatives.

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Sugy Choi ◽  
Heesu Shin ◽  
Jongho Heo ◽  
Etsegenet Gedlu ◽  
Berhanu Nega ◽  
...  

Abstract Background Surgery can correct congenital heart defects, but disease management in low- and middle-income countries can be challenging and complex due to a lack of referral system, financial resources, human resources, and infrastructure for surgical and post-operative care. This study investigates the experiences of caregivers of children with CHD accessing the health care system and pediatric cardiac surgery. Methods A qualitative study was conducted at a teaching hospital in Ethiopia. We conducted semi-structured interviews with 13 caregivers of 10 patients with CHD who underwent cardiac surgery. We additionally conducted chart reviews for triangulation and verification. Interviews were conducted in Amharic and then translated into English. Data were analyzed according to the principles of interpretive thematic analysis, informed by the candidacy framework. Results The following four observations emerged from the interviews: (a) most patients were diagnosed with CHD at birth if they were born at a health care facility, but for those born at home, CHD was discovered much later (b) many patients experienced misdiagnoses before seeking care at a large hospital, (c) after diagnosis, patients were waiting for the surgery for more than a year, (d) caregivers felt anxious and optimistic once they were able to schedule the surgical date. During the care-seeking journey, caregivers encountered financial constraints, struggled in a fragmented delivery system, and experienced poor service quality. Conclusions Delayed access to care was largely due to the lack of early CHD recognition and financial hardships, related to the inefficient and disorganized health care system. Fee waivers were available to assist low-income children in gaining access to health services or medications, but application information was not readily available. Indirect costs like long-distance travel contributed to this challenge. Overall, improvements must be made for district-level screening and the health care workforce.


JAMA ◽  
2019 ◽  
Vol 322 (15) ◽  
pp. 1501 ◽  
Author(s):  
William H. Shrank ◽  
Teresa L. Rogstad ◽  
Natasha Parekh

2018 ◽  
pp. 38-54
Author(s):  
John Fry ◽  
Donald Light ◽  
Jonathan Rodnick ◽  
Peter Orton

2003 ◽  
Vol 6 (6) ◽  
pp. 720-721
Author(s):  
I Girod ◽  
F Pang ◽  
A Saleh ◽  
J Edington

2018 ◽  
Vol 7 (1) ◽  
pp. 15-28 ◽  
Author(s):  
Grace Hampson ◽  
Adrian Towse ◽  
Steven D Pearson ◽  
William B Dreitlein ◽  
Chris Henshall

2012 ◽  
Vol 25 (1) ◽  
pp. 74-76 ◽  
Author(s):  
David A. Klein ◽  
Ginny Gildengorin ◽  
Peter Mosher ◽  
William P. Adelman

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