Literature DB >> 21190745

Structure and process measures of quality of care in adult congenital heart disease patients: a pan-Canadian study.

Luc M Beauchesne1, Judith Therrien, Nanette Alvarez, Lynn Bergin, Gary Burggraf, Philippe Chetaille, Elaine Gordon, Catherine M Kells, Marla Kiess, Lise-Andrée Mercier, Erwin N Oechslin, Jeffrey Stein, James W Tam, Dylan Taylor, Anne Williams, Paul Khairy, Andrew S Mackie, Candice K Silversides, Ariane J Marelli.   

Abstract

BACKGROUND: There are more adults than children with congenital heart disease. Of over 96,000 ACHD patients in Canada, approximately 50% require ongoing expert care. In spite of published recommendations, data on the quality of care for ACHD patients are lacking.
METHODS: Survey methodology targeted all Canadian Adult Congenital Heart (CACH) network affiliated ACHD centers. Clinics were asked to prospectively collect outpatient and procedural volumes for 2007. In 2008, centers were surveyed regarding infrastructure, staffing, patient volumes and waiting times.
RESULTS: All 15 CACH network registered centers responded. The total number of patients followed in ACHD clinics was 21,879 (median per clinic=1132 (IQR: 585, 1816)). Of the total 80 adult and pediatric cardiologists affiliated to an ACHD clinic, only 27% had received formal ACHD training. Waiting times for non-urgent consultations were 4 ± 2 months, and 4 ± 3 months for percutaneous and surgical procedures. These were beyond Canadian recommended targets at 11 sites (73%) for non-urgent consultations, at 8 sites (53%) for percutaneous interventions and 13 sites (87%) for surgery.
CONCLUSIONS: Of a minimum number of 96,000 ACHD patients in Canada, only 21,879 were being regularly followed in 2007. At most sites waiting times for ACHD services were beyond Canadian recommended targets. In spite of universal health care access, published guidelines for ACHD patient structure and process measures of health care quality are not being met.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 21190745     DOI: 10.1016/j.ijcard.2010.12.024

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  10 in total

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Review 2.  Transition of Care in Congenital Heart Disease: Ensuring the Proper Handoff.

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Review 3.  From adolescents to adults with congenital heart disease: the role of transition.

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Review 5.  So hard to say goodbye: transition from paediatric to adult cardiology care.

Authors:  Adrienne H Kovacs; Brian W McCrindle
Journal:  Nat Rev Cardiol       Date:  2013-11-12       Impact factor: 32.419

6.  Psychological Distress in Adults With Congenital Heart Disease Over the COVID-19 Pandemic.

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7.  Association of Adult Congenital Heart Disease With Pregnancy, Maternal, and Neonatal Outcomes.

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Journal:  JAMA Netw Open       Date:  2019-05-03

8.  A cluster randomized trial of a transition intervention for adolescents with congenital heart disease: rationale and design of the CHAPTER 2 study.

Authors:  Andrew S Mackie; Gwen R Rempel; Adrienne H Kovacs; Miriam Kaufman; Kathryn N Rankin; Ahlexxi Jelen; Cedric Manlhiot; Samantha J Anthony; Joyce Magill-Evans; David Nicholas; Renee Sananes; Erwin Oechslin; Dimi Dragieva; Sonila Mustafa; Elina Williams; Michelle Schuh; Brian W McCrindle
Journal:  BMC Cardiovasc Disord       Date:  2016-06-06       Impact factor: 2.298

9.  A welcome to the new journal, International Journal of Cardiology - Heart and Vessels (IJC-H + V).

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Journal:  Int J Cardiol Heart Vessel       Date:  2013-11-14

10.  Global, regional, and national time trends in mortality for congenital heart disease, 1990-2019: An age-period-cohort analysis for the Global Burden of Disease 2019 study.

Authors:  Zhanhao Su; Zhiyong Zou; Simon I Hay; Yiwei Liu; Shoujun Li; Huiwen Chen; Mohsen Naghavi; Meghan S Zimmerman; Gerard R Martin; Lauren B Wilner; Craig A Sable; Christopher J L Murray; Nicholas J Kassebaum; George C Patton; Hao Zhang
Journal:  EClinicalMedicine       Date:  2022-01-11
  10 in total

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