Literature DB >> 19851232

Feed forward systems for patient participation and provider support: adoption results from the original US context to Sweden and beyond.

Helena Hvitfeldt1, Cheryl Carli, Eugene C Nelson, Dawne M Mortenson, Birgit A Ruppert, Staffan Lindblad.   

Abstract

BACKGROUND: This is a study of 2 clinical feed forward systems (FFSs) situated in different contexts: in the United States, where the system was developed, and in Swedish clinical settings, where it was first adopted. Both systems were identified as clinically successful despite differing contexts, and the objective of this study is to understand what essential properties determined their success.
METHODS: In our search for essential properties of the FFS, we used acceptance, use, and utility as indicators in questionnaires and interviews of patients and providers. Properties were identified as essential if they enabled reinforcing loops favorable for patients, providers, or both at clinical encounters.
RESULTS: A total of 44 patients participated in each context, along with 13 providers from the United States and 6 providers from the Swedish clinics. In the patient questionnaire, a majority of patients rated their impression of the FFS as excellent to good (United States: 84%, Sweden: 96%, P < .001). Interviews with both patients and providers indicated that the FFS patient overview displaying structured data previous to the clinical encounter is favorable. These essential properties enabled patient involvement through engagement, education, and communication with the provider, who appreciated them as time-saving for managing data and as decision support. DISCUSSION: Despite distinctly different contexts and locally adapted content, essential properties that induced successful patient participation and provider support were identified as universal in the FFSs. Thus, further spread of the FFS may be enabled to accomplish patient-centered care and improved clinical information and quality management.

Entities:  

Mesh:

Year:  2009        PMID: 19851232     DOI: 10.1097/QMH.0b013e3181bee32e

Source DB:  PubMed          Journal:  Qual Manag Health Care        ISSN: 1063-8628            Impact factor:   0.926


  13 in total

1.  Framework for assessing quality of care for inflammatory bowel disease in Sweden.

Authors:  Martin Rejler; Jörgen Tholstrup; Mattias Elg; Anna Spångéus; Boel Andersson Gäre
Journal:  World J Gastroenterol       Date:  2012-03-14       Impact factor: 5.742

2.  Validation of the Patient-Reported Outcomes Measurement Information System (PROMIS)-57 and -29 item short forms among kidney transplant recipients.

Authors:  Evan Tang; Oladapo Ekundayo; John Devin Peipert; Nathaniel Edwards; Aarushi Bansal; Candice Richardson; Susan J Bartlett; Doris Howell; Madeline Li; David Cella; Marta Novak; Istvan Mucsi
Journal:  Qual Life Res       Date:  2018-11-22       Impact factor: 4.147

Review 3.  The impact of patient-reported outcome measures in clinical practice for pain: a systematic review.

Authors:  Michelle M Holmes; George Lewith; David Newell; Jonathan Field; Felicity L Bishop
Journal:  Qual Life Res       Date:  2016-11-04       Impact factor: 4.147

4.  Chiropractors' views on the use of patient-reported outcome measures in clinical practice: a qualitative study.

Authors:  Michelle M Holmes; Felicity L Bishop; David Newell; Jonathan Field; George Lewith
Journal:  Chiropr Man Therap       Date:  2018-12-18

5.  Can practitioners use patient reported measures to enhance person centred coordinated care in practice? A qualitative study.

Authors:  Hannah Wheat; Jane Horrell; Jose M Valderas; James Close; Ben Fosh; Helen Lloyd
Journal:  Health Qual Life Outcomes       Date:  2018-12-04       Impact factor: 3.186

6.  Empowering Young People Living With Juvenile Idiopathic Arthritis to Better Communicate With Families and Care Teams: Content Analysis of Semistructured Interviews.

Authors:  Meghan R Longacre; Stuart W Grande; Karin Palmblad; Meera V Montan; Rikard P Berquist; Andreas Hager; Greg Kotzbauer
Journal:  JMIR Mhealth Uhealth       Date:  2019-02-22       Impact factor: 4.773

7.  Sharing Patient-Controlled Real-World Data Through the Application of the Theory of Commons: Action Research Case Study.

Authors:  Andreas Hager; Staffan Lindblad; Mats Brommels; Stina Salomonsson; Carolina Wannheden
Journal:  J Med Internet Res       Date:  2021-01-19       Impact factor: 5.428

8.  Learning health systems using data to drive healthcare improvement and impact: a systematic review.

Authors:  Joanne Enticott; Alison Johnson; Helena Teede
Journal:  BMC Health Serv Res       Date:  2021-03-05       Impact factor: 2.655

Review 9.  Patient-Reported Outcomes in Patients with Chronic Kidney Disease and Kidney Transplant-Part 1.

Authors:  Evan Tang; Aarushi Bansal; Marta Novak; Istvan Mucsi
Journal:  Front Med (Lausanne)       Date:  2018-01-15

10.  Leaders' perspectives on learning health systems: a qualitative study.

Authors:  Joanne Enticott; Sandra Braaf; Alison Johnson; Angela Jones; Helena J Teede
Journal:  BMC Health Serv Res       Date:  2020-11-26       Impact factor: 2.655

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.