Literature DB >> 21099065

Problematic hospital experiences among adult patients with sickle cell disease.

Lakshmi Lattimer1, Carlton Haywood, Sophie Lanzkron, Neda Ratanawongsa, Shawn M Bediako, Mary Catherine Beach.   

Abstract

BACKGROUND: Adults with sickle cell disease (SCD) have often reported difficulties obtaining care during vaso-occlusive crisis (VOC) in qualitative studies.
METHODS: We measured the experiences of 45 SCD patients who received in-hospital care for VOC using the Picker Patient Experience Questionnaire (PPE-15), and used the one sample binomial test to compare with national norms.
RESULTS: Most SCD patients reported that they were insufficiently involved in decisions (86%), staff gave conflicting information (64%), it wasn't easy to find someone to discuss concerns (61%), doctors' answers to questions were not clear (58%), nurses' answers to questions were not clear (56%), doctors did not always discuss fears and anxieties (53%), and nurses did not always discuss fears and anxieties (52%). A greater percentage of SCD patients than the U.S. sample in 9 of 12 areas reported problems.
CONCLUSIONS: Further research is needed to determine the consequences of and potential interventions to improve these poor experiences.

Entities:  

Mesh:

Year:  2010        PMID: 21099065      PMCID: PMC3240938          DOI: 10.1353/hpu.2010.0940

Source DB:  PubMed          Journal:  J Health Care Poor Underserved        ISSN: 1049-2089


  38 in total

Review 1.  Meta-analysis of correlates of provider behavior in medical encounters.

Authors:  J A Hall; D L Roter; N R Katz
Journal:  Med Care       Date:  1988-07       Impact factor: 2.983

2.  Patients' health as a predictor of physician and patient behavior in medical visits. A synthesis of four studies.

Authors:  J A Hall; D L Roter; M A Milburn; L H Daltroy
Journal:  Med Care       Date:  1996-12       Impact factor: 2.983

3.  Patient race/ethnicity and quality of patient-physician communication during medical visits.

Authors:  Rachel L Johnson; Debra Roter; Neil R Powe; Lisa A Cooper
Journal:  Am J Public Health       Date:  2004-12       Impact factor: 9.308

4.  Evidence suggesting that a chronic disease self-management program can improve health status while reducing hospitalization: a randomized trial.

Authors:  K R Lorig; D S Sobel; A L Stewart; B W Brown; A Bandura; P Ritter; V M Gonzalez; D D Laurent; H R Holman
Journal:  Med Care       Date:  1999-01       Impact factor: 2.983

5.  Communication patterns of primary care physicians.

Authors:  D L Roter; M Stewart; S M Putnam; M Lipkin; W Stiles; T S Inui
Journal:  JAMA       Date:  1997 Jan 22-29       Impact factor: 56.272

6.  Patient and visit characteristics related to physicians' participatory decision-making style. Results from the Medical Outcomes Study.

Authors:  S H Kaplan; B Gandek; S Greenfield; W Rogers; J E Ware
Journal:  Med Care       Date:  1995-12       Impact factor: 2.983

7.  Patients' Perceived Involvement in Care Scale: relationship to attitudes about illness and medical care.

Authors:  C E Lerman; D S Brody; G C Caputo; D G Smith; C G Lazaro; H G Wolfson
Journal:  J Gen Intern Med       Date:  1990 Jan-Feb       Impact factor: 5.128

8.  Pain management and symptoms of substance dependence among patients with sickle cell disease.

Authors:  James Elander; Joanne Lusher; David Bevan; Paul Telfer
Journal:  Soc Sci Med       Date:  2003-11       Impact factor: 4.634

9.  Patient characteristics that influence physician behavior.

Authors:  E M Hooper; L M Comstock; J M Goodwin; J S Goodwin
Journal:  Med Care       Date:  1982-06       Impact factor: 2.983

10.  Experiences of hospital care and treatment-seeking behavior for pain from sickle cell disease: qualitative study.

Authors:  K Maxwell; A Streetly; D Bevan
Journal:  West J Med       Date:  1999-11
View more
  22 in total

1.  Psychometric Properties of the Psychosocial Assessment Tool-General in Adolescents and Young Adults With Sickle Cell Disease.

Authors:  Lori E Crosby; Naomi E Joffe; Nina Reynolds; James L Peugh; Ellen Manegold; Ahna L H Pai
Journal:  J Pediatr Psychol       Date:  2015-08-13

2.  Understanding the Self-Management Practices of Young Adults with Sickle Cell Disease.

Authors:  Nadine Matthie; Coretta Jenerette
Journal:  J Sick Cell Dis Hemoglobinopathies       Date:  2017-05

3.  Depressive symptoms and sickle cell pain: The moderating role of internalized stigma.

Authors:  Breanna M Holloway; Lakeya S McGill; Shawn M Bediako
Journal:  Stigma Health       Date:  2017-11

4.  A Qualitative Study of Chronic Pain and Self-Management in Adults with Sickle Cell Disease.

Authors:  Nadine Matthie; Diana Ross; Cynthia Sinha; Kirshma Khemani; Nitya Bakshi; Lakshmanan Krishnamurti
Journal:  J Natl Med Assoc       Date:  2018-09-26       Impact factor: 1.798

5.  Family Engagement in Pediatric Sickle Cell Disease Visits.

Authors:  Elizabeth D Cox; Matthew P Swedlund; Henry N Young; Megan A Moreno; Jennifer M Schopp; Victoria Rajamanickam; Julie A Panepinto
Journal:  Health Commun       Date:  2016-05-09

6.  Perceptions of young adults with sickle cell disease concerning their disease experience.

Authors:  Nadine Matthie; Jill Hamilton; Diana Wells; Coretta Jenerette
Journal:  J Adv Nurs       Date:  2015-09-09       Impact factor: 3.187

7.  An unequal burden: poor patient-provider communication and sickle cell disease.

Authors:  Carlton Haywood; Shawn Bediako; Sophie Lanzkron; Marie Diener-West; John Strouse; Jennifer Haythornthwaite; Gladys Onojobi; Mary Catherine Beach
Journal:  Patient Educ Couns       Date:  2014-05-23

8.  Care seeking for pain in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl A Brewer; Kenneth I Ataga
Journal:  Pain Manag Nurs       Date:  2013-01-21       Impact factor: 1.929

9.  Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease.

Authors:  Carlton Haywood; Marie Diener-West; John Strouse; C Patrick Carroll; Shawn Bediako; Sophie Lanzkron; Jennifer Haythornthwaite; Gladys Onojobi; Mary Catherine Beach
Journal:  J Pain Symptom Manage       Date:  2014-04-15       Impact factor: 3.612

10.  Patient Safety Events and Harms During Medical and Surgical Hospitalizations for Persons With Serious Mental Illness.

Authors:  Gail L Daumit; Emma E McGinty; Peter Pronovost; Lisa B Dixon; Eliseo Guallar; Daniel E Ford; Elizabeth K Cahoon; Romsai T Boonyasai; David Thompson
Journal:  Psychiatr Serv       Date:  2016-05-16       Impact factor: 3.084

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.