Literature DB >> 25639822

Impact of a dedicated infusion clinic for acute management of adults with sickle cell pain crisis.

Sophie Lanzkron1, C Patrick Carroll, Peter Hill, Mandy David, Nicklaine Paul, Carlton Haywood.   

Abstract

Most adults with sickle cell disease (SCD) receive care for their acute painful episodes in an emergency department (ED) setting. The purpose of this article is to describe the impact of opening a dedicated treatment center for adults with SCD [Sickle Cell Infusion Clinic (SCIC)] on patient outcomes and on hospital discharges for SCD. Descriptive data including demographics, time to first dose of narcotic, and pain scores were collected on patients presenting to the SCIC and ED. Maryland hospital discharge data were obtained from the Maryland Health Services Cost Review Commission. Analyses were conducted using T tests, χ(2) tests, and simple generalized estimating equation regression models accounting for the clustered nature of observations, as appropriate. There were 3,874 visits to the SCIC by 361 unique patients; 85% of those visits resulted in the patient being sent home. During the same time period, there were 3,408 visits to the ED by 558 unique patients with SCD. The overall admission rate from the ED for these patients was 35.9% but decreased significantly over the time period with a rate of 20% in December 2011. There was a significant decrease in readmissions over time for the entire Baltimore Metro area with the likelihood of readmission decreasing by 7% over time. The SCIC model provides adults with SCD access to high quality care that decreases the need for hospital admission. Further research needs to be done to evaluate the cost effectiveness of this model.
© 2015 Wiley Periodicals, Inc.

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Year:  2015        PMID: 25639822      PMCID: PMC4409504          DOI: 10.1002/ajh.23961

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  16 in total

1.  Day case management of sickle pain: 3 years experience in a UK sickle cell unit.

Authors:  J Wright; D Bareford; C Wright; G Augustine; K Olley; L Musamadi; C Dhanda; C Knight
Journal:  Br J Haematol       Date:  2004-09       Impact factor: 6.998

2.  Effectiveness of a dedicated day hospital for management of acute sickle cell pain.

Authors:  Adeboye H Adewoye; Vikki Nolan; Lillian McMahon; Qianli Ma; Martin H Steinberg
Journal:  Haematologica       Date:  2007-06       Impact factor: 9.941

Review 3.  A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease.

Authors:  Carlton Haywood; Mary Catherine Beach; Sophie Lanzkron; John J Strouse; Renee Wilson; Haeseong Park; Catherine Witkop; Eric B Bass; Jodi B Segal
Journal:  J Natl Med Assoc       Date:  2009-10       Impact factor: 1.798

4.  Painful crises in sickle cell disease--patients' perspectives.

Authors:  N Murray; A May
Journal:  BMJ       Date:  1988-08-13

5.  The management of sickle cell crisis pain as experienced by patients and their carers.

Authors:  J Alleyne; V J Thomas
Journal:  J Adv Nurs       Date:  1994-04       Impact factor: 3.187

6.  Sickle cell anemia day hospital: an approach for the management of uncomplicated painful crises.

Authors:  L J Benjamin; G I Swinson; R L Nagel
Journal:  Blood       Date:  2000-02-15       Impact factor: 22.113

7.  Treatment of uncomplicated vaso-occlusive crises in children with sickle cell disease in a day hospital.

Authors:  Jean L Raphael; Aditi Kamdar; M Brooke Beavers; Donald H Mahoney; Brigitta U Mueller
Journal:  Pediatr Blood Cancer       Date:  2008-07       Impact factor: 3.167

8.  Mortality in sickle cell disease. Life expectancy and risk factors for early death.

Authors:  O S Platt; D J Brambilla; W F Rosse; P F Milner; O Castro; M H Steinberg; P P Klug
Journal:  N Engl J Med       Date:  1994-06-09       Impact factor: 91.245

Review 9.  Models of comprehensive multidisciplinary care for individuals in the United States with genetic disorders.

Authors:  Scott D Grosse; Michael S Schechter; Roshni Kulkarni; Michele A Lloyd-Puryear; Bonnie Strickland; Edwin Trevathan
Journal:  Pediatrics       Date:  2009-01       Impact factor: 7.124

10.  Day hospital versus inpatient management of uncomplicated vaso-occlusive crises in children with sickle cell disease.

Authors:  Jean L Raphael; Aditi Kamdar; Tao Wang; Hao Liu; Donald H Mahoney; Brigitta U Mueller
Journal:  Pediatr Blood Cancer       Date:  2008-09       Impact factor: 3.167

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  12 in total

1.  American Society of Hematology 2020 guidelines for sickle cell disease: management of acute and chronic pain.

Authors:  Amanda M Brandow; C Patrick Carroll; Susan Creary; Ronisha Edwards-Elliott; Jeffrey Glassberg; Robert W Hurley; Abdullah Kutlar; Mohamed Seisa; Jennifer Stinson; John J Strouse; Fouza Yusuf; William Zempsky; Eddy Lang
Journal:  Blood Adv       Date:  2020-06-23

2.  Communalism Moderates the Association Between Racial Centrality and Emergency Department Use for Sickle Cell Disease Pain.

Authors:  Shawn M Bediako; Chey Harris
Journal:  J Black Psychol       Date:  2017-03-01

3.  Synthesis and evaluation of resveratrol derivatives as fetal hemoglobin inducers.

Authors:  Priscila Longhin Bosquesi; Aylime Castanho Bolognesi Melchior; Aline Renata Pavan; Carolina Lanaro; Cristiane Maria de Souza; Radda Rusinova; Rafael Consolin Chelucci; Karina Pereira Barbieri; Guilherme Felipe Dos Santos Fernandes; Iracilda Zepone Carlos; Olaf Sparre Andersen; Fernando Ferreira Costa; Jean Leandro Dos Santos
Journal:  Bioorg Chem       Date:  2020-05-16       Impact factor: 5.275

4.  Optimal disease management and health monitoring in adults with sickle cell disease.

Authors:  Jo Howard; Swee Lay Thein
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

5.  Increased acute care utilization in a prospective cohort of adults with sickle cell disease.

Authors:  Sophie Lanzkron; Jane Little; Joshua Field; Joseph Ryan Shows; Hang Wang; Rebecca Seufert; Jasmine Brooks; Ravi Varadhan; Carlton Haywood; Mustapha Saheed; Chiung Yu Huang; Brandi Griffin; Steven Frymark; Allie Piehet; Derek Robertson; Marc Proudford; Adrienne Kincaid; Charles Green; Lorri Burgess; Marcus Wallace; Jodi Segal
Journal:  Blood Adv       Date:  2018-09-25

6.  Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects.

Authors:  Julie Kanter; Wally R Smith; Payal C Desai; Marsha Treadwell; Biree Andemariam; Jane Little; Diane Nugent; Susan Claster; Deepa G Manwani; Judith Baker; John J Strouse; Ifeyinwa Osunkwo; Rosalyn W Stewart; Allison King; Lisa M Shook; John D Roberts; Sophie Lanzkron
Journal:  Blood Adv       Date:  2020-08-25

7.  Emergency Department (ED), ED Observation, Day Hospital, and Hospital Admissions for Adults with Sickle Cell Disease.

Authors:  David M Cline; Susan Silva; Caroline E Freiermuth; Victoria Thornton; Paula Tanabe
Journal:  West J Emerg Med       Date:  2018-02-12

8.  Young Adult Perspectives on a Successful Transition from Pediatric to Adult Care in Sickle Cell Disease.

Authors:  Amy E Sobota; Emeka Umeh; Jennifer W Mack
Journal:  J Hematol Res       Date:  2015-12

9.  Barriers and facilitators to care for individuals with sickle cell disease in central North Carolina: The emergency department providers' perspective.

Authors:  Rita Vanessa Masese; Dominique Bulgin; Christian Douglas; Nirmish Shah; Paula Tanabe
Journal:  PLoS One       Date:  2019-05-07       Impact factor: 3.240

10.  Letter to the Editor: Physicians' Opinions of COVID-19 Ambulatory Care Constraints: A Survey of Sickle Cell Clinicians.

Authors:  Martha O Kenney; Benjamin Becerra; Sean Alexander Beatty; Wally Smith
Journal:  J Ambul Care Manage       Date:  2021 Oct-Dec 01
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