Converting adults with sickle cell disease from full agonist opioids to buprenorphine: A reliable method with safety and early evidence of reduced acute care utilization-Reference-Cited by-同舟云学术

Converting adults with sickle cell disease from full agonist opioids to buprenorphine: A reliable method with safety and early evidence of reduced acute care utilization

Published:2022-09-14 Issue:11 Volume:97 Page:1435-1442
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:American J Hematol

Author:

David Mandy S.¹^ORCID,Jones Jennifer¹,Lauriello Ashley¹,Nnake Ijeoma¹,Plazas Montana Manuela¹,Lasko Kyra²,Buri‐Nagua Carlos³,Olagbaju Yetunde¹,Williams Elizabeth¹,Sears Matthew¹,Salzberg Benjamin⁴,Lanzkron Sophie M.¹,Carroll C. Patrick⁵

Affiliation:

1. Department of Medicine, Division of Hematology The Johns Hopkins University School of Medicine Baltimore Maryland USA

2. Department of Emergency Medicine University of Maryland Medical System Baltimore Maryland USA

3. Johns Hopkins University, Homewood Campus Baltimore Maryland USA

4. University of Maryland College Park Maryland USA

5. Department of Psychiatry and Behavioral Sciences The Johns Hopkins School of Medicine Baltimore Maryland USA

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.26699

Reference39 articles.

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2. Medical care utilization and mortality in sickle cell disease: A population-based study

3. Mortality Rates and Age at Death from Sickle Cell Disease: U.S., 1979–2005

4. Hematologic Problems in Psychosomatic Medicine

5. HassellK.Sickle cell disease population estimation: application of available contemporary data to traditional methods. Paper presented at: 35th Anniversary Convention of the National Sickle Cell Disease Program and the Sickle Cell Disease Association of America;2007.

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