Development of a Pipeline for Removing Allergy Labels in Patients Undergoing Hematopoietic Stem Cell Transplantation.


Journal

Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629

Informations de publication

Date de publication:
Mar 2024
Historique:
received: 16 10 2023
revised: 07 12 2023
accepted: 15 12 2023
medline: 18 3 2024
pubmed: 23 12 2023
entrez: 22 12 2023
Statut: ppublish

Résumé

Penicillin allergy is reported by 10% to 20 % of patients, but when evaluated only 1% to 2% may have a true allergy. Patients undergoing hematopoietic stem cell transplantation (HSCT) have a high likelihood of requiring beta-lactam antibiotics due to increased infection risk, which can be limited by a penicillin allergy label. When a penicillin allergy is recorded, alternatives are needed, including more expensive broader-spectrum antibiotics, with increases in drug-resistant bacteria, longer hospital stays, higher expenditures, and increases in nosocomial infections, such as Clostridium difficile colitis. This group of patients already undergoes extensive pretreatment testing and would especially benefit from allergy delabeling. This study aimed to develop a self-sustaining, low-cost pipeline between an HSCT clinic and an allergy clinic to identify and successfully delabel low-risk patients who endorse an allergy to penicillin, amoxicillin, amoxicillin-clavulanate, piperacillin-tazobactam, or ampicillin before admission to the hospital. We developed a survey to triage allergy risk, identified key stakeholders in building the pipeline, and underwent 4 plan, do, study, act (PDSA) cycles. Changes were made in each of the PDSA cycles to minimize cost and uncompensated provider time, as well as to increase patient retention throughout the pipeline by increasing appointment availability and decreasing reliance on patients to independently progress through the pathway. Of the 410 patients with planned HSCT who were screened over 11 months, 89 (21.7%) were listed as having a penicillin and/or beta lactam allergy. All but 1 (66 of 67; 98.5%) of the participants completed the survey accurately when confirmed by an allergist, and the survey was 100% accurate in predicting delabeling success in low-risk patients. Of eligible patients, 43.8% (n = 39) were successfully delabeled before their transplant date, and 97.4% of these (n = 38) have undergone HSCT to date. This pipeline is maintained by approximately 5 hours of work per week (1 hour of allergy physician time, 4 hours of nurse and/or clinical coordinator time), with no other direct costs. There is an estimated direct savings of at least $1914.93 per patient delabeled. We successfully designed and implemented a pipeline between the HSCT clinic and the allergy clinic as a quality improvement initiative to identify and address high rates of reported beta-lactam allergies. We identified and addressed patient-based factors, logistical, temporal, and financial barriers that impacted patient retention and sustainability. This model is expected to yield significant and sustained cost savings for the healthcare system as well as to improve patient outcomes, and this hypothesis is currently undergoing formal analysis. We anticipate that this model can be used to create a similar pipeline in other healthcare systems for HSCT recipients, as well as patients in other clinical settings, such as oncology and chimeric antigen receptor T cell therapy.

Identifiants

pubmed: 38134971
pii: S2666-6367(23)01747-5
doi: 10.1016/j.jtct.2023.12.012
pii:
doi:

Substances chimiques

Penicillins 0
Amoxicillin 804826J2HU
beta-Lactams 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

322.e1-322.e10

Informations de copyright

Copyright © 2023 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Lauren E Merz (LE)

Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

George X Huang (GX)

Division of Allergy and Immunology, Brigham and Women's Hospital, Boston, Massachusetts.

Geneva D Mehta (GD)

Division of Allergy and Immunology, Brigham and Women's Hospital, Boston, Massachusetts.

Donna-Marie Lynch (DM)

Division of Allergy and Immunology, Brigham and Women's Hospital, Boston, Massachusetts.

Natalia Maliborski (N)

Center for Clinical Investigation, Brigham and Women's Hospital, Boston, Massachusetts.

Kylie Besz (K)

Division of Allergy and Immunology, Brigham and Women's Hospital, Boston, Massachusetts.

Paige Wickner (P)

Division of Allergy and Immunology, Brigham and Women's Hospital, Boston, Massachusetts.

Corey Cutler (C)

Division of Transplantation and Cellular Therapy, Dana-Farber Cancer Institute, Boston, Massachusetts.

Mariana Castells (M)

Division of Allergy and Immunology, Brigham and Women's Hospital, Boston, Massachusetts. Electronic address: mcastells@bwh.harvard.edu.

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Classifications MeSH