TY - JOUR
T1 - Improved Smoking Cessation Rates in a Pharmacist-Led Program Embedded in an Inflammatory Bowel Disease Specialty Medical Home
AU - Tse, Stacy Saithy
AU - Sands, Bruce E.
AU - Keefer, Laurie
AU - Cohen, Benjamin L.
AU - Maser, Elana
AU - Ungaro, Ryan C.
AU - Marion, James F.
AU - Colombel, Jean Frédéric
AU - Itzkowitz, Steven H.
AU - Gelman, Jessica
AU - Dubinsky, Marla C.
N1 - Funding Information:
The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: Bruce E. Sands reports consulting or speaking for the following: AbbVie, Arena Pharmaceuticals, AstraZeneca, Boehringer Ingelheim, Boston Pharmaceuticals, Capella Bioscience, Celltrion Healthcare, Genentech, Gilead, Hoffmann-La Roche, Ironwood Pharmaceuticals, Janssen, Lilly, Morphic Therapeutic, Oppilan Pharma, Otsuka, Pfizer, Prometheus Laboratories, Shire, Takeda, TARGET PharmaSolutions, Theravance Biopharma, Vivelix Pharmaceuticals. Reports researching support from Theravance Biopharma. Laurie Keefer: Research funding from Abbvie. Consultant for Pfizer. Board of Directors, Rome Foundation, Co-Founder Trellus Health. Benjamin L. Cohen: Participates in advisory boards and consulting for Abbvie, Allergan, Janssen, Target PharmaSolutions, and Sublimity Therapeutics. Ryan C. Ungaro: Consultant for Takeda, Pfizer, and Janssen and has received research support from AbbVie, Boehringer Ingelheim, and Pfizer. Supported by an NIH K23 Career Development Award (K23KD111995-01A1) and Career Development Award from the Crohn’s and Colitis Foundation. Jean-Frédéric Colombel: Reports receiving research grants from AbbVie, Janssen Pharmaceuticals and Takeda; receiving payment for lectures from AbbVie, Amgen, Allergan, Inc. Ferring Pharmaceuticals, Shire, and Takeda; receiving consulting fees from AbbVie, Amgen, Arena Pharmaceuticals, Boehringer Ingelheim, Celgene Corporation, Celltrion, Eli Lilly, Enterome, Ferring Pharmaceuticals, Genentech, Janssen Pharmaceuticals, Landos, Ipsen, Medimmune, Merck, Novartis, Pfizer, Shire, Takeda, Tigenix, Viela bio; and hold stock options in Intestinal Biotech Development and Genfit. Steven H. Itzkowitz: Consultant for Exact Sciences Corporation. Marla C. Dubinsky: Consultant for Prometheus Labs, Janssen, Abbvie, Takeda, Pfizer, Celgene, Arena, Genentech, Lilly, Boehringer Ingelheim.
Publisher Copyright:
© The Author(s) 2021.
PY - 2022/12
Y1 - 2022/12
N2 - Background: Cigarette smoking is associated with disease progression, poor outcomes, and increased biologic use in Crohn’s Disease (CD). In this prospective study, we describe the structure and results of a pharmacist-driven smoking cessation program in an Inflammatory Bowel Disease (IBD) Specialty Medical Home. Methods: One pharmacist designed and implemented a collaborative drug therapy management (CDTM) program, which allowed the pharmacist to initiate and modify smoking cessation aids, monitor medication safety and efficacy, and provide behavioral counseling. Crohn’s Disease patients who were current smokers and referred to the program were analyzed. Clinical and demographic data, disease activity, and smoking history were collected. The primary outcome was the proportion of patients in the enrolled group and the declined group who quit smoking at least once during the follow-up period. Secondary outcomes include demographic and clinical differences between enrolled and declined patients, and enrolled quitters and non-quitters. Results: Thirty-two patients were referred to the program and 19 participated. Over a median follow-up period of 305 [264-499] days, 42% (8/19) of enrolled patients quit smoking at least once. Fifteen percent (2/13) of declined patients quit smoking. Patients who continued to smoke had more instances of loss of response to a biologic, need to start a new biologic, or escalation of biologic therapy. The CDTM pharmacist was able to provide all necessary clinical services for smokers enrolled in the program. Conclusions: A pharmacist-led smoking cessation program in a specialty medical home is feasible. It may result in successful quit attempts and may optimize IBD medication use.
AB - Background: Cigarette smoking is associated with disease progression, poor outcomes, and increased biologic use in Crohn’s Disease (CD). In this prospective study, we describe the structure and results of a pharmacist-driven smoking cessation program in an Inflammatory Bowel Disease (IBD) Specialty Medical Home. Methods: One pharmacist designed and implemented a collaborative drug therapy management (CDTM) program, which allowed the pharmacist to initiate and modify smoking cessation aids, monitor medication safety and efficacy, and provide behavioral counseling. Crohn’s Disease patients who were current smokers and referred to the program were analyzed. Clinical and demographic data, disease activity, and smoking history were collected. The primary outcome was the proportion of patients in the enrolled group and the declined group who quit smoking at least once during the follow-up period. Secondary outcomes include demographic and clinical differences between enrolled and declined patients, and enrolled quitters and non-quitters. Results: Thirty-two patients were referred to the program and 19 participated. Over a median follow-up period of 305 [264-499] days, 42% (8/19) of enrolled patients quit smoking at least once. Fifteen percent (2/13) of declined patients quit smoking. Patients who continued to smoke had more instances of loss of response to a biologic, need to start a new biologic, or escalation of biologic therapy. The CDTM pharmacist was able to provide all necessary clinical services for smokers enrolled in the program. Conclusions: A pharmacist-led smoking cessation program in a specialty medical home is feasible. It may result in successful quit attempts and may optimize IBD medication use.
KW - inflammatory bowel disease
KW - medical home
KW - pharmacist
KW - smoking cessation
UR - http://www.scopus.com/inward/record.url?scp=85104049413&partnerID=8YFLogxK
U2 - 10.1177/08971900211000682
DO - 10.1177/08971900211000682
M3 - Article
C2 - 33827316
AN - SCOPUS:85104049413
SN - 0897-1900
VL - 35
SP - 827
EP - 835
JO - Journal of Pharmacy Practice
JF - Journal of Pharmacy Practice
IS - 6
ER -