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Increased Risk of New-Onset Hypertension in Patients With Narcolepsy Initiating Sodium Oxybate: A Real-World Study.
Ben-Joseph, Rami H; Somers, Virend K; Black, Jed; D'Agostino, Ralph B; Davis, Mat; Macfadden, Wayne; Mues, Katherine E; Jackson, Clark; Ni, Weiyi; Cook, Michael N; White, William B.
Afiliação
  • Ben-Joseph RH; Jazz Pharmaceuticals, Inc, Palo Alto, CA. Electronic address: Rami@h-e-o-r.com.
  • Somers VK; Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN.
  • Black J; Jazz Pharmaceuticals, Inc, Palo Alto, CA; Stanford University Center for Sleep Sciences and Medicine, Department of Psychiatry and Behavioral Sciences, Palo Alto, CA.
  • D'Agostino RB; Wake Forest University School of Medicine, Winston-Salem, NC.
  • Davis M; Jazz Pharmaceuticals, Inc, Philadelphia, PA.
  • Macfadden W; Jazz Pharmaceuticals, Inc, Philadelphia, PA.
  • Mues KE; Aetion, Inc, New York, NY.
  • Jackson C; Aetion, Inc, New York, NY.
  • Ni W; Jazz Pharmaceuticals, Inc, Palo Alto, CA.
  • Cook MN; Jazz Pharmaceuticals, Inc, Philadelphia, PA.
  • White WB; Pat and Jim Calhoun Cardiology Center, University of Connecticut, Farmington, CT.
Mayo Clin Proc ; 2024 Aug 22.
Article em En | MEDLINE | ID: mdl-39177543
ABSTRACT

OBJECTIVE:

To compare intermediate-term risk of new-onset hypertension between normotensive patients with narcolepsy initiating sodium oxybate (SXB cohort) and those not initiating sodium oxybate (control cohort). PATIENTS AND

METHODS:

This retrospective cohort study used MarketScan administrative claims data from January 1, 2014, to February 29, 2020. Eligible patients were 18 years of age or older with continuous enrollment (≥180 days before and after cohort entry), had one or more narcolepsy claims or a prescription fill for sodium oxybate, had no history of hypertension or antihypertensive medication use, and had no use of sodium oxybate within 13 months before cohort entry. Patients in the SXB and control cohorts were matched 12 for the propensity score to balance baseline characteristics. End points were (1) a composite of new-onset hypertension diagnosis or antihypertensive medication initiation and (2) new-onset hypertension diagnosis. Patients were monitored for 180 days, until outcome occurrence, sodium oxybate discontinuation (SXB cohort), or sodium oxybate initiation (control cohort). Risk per 100 patients was reported; differences were evaluated using logistic regression to estimate adjusted odds ratios (ORs) and 95% confidence intervals (CIs).

RESULTS:

The SXB and control cohorts included 954 and 1908 patients, respectively. Risk of new-onset hypertension diagnosis or antihypertensive medication initiation was higher in the SXB cohort than in the control cohort (6.60 vs 4.20 per 100 patients; OR, 1.61; 95% CI, 1.15 to 2.27). Risk of a new-onset hypertension diagnosis only in the SXB cohort was 0.94 per 100 patients and 0.52 per 100 patients in the control cohort (OR, 1.81; 95% CI, 0.73 to 4.46).

CONCLUSION:

In this study, sodium oxybate use was associated with a new-onset hypertension diagnosis or antihypertensive medication initiation in normotensive patients with narcolepsy.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article