AI Article Synopsis

  • Phenobarbital (PHB) is found to be a safe and effective alternative to benzodiazepines (BZD) for treating severe alcohol withdrawal syndrome (AWS), but its safety in patients previously treated with BZD is unclear.
  • A study compared critically ill patients with severe AWS receiving either PHB or BZD in the ICU to assess outcomes such as resolution of altered mentation, seizures, and length of hospital stay.
  • Results showed no significant difference in the primary outcome between the two groups, but fewer seizures occurred in the PHB group, indicating that PHB may be a viable treatment option after BZD if patients are still experiencing uncontrolled withdrawal.

Article Abstract

Phenobarbital (PHB) is a safe and efficacious alternative to benzodiazepines (BZD) for treating severe alcohol withdrawal (AWS). However, the safety of utilizing PHB for patients initially treated with BZD is unknown. To evaluate the safety and efficacy of PBH compared to BZDs in severe AWS in the medical intensive care unit (ICU). This was a retrospective cohort study comparing critically ill patients admitted for AWS who received BZDs or PHB. The primary outcome was time to persistent resolution of altered mentation. Secondary outcomes included development and duration of delirium, need for mechanical ventilation, development of withdrawal seizures, and ICU and hospital length of stay. Ninety-five patients were evaluated (53 in PHB group, 42 in BZD group). Before study medication, less BZD patients demonstrated abnormal mentation compared with PHB patients (RASS < -2: 2.39% vsvs. 28.12%, respectively, and RASS > +2: 9.9% vsvs. 48.76%; <0.001 for both). No difference was seen between groups for the primary outcome (1.8 hours for BZD cohort vsvs. 13.81 hours for PHB cohort; =0.22). More patients in the BZD cohort developed a seizure after study medication administration (5.67% vs 0%, respectively; =0.02). No significant difference was seen in other secondary outcomes. This study provides support for use of PHB after BZD if patients remain in uncontrolled withdrawal. Despite significant doses of BZDs before PHB, patients in the PHB cohort demonstrated similar clinical and safety outcomes compared to BZD alone.

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Source
http://dx.doi.org/10.1177/08971900241273144DOI Listing

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