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Randomized Controlled Trial
A randomized double-blind placebo-controlled study of low-dose intravenous Lorazepam to reduce procedural pain during bone marrow aspiration and biopsy.
- Se Hoon Park, Soo-Mee Bang, Eunmi Nam, Eun Kyung Cho, Dong Bok Shin, Jae Hoon Lee, and Jeong Yeal Ahn.
- Department of Internal Medicine, Gachon University Gil Medical Center, Incheon, Korea.
- Pain Med. 2008 Mar 1;9(2):249-52.
ObjectiveTo evaluate the efficacy of intravenous lorazepam as premedication for bone marrow aspiration and biopsy (BMAB).DesignRandomized, double-blind, placebo-controlled.PatientsOne hundred and thirty-eight consenting patients planned to receive BMAB.InterventionPatients were randomly assigned to receive either intravenous lorazepam 1 mg or placebo just prior to BMAB.SettingTertiary referral center, inpatient setting.Outcome MeasuresA questionnaire was used to determine the patient perception about the procedure and pain at baseline, which was completed just after the procedure, and the next day after the BMAB. Pain was rated using a 10-cm linear visual analog scale (VAS).ResultsThe mean VAS scores measured during the BMAB examination were 6.0 for lorazepam vs 6.2 for placebo. Few adverse events were noted during intravenous lorazepam administration. The patients in the lorazepam group were more likely to accept the next BMAB (P = 0.044).ConclusionIntravenous lorazepam was safe in patients undergoing BMAB and was more effective than placebo in enhancing cooperation during BMAB and willingness to undergo another procedure. However, use of lorazepam 1 mg provided no reduction in the pain associated with BMAB. Further studies should focus on providing appropriate analgesia for this potentially painful procedure.
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