Diazepam/lorazepam/propylene glycol

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Reactions 1083 - 7 Jan 2006 24 hours. S Wilson KC, et al. Propylene glycol toxicity: a severe iatrogenic illness in ICU Diazepam/lorazepam/propylene glycol patients receiving IV benzodiazepines: a case series and prospective, observational pilot study. Chest 128: 1674-1681, No. 3, Sep 2005 - USA 800992470 Metabolic disorders associated with propylene glycol toxicity: 9 case reports Six men and three women developed metabolic disorders associated with propylene glycol toxicity while receiving propylene glycol-containing IV diazepam or IV lorazepam infusions for sedation during ventilation or alcohol withdrawal [see table for patient details]. Patient characteristics and treatment details Patient Age Drug/total dose Duration Total (years)/ of propylene Sex treatment glycol (days) dose (g) 1 48/M Lorazepam 7 444 1070mg 2 61/M Diazepam 5 970 4850mg 3 41/M Lorazepam 11g 25 4565 4 30/F Lorazepam 9 1273 3068mg 5 53/M Lorazepam 7 899 2166mg 6 34/M Diazepam 20mg 2 306 Lorazepam 730mg 7 60/F Diazepam 290mg 3 511 Lorazepam 1092mg 8 35/F Lorazepam 68mg 2 28 9 35/M Diazepam 2 490 2450mg Patient 1’s anion gap and creatinine level increased on treatment days 6 and 7, and his serum bicarbonate level and pH decreased. Despite treatment with antibacterials, his metabolic disorders continued to worsen. Lorazepam was switched to midazolam and his metabolic parameters normalised within 24 hours. Patient 2’s anion gap increased on day 6, and his serum bicarbonate level and pH decreased. Diazepam was switched to midazolam and his metabolic disorders resolved within 24 hours. Patient 3’s anion gap and creatinine level increased on day 23 and he developed hypotension. His metabolic disorders worsened over the next 2 days. Lorazepam was switched to midazolam and his metabolic disorders improved over the next 24 hours. Patient 4’s anion gap increased over the first 3 days and she developed acute renal failure. Her metabolic disorders worsened over the next 6 days despite initiation of haemodialysis and antibacterial therapy. Lorazepam was discontinued and her metabolic parameters and renal function normalised within 24 hours. Patient 5’s serum bicarbonate level decreased and his creatinine level increased during the lorazepam infusion. Lorazepam was discontinued and his metabolic disorders resolved within 72 hours. Patient 6’s bicarbonate level decreased progressively over 3 days. Lorazepam and diazepam were switched to midazolam and his metabolic parameters normalised within 24 hours. Patient 7’s bicarbonate level decreased on day 4, and diazepam and lorazepam were switched to midazolam. Her metabolic parameters normalised within 48 hours. Patient 8’s anion gap increased on day 3, and lorazepam was switched to midazolam. Her metabolic disorder resolved within 24 hours. Patient 9’s bicarbonate level decreased progressively over 3 days and her anion gap increased. Diazepam was switched to midazolam and her metabolic disorders resolved within 1 Reactions 7 Jan 2006 No. 1083 0114-9954/10/1083-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

Transcript of Diazepam/lorazepam/propylene glycol

Page 1: Diazepam/lorazepam/propylene glycol

Reactions 1083 - 7 Jan 2006

24 hours. S Wilson KC, et al. Propylene glycol toxicity: a severe iatrogenic illness in ICUDiazepam/lorazepam/propylene glycol

patients receiving IV benzodiazepines: a case series and prospective, observationalpilot study. Chest 128: 1674-1681, No. 3, Sep 2005 - USA 800992470Metabolic disorders associated with propylene

glycol toxicity: 9 case reportsSix men and three women developed metabolic disorders

associated with propylene glycol toxicity while receivingpropylene glycol-containing IV diazepam or IV lorazepaminfusions for sedation during ventilation or alcohol withdrawal[see table for patient details].

Patient characteristics and treatment detailsPatient Age Drug/total dose Duration Total

(years)/ of propyleneSex treatment glycol

(days) dose (g)

1 48/M Lorazepam 7 4441070mg

2 61/M Diazepam 5 9704850mg

3 41/M Lorazepam 11g 25 45654 30/F Lorazepam 9 1273

3068mg5 53/M Lorazepam 7 899

2166mg6 34/M Diazepam 20mg 2 306

Lorazepam730mg

7 60/F Diazepam 290mg 3 511 Lorazepam

1092mg8 35/F Lorazepam 68mg 2 289 35/M Diazepam 2 490

2450mg

Patient 1’s anion gap and creatinine level increased ontreatment days 6 and 7, and his serum bicarbonate level andpH decreased. Despite treatment with antibacterials, hismetabolic disorders continued to worsen. Lorazepam wasswitched to midazolam and his metabolic parametersnormalised within 24 hours.

Patient 2’s anion gap increased on day 6, and his serumbicarbonate level and pH decreased. Diazepam was switchedto midazolam and his metabolic disorders resolved within24 hours.

Patient 3’s anion gap and creatinine level increased onday 23 and he developed hypotension. His metabolicdisorders worsened over the next 2 days. Lorazepam wasswitched to midazolam and his metabolic disorders improvedover the next 24 hours.

Patient 4’s anion gap increased over the first 3 days and shedeveloped acute renal failure. Her metabolic disordersworsened over the next 6 days despite initiation ofhaemodialysis and antibacterial therapy. Lorazepam wasdiscontinued and her metabolic parameters and renal functionnormalised within 24 hours.

Patient 5’s serum bicarbonate level decreased and hiscreatinine level increased during the lorazepam infusion.Lorazepam was discontinued and his metabolic disordersresolved within 72 hours.

Patient 6’s bicarbonate level decreased progressively over3 days. Lorazepam and diazepam were switched to midazolamand his metabolic parameters normalised within 24 hours.

Patient 7’s bicarbonate level decreased on day 4, anddiazepam and lorazepam were switched to midazolam. Hermetabolic parameters normalised within 48 hours.

Patient 8’s anion gap increased on day 3, and lorazepam wasswitched to midazolam. Her metabolic disorder resolvedwithin 24 hours.

Patient 9’s bicarbonate level decreased progressively over3 days and her anion gap increased. Diazepam was switchedto midazolam and her metabolic disorders resolved within

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Reactions 7 Jan 2006 No. 10830114-9954/10/1083-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved