1995
DOI: 10.1016/0885-3924(95)00104-7
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Reduction of nausea and vomiting from epidural opioids by adding droperidol to the infusate in home-bound patients

Abstract: In 184 adult patients with severe nonmalignant low back pain from postlaminectomy syndrome, temporary lumbar epidural catheters were infused with either 0.25% bupivacaine 92 mL, fentanyl 600 micrograms, and droperidol 5 mg (Group A), or 0.25% bupivacaine 92 mL, fentanyl 600 micrograms, and NaCl 0.9% 2 mL (Group B). Infusion rates ranged from 0.5 to 2 mL per hour, with an option for turning the infusion off when the patient had no pain and turning it on when the pain returned. Infusions were continued from 2 to… Show more

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Cited by 20 publications
(8 citation statements)
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“…From the clinician's perspective, it is important to identify the underlying cause of nausea and vomiting from among the multiple causative mechanisms for each patient so that effective treatment can be chosen (Table 1). Opioid stimulation of the CTZ leading to nausea and vomiting can be treated with dopamine receptor antagonists such as phenothiazines (e.g., prochlorperazine) or butyrophenones (e.g., haloperidol and droperidol), though dopamine antagonism with these agents can cause a range of side effects such as drowsiness, constipation, dystonia, parkinsonism, tardive dyskinesia, torsades de pointes, and neuroleptic malignant syndrome [20,42,43]. Serotonin receptor antagonists (e.g., dolasetron, granisetron, and ondansetron) are also effective for the prevention of nausea and vomiting caused by opioid stimulation of the CTZ, and are associated with a good tolerability profile [17,20].…”
Section: Implications For Clinicians and Patientsmentioning
confidence: 99%
“…From the clinician's perspective, it is important to identify the underlying cause of nausea and vomiting from among the multiple causative mechanisms for each patient so that effective treatment can be chosen (Table 1). Opioid stimulation of the CTZ leading to nausea and vomiting can be treated with dopamine receptor antagonists such as phenothiazines (e.g., prochlorperazine) or butyrophenones (e.g., haloperidol and droperidol), though dopamine antagonism with these agents can cause a range of side effects such as drowsiness, constipation, dystonia, parkinsonism, tardive dyskinesia, torsades de pointes, and neuroleptic malignant syndrome [20,42,43]. Serotonin receptor antagonists (e.g., dolasetron, granisetron, and ondansetron) are also effective for the prevention of nausea and vomiting caused by opioid stimulation of the CTZ, and are associated with a good tolerability profile [17,20].…”
Section: Implications For Clinicians and Patientsmentioning
confidence: 99%
“…Previous experience in non-malignant patients with severe low back pain demonstrated that adding 5 mg of droperidol to epidural bupivacaine-fentanyl mixture was efficacious in reducing the incidence of these gastrointestinal symptoms [1]. The mechanism of these actions could involve agonist activity at the spinal and supraspinal levels and also dopamine antagonism.…”
Section: Spinal Route and Use Of Spinal Adjuvantsmentioning
confidence: 97%
“…Side effects, including drowsiness, constipation, dystonia, and parkinsonism, are largely dose dependent. 6,10,24 Tardive dyskinesia, torsades de pointes, and neuroleptic malignant syndrome are other adverse effects that may occur with butyrophenones and are considered to be dose independent.…”
Section: Treatmentmentioning
confidence: 99%
“…4 In a study of 260 patients with cancer pain receiving opioids, nausea was rated as moderate to severe in 8. [3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18].3%, regardless of the drug. This suggests that patients receiving palliative care frequently experience nausea and constipation, and opioids contribute significantly to these symptoms.…”
mentioning
confidence: 99%
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