Intravenous dolasetron for the prevention of postoperative nausea and vomiting after outpatient laparoscopic gynecologic surgery

被引:65
作者
Graczyk, SG
McKenzie, R
Kallar, S
Hickok, CB
Melson, T
Morrill, B
Hahne, WF
Brown, RA
机构
[1] MAGEE WOMENS HOSP, PITTSBURGH, PA USA
[2] VIRGINIA COMMONWEALTH UNIV, MED COLL VIRGINIA, RICHMOND, VA 23298 USA
[3] GEORGE WASHINGTON UNIV, MED CTR, WASHINGTON, DC 20037 USA
[4] HELEN KELLER HOSP, MUSCLE SHOALS, AL USA
[5] HOECHST MARION ROUSSEL, KANSAS CITY, MO USA
关键词
D O I
10.1097/00000539-199702000-00015
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The newer 5-hydroxytryptamine type 3 (5-HT3) antagonists are sometimes considered for routine prophylaxis of postoperative nausea and vomiting (PONV) in high-risk patients. This multicenter, randomized, double-blind, placebo-controlled study compared the efficacy and safety of three single intravenous (IV) doses of dolasetron mesylate salt (12.5, 25, or 50 mg) for the prevention of PONV in 635 females undergoing outpatient laparoscopic gynecologic surgery. Antiemetic efficacy was evaluated over a 24-h postoperative period by recording the number and timing of emetic episodes; effects on nausea were evaluated by a visual analog scale (VAS). The proportion of complete responders (no emetic episodes and no escape medication in 24 h) was significantly higher with each dolasetron mesylate dose (> 50% for each dose; P less than or equal to 0.0003) than with placebo (30.6%). Fewer patients given dolasetron required or requested escape antiemetic medication compared with placebo (P < 0.0003). Dolasetron-treated patients had significantly (P < 0.0357) lower median postdose maximum nausea VAS scores compared with placebo-treated patients. Patient satisfaction with dolasetron was high and, overall, was significantly (P = 0.0131) greater than that with placebo. Dolasetron was an effective and well tolerated preventive treatment for PONV resulting from laparoscopic gynecologic surgery.
引用
收藏
页码:325 / 330
页数:6
相关论文
共 23 条
[1]   5-HT3 RECEPTOR ANTAGONISTS - AN OVERVIEW OF THEIR PRESENT STATUS AND FUTURE POTENTIAL IN CANCER THERAPY-INDUCED EMESIS [J].
AAPRO, MS .
DRUGS, 1991, 42 (04) :551-568
[2]  
Audhuy B, 1996, EUR J CANCER, V32A, P807
[3]  
CAMU F, 1992, EUR J ANAESTH, P25
[4]   ACUTE ANTIEMETIC EFFICACY AND SAFETY OF DOLASETRON MESYLATE, A 5-HT3 ANTAGONISTS, IN CANCER-PATIENTS TREATED WITH CISPLATIN [J].
CONROY, T ;
CAPPELAERE, P ;
FABBRO, M ;
FAUSER, AA ;
SPLINTER, TAW ;
SPIELMANN, M ;
SCHNEIDER, M ;
CHEVALLIER, B ;
GOUPIL, A ;
CHAUVERGNE, J ;
FARGEOT, P ;
PREVOT, G ;
OGRADY, P ;
GREEN, D ;
HARDENBERG, J ;
BOYCE, M .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 1994, 17 (02) :97-102
[5]   ORAL ONDANSETRON FOR PREVENTING NAUSEA AND VOMITING [J].
COOKE, CE ;
MEHRA, IV .
AMERICAN JOURNAL OF HOSPITAL PHARMACY, 1994, 51 (06) :762-771
[6]   REDUCING CHEMOTHERAPY-INDUCED NAUSEA AND VOMITING - CURRENT PERSPECTIVES AND FUTURE POSSIBILITIES [J].
DELFAVERO, A ;
ROILA, F ;
TONATO, M .
DRUG SAFETY, 1993, 9 (06) :410-428
[7]   THE EFFECT OF ORAL ONDANSETRON IN THE PREVENTION OF POSTOPERATIVE NAUSEA AND VOMITING AFTER MAJOR GYNECOLOGICAL SURGERY PERFORMED UNDER GENERAL-ANESTHESIA [J].
DUPEYRON, JP ;
CONSEILLER, C ;
LEVARLET, M ;
HEMMINGSEN, C ;
SCHOEFFLER, P ;
PEDERSEN, FM ;
GRIBOMONT, B ;
KAPLAN, LA .
ANAESTHESIA, 1993, 48 (03) :214-218
[8]  
Galvan Martin, 1993, Drugs of the Future, V18, P506
[9]  
HELMERS JH, 1992, EUROPEAN J ANAEST S6, V9, P49
[10]   Double-blind, randomized comparison of the antiemetic efficacy of intravenous dolasetron mesylate and intravenous ondansetron in the prevention of acute cisplatin-induced emesis in patients with cancer [J].
Hesketh, P ;
Navari, R ;
Grote, T ;
Gralla, R ;
Hainsworth, J ;
Kris, M ;
Anthony, L ;
Khojasteh, A ;
Tapazoglou, E ;
Benedict, C ;
Hahne, W .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (08) :2242-2249