Dipyrone overdose

被引:34
作者
Bentur, Y
Cohen, O
机构
[1] Technion Israel Inst Technol, Rambam Med Ctr, Fac Med, Israel Poison Informat Ctr, IL-31096 Haifa, Israel
[2] Ben Gurion Univ Negev, Fac Hlth Sci, Beer Sheva, Israel
来源
JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY | 2004年 / 42卷 / 03期
关键词
dipyrone; agranulocytosis; gastrointestinal; toxicity;
D O I
10.1081/CLT-120037425
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Background: Dipyrone is a pyrazolone derivative used as an analgesic and antipyretic. Agranulocytosis, dipyrone's most serious and potentially fatal adverse effect, has led to its withdrawal in several countries. However, agranulocytosis is subject to geographical variability, ratio with at risks ranging from 0.8-23.7. In many countries dipyrone is still widely used in adults and children and even as an over-the-counter (OTC) preparation. Information on the effects of dipyrone overdose is scanty. Objective: To determine the demographic and clinical characteristics of dipyrone overdose. Methods: Retrospective review of prospectively collected poison center data on acute exposure to dipyrone over a three-year period. The data were subjected to descriptive analysis. Mann-Whitney test and Chi-square analysis were performed where relevant. Results: A total of 243 records met the inclusion and exclusion criteria. Median age was 17 y (4m-83y), median amount 5 g (250 mg-45 g), and median time to consultation was 2 h (5 min-48 h). Toxic events (49) occurred in 39 (16%) patients; 57% of these were gastrointestinal and all were mild. Time to consultation was longer in the symptomatic patients (4 h vs. 1.5 h, respectively, p=0.001) and in children (8 h vs. 3.5 h in adults). Suicidal patients ingested significantly larger amounts (8 g vs. 3.7 g, respectively, p=0.001), as did patients with gastrointestinal symptomatology (7.5 g vs. 5 g in asymptomatics, p=0.001). No agranulocytosis was reported. Discussion: Dipyrone overdose is associated with mild, mainly gastrointestinal toxicity; this was noted at a median dose of 7.5 g. Early gastrointestinal decontamination may have prevented toxicity. The suggested treatment includes gastrointestinal decontamination (if <1 h since ingestion) and supportive measures.
引用
收藏
页码:261 / 265
页数:5
相关论文
共 23 条
[1]   CYCLOOXYGENASE AND LIPOXYGENASE METABOLITE SYNTHESIS BY POLYMORPHONUCLEAR NEUTROPHILS - INVITRO EFFECT OF DIPYRONE [J].
ABBATE, R ;
GORI, AM ;
PINTO, S ;
ATTANASIO, M ;
PANICCIA, R ;
COPPO, M ;
CASTELLANI, S ;
GIUSTI, B ;
BODDI, M ;
SERNERI, GGN .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 1990, 41 (02) :89-93
[2]   PHARMACOKINETICS OF DIPYRONE IN MAN - ROLE OF THE ADMINISTRATION ROUTE [J].
ASMARDI, G ;
JAMALI, F .
EUROPEAN JOURNAL OF DRUG METABOLISM AND PHARMACOKINETICS, 1985, 10 (02) :121-125
[3]   Metamizole use by Latino immigrants: A common and potentially harmful home remedy [J].
Bonkowsky, JL ;
Frazer, JK ;
Buchi, KF ;
Byington, CL .
PEDIATRICS, 2002, 109 (06) :e98
[4]   INFLUENCE OF FOOD ON THE PHARMACOKINETICS OF DIPYRONE [J].
FLUSSER, D ;
ZYLBERKATZ, E ;
GRANIT, L ;
LEVY, M .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1988, 34 (01) :105-107
[5]  
Frolich J C, 1986, Agents Actions Suppl, V19, P155
[6]   HISTORY OF ANTI-PYRETIC ANALGESIC THERAPY [J].
HAAS, H .
AMERICAN JOURNAL OF MEDICINE, 1983, 75 (5A) :1-3
[7]   Agranulocytosis and other blood dyscrasias associated with dipyrone (metamizole) [J].
Hedenmalm, K ;
Spigset, O .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2002, 58 (04) :265-274
[8]  
HUGULEY CM, 1964, JAMA-J AM MED ASSOC, V189, P938
[9]   CLINICAL PHARMACOKINETICS OF DIPYRONE AND ITS METABOLITES [J].
LEVY, M ;
ZYLBERKATZ, E ;
ROSENKRANZ, B .
CLINICAL PHARMACOKINETICS, 1995, 28 (03) :216-234
[10]   PLASMA KINETICS OF DIPYRONE METABOLITES IN RAPID AND SLOW ACETYLATORS [J].
LEVY, M ;
FLUSSER, D ;
ZYLBERKATZ, E ;
GRANIT, L .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1984, 27 (04) :453-458