Toxic alcohol ingestions: Clinical features, diagnosis, and management

被引:256
作者
Krautt, Jeffrey A. [1 ,2 ,3 ]
Kurtztt, Ira [3 ,4 ]
机构
[1] VHAGLA Healthcare Syst, Div Nephrol, Los Angeles, CA 90073 USA
[2] Univ Calif Los Angeles, VHAGLA Healthcare Syst, Membrane Biol Lab, Med & Res Serv, Los Angeles, CA USA
[3] Univ Calif Los Angeles, Ctr Hlth Sci, David Geffen Sch Med, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Ctr Hlth Sci, Div Nephrol, Los Angeles, CA 90024 USA
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2008年 / 3卷 / 01期
关键词
D O I
10.2215/CJN.03220807
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Alcohol-related intoxications, including methanol, ethylene glycol, diethylene glycol, and propylene glycol, and alcoholic ketoacidosis can present with a high anion gap metabolic acidosis and increased serum osmolal gap, whereas isopropanol intoxication presents with hyperosmolality alone. The effects of these substances, except for isopropanol and possibly alcoholic ketoacidosis, are due to their metabolites, which can cause metabolic acidosis and cellular dysfunction. Accumulation of the alcohols in the blood can cause an increment in the osmolality, and accumulation of their metabolites can cause an increase in the anion gap and a decrease in serum bicarbonate concentration. The presence of both laboratory abnormalities concurrently is an important diagnostic clue, although either can be absent, depending on the time after exposure when blood is sampled. In addition to metabolic acidosis, acute renal failure and neurologic disease can occur in some of the intoxications. Dialysis to remove the unmetabolized alcohol and possibly the organic acid anion can be helpful in treatment of several of the alcohol-related intoxications. Administration of fomepizole or ethanol to inhibit alcohol dehydrogenase, a critical enzyme in metabolism of the alcohols, is beneficial in treatment of ethylene glycol and methanol intoxication and possibly diethylene glycol and propylene glycol intoxication. Given the potentially high morbidity and mortality of these intoxications, it is important for the clinician to have a high degree of suspicion for these disorders in cases of high anion gap metabolic acidosis, acute renal failure, or unexplained neurologic disease so that treatment can be initiated early.
引用
收藏
页码:208 / 225
页数:18
相关论文
共 129 条
[1]   Treatment of the alcohol intoxications: ethylene glycol, methanol and isopropanol [J].
Abramson, S ;
Singh, AK .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2000, 9 (06) :695-701
[2]   PLASMA ACID-BASE PATTERNS IN DIABETIC-KETOACIDOSIS [J].
ADROGUE, HJ ;
WILSON, H ;
BOYD, AE ;
SUKI, WN ;
EKNOYAN, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1982, 307 (26) :1603-1610
[3]   Delayed neurologic sequelae resulting from epidemic diethylene glycol poisoning [J].
Alfred, S ;
Coleman, P ;
Harris, D ;
Wigmore, T ;
Stachowski, E ;
Graudins, A .
CLINICAL TOXICOLOGY, 2005, 43 (03) :155-159
[4]  
Almaghamsi AM, 1997, CLIN NEPHROL, V48, P52
[5]   Osmolar gap metabolic acidosis in a 60-year-old man treated for hypoxemic respiratory failure - Propylene glycol toxicity caused by escalating lorazepam infusion. [J].
Arbour, R ;
Esparis, B .
CHEST, 2000, 118 (02) :545-546
[6]  
ARDITI M, 1987, AM J DIS CHILD, V141, P237
[7]   Relationship of continuous infusion lorazepam to serum propylene glycol concentration in critically ill adults [J].
Arroliga, AC ;
Shehab, N ;
McCarthy, K ;
Gonzales, JP .
CRITICAL CARE MEDICINE, 2004, 32 (08) :1709-1714
[8]  
AUZEPY P, 1977, INTENS CARE MED, V3, P196
[9]   Developmental toxicity study with diethylene glycol dosed by gavage to CD rats and CD-1 mice [J].
Ballantyne, B ;
Snellings, WA .
FOOD AND CHEMICAL TOXICOLOGY, 2005, 43 (11) :1637-1646
[10]  
Barceloux DG, 1999, J TOXICOL-CLIN TOXIC, V37, P537