Heath A, Knudsen K
Med Toxicol Adverse Drug Exp. 1987 Jul-Aug;2(4):294-308. doi: 10.1007/BF03259871.
Theophylline, with its narrow therapeutic margin, is a common cause of iatrogenic and deliberate overdose. Most cases of self-poisoning are with sustained release preparations, with peak concentrations occurring up to 12 or more hours after overdose. Toxic symptoms are often seen at concentrations above 15 mg/L. Theophylline is metabolised within the cytochrome P-450 system, with an average total body clearance of 50 to 60 ml/min. Clearance is, however, affected by many factors such as other drugs or disease, and in overdose zero order kinetics may result in prolonged half-lives. Toxicity is characterised by agitation, tremor, nausea, vomiting, abdominal pains, seizures, and tachyarrhythmias. Hypokalaemia and metabolic acidosis are more profound in acute toxicity, and hypercalcaemia is usually present. Seizures occur at lower concentrations after chronic over-medication than after acute overdose. Gastric lavage should be performed in all patients presenting early, and an oral multiple dose charcoal regimen started with 50 to 100g charcoal, repeating with 50g doses and checking theophylline concentrations at 2- to 4-hour intervals. Multiple dose charcoal can be expected to double the clearance of theophylline, being as effective as a haemodialysis. Of the invasive techniques available, charcoal haemoperfusion is the most effective, increasing clearance 4- to 6-fold. Supportive care is particularly important. The aggressive supplementation of potassium, treatment of emesis with droperidol and ranitidine, and treatment of tachyarrhythmias and hypotension (possibly with propranolol), together with oral multiple dose charcoal may obviate the need for haemoperfusion. Seizures suggest increased morbidity and mortality. Charcoal haemoperfusion should be considered if plasma concentrations are greater than 100 mg/L in an acute intoxication or greater than 60 mg/L in a chronic intoxication. The decision to haemoperfuse should not be based on plasma concentrations alone, but an overall evaluation of the patient's laboratory and clinical status.
茶碱治疗窗窄,是医源性和蓄意过量用药的常见原因。大多数自服中毒病例涉及缓释制剂,过量用药后12小时或更长时间出现血药浓度峰值。血药浓度高于15mg/L时常常出现中毒症状。茶碱在细胞色素P-450系统内代谢,平均全身清除率为50至60ml/分钟。然而,清除率受许多因素影响,如其他药物或疾病,过量用药时零级动力学可能导致半衰期延长。中毒的特征为烦躁不安、震颤、恶心、呕吐、腹痛、癫痫发作和快速性心律失常。急性中毒时低钾血症和代谢性酸中毒更严重,通常存在高钙血症。慢性用药过量后癫痫发作的血药浓度低于急性过量用药。所有早期就诊的患者均应进行洗胃,并开始口服多剂量活性炭方案,初始剂量为50至100g活性炭,之后以50g剂量重复给药,并每隔2至4小时检测茶碱浓度。多剂量活性炭有望使茶碱清除率加倍,与血液透析效果相当。在可用的侵入性技术中,活性炭血液灌流最有效,可使清除率提高4至6倍。支持性治疗尤为重要。积极补钾、用氟哌利多和雷尼替丁治疗呕吐、治疗快速性心律失常和低血压(可能用普萘洛尔),以及口服多剂量活性炭可能无需进行血液灌流。癫痫发作提示发病率和死亡率增加。急性中毒时血浆浓度大于100mg/L或慢性中毒时大于60mg/L,应考虑进行活性炭血液灌流。是否进行血液灌流的决定不应仅基于血浆浓度,而应综合评估患者的实验室检查和临床状况。