Scharman Elizabeth J, Erdman Andrew R, Wax Paul M, Chyka Peter A, Caravati E Martin, Nelson Lewis S, Manoguerra Anthony S, Christianson Gwenn, Olson Kent R, Woolf Alan D, Keyes Daniel C, Booze Lisa L, Troutman William G
American Association of Poison Control Centers, Washington, DC 20016, USA.
Clin Toxicol (Phila). 2006;44(3):205-23. doi: 10.1080/15563650600585920.
In 2003, there were 28,092 human exposures to diphenhydramine reported to poison centers in the US. A related drug, dimenhydrinate, is a less frequent cause of poisonings. Between January 2000 and June 2004, there were 2,534 reported dimenhydrinate ingestions in children less than 6 years of age. An evidence-based expert consensus process was used to create this guideline. Relevant articles were abstracted by a trained physician researcher. The first draft was created by the primary author. The entire panel discussed and refined the guideline before distribution to secondary reviewers for comment. The panel then made changes based on the secondary review comments. The objective of this guideline is to assist poison center personnel in the appropriate out-of-hospital triage and initial management of patients with a suspected ingestion of diphenhydramine or dimenhydrinate, or a dermal exposure to diphenhydramine. This guideline is based on an assessment of current scientific and clinical information. The expert consensus panel recognizes that specific patient care decisions may be at variance with this guideline and are the prerogative of the patient and the health professionals providing care, considering all of the circumstances involved. This guideline does not substitute for clinical judgment. The panel's recommendations for dermal or oral exposures to diphenhydramine or oral exposures to dimenhydrinate follow. The grade of recommendation is in parentheses: 1) All patients with suicidal intent, intentional abuse, or in cases in which a malicious intent is suspected (e.g., child abuse or neglect) should be referred to an emergency department (Grade D). 2) In patients without evidence of self-harm, abuse, or malicious intent, poison center personnel should elicit additional information including the time of the ingestion or dermal exposure, determination of the precise dose ingested, and the presence of co-ingestants (Grade D). 3) Patients experiencing any changes in behavior other than mild drowsiness or mild stimulation should be referred to an emergency department. Examples of moderate to severe symptoms that warrant referral include agitation, staring spells, inconsolable crying, hallucinations, abnormal muscle movements, loss of consciousness, seizures, or respiratory depression (Grade D). 4) For patients referred to the emergency department, transportation via ambulance should be considered based on several factors including the condition of the patient and the length of time it will take the patient to arrive at the emergency department (Grade D). 5) If the patient has no symptoms, and more than 4 hours have elapsed between the time of diphenhydramine ingestion and the call to the poison center, referral to an emergency department is not recommended. For dermal exposures to diphenhydramine, if the patient has no symptoms and it has been more than 8 hours since the diphenhydramine was thoroughly removed from the skin, referral to an emergency department is not recommended (Grade D). 6) Patients with acute ingestions of less than a toxic dose of diphenhydramine, or chronic exposures to diphenhydramine and no or mild symptoms, can be observed at home with instructions to call the poison center back if symptoms develop or worsen. The poison center should consider making a follow-up call at approximately 4 hours after ingestion (Grade D). 7) Children less than 6 years of age who ingest at least 7.5 mg/kg of diphenhydramine should be referred to an emergency department (Grade D). 8) Patients 6 years of age and older who ingest at least 7.5 mg/kg or 300 mg of diphenhydramine (whichever is less), should be referred to an emergency department (Grade D). 9) If the patient has no symptoms, and more than 6 hours have elapsed between the time of dimenhydrinate ingestion and the call to the poison center, referral to an emergency department is not recommended (Grade D). 10) Patients with acute ingestions of less than a toxic dose of dimenhydrinate, or chronic exposures to dimenhydrinate and no or mild symptoms, can be observed at home with instructions to call the poison center back if symptoms develop or worsen. The poison center should consider making a follow-up call at approximately 6 hours after ingestion (Grade D). 11) Children less than 6 years of age ingesting at least 7.5 mg/kg of dimenhydrinate should be referred to an emergency department (Grade D). 12) Patients 6 years of age and older ingesting at least 7.5 mg/kg or 300 mg of dimenhydrinate (whichever is less), should be referred to an emergency department for evaluation (Grade D). 13) Following oral exposures of diphenhydramine or dimenhydrinate, do not induce emesis. Because of the potential for diphenhydramine or dimenhydrinate to cause loss of consciousness or seizures, activated charcoal should not be administered en route to an emergency department (Grade D). 14) For chronic dermal exposures of diphenhydramine, skin decontamination (with water or soap and water) should be attempted prior to transporting a patient to an emergency department unless moderate to severe symptoms are already present. In this circumstance, transportation should not be delayed, and EMS personnel should attempt skin decontamination en route to the emergency department (Grade D). 15) Intravenous sodium bicarbonate may be administered by EMS personnel if QRS widening (QRS >0.10 msec) is present and if authorized by EMS medical direction (Grade D). 16) Physostigmine should be reserved for administration in a hospital (Grade D). 17) Benzodiazepines may be administered by EMS personnel if agitation or seizures are present, and if authorized by EMS medical direction (Grade D).
2003年,美国毒物控制中心接到28,092例人体接触苯海拉明的报告。一种相关药物茶苯海明,是中毒事件较少见的诱因。2000年1月至2004年6月期间,有2534例6岁以下儿童摄入茶苯海明的报告。本指南是通过循证专家共识程序制定的。相关文章由一名经过培训的医师研究人员提取摘要。初稿由第一作者撰写。整个专家组在将指南分发给二级评审人员征求意见之前,对其进行了讨论和完善。然后,专家组根据二级评审意见进行了修改。本指南的目的是协助毒物控制中心人员对疑似摄入苯海拉明或茶苯海明或皮肤接触苯海拉明的患者进行适当的院外分诊和初始处理。本指南基于对当前科学和临床信息的评估。专家共识小组认识到,特定的患者护理决策可能与本指南不一致,在考虑所有相关情况后,这是患者和提供护理的卫生专业人员的特权。本指南不能替代临床判断。专家组针对皮肤或口服接触苯海拉明或口服接触茶苯海明的建议如下。推荐等级在括号内:1) 所有有自杀意图、故意滥用药物或怀疑有恶意意图的患者(如虐待或忽视儿童)应转诊至急诊科(D级)。2) 对于没有自我伤害、滥用药物或恶意意图证据的患者,毒物控制中心人员应获取更多信息,包括摄入或皮肤接触的时间、确定准确的摄入剂量以及是否存在合并摄入物(D级)。3) 除轻度嗜睡或轻度兴奋外,出现任何行为改变的患者应转诊至急诊科。需要转诊的中度至重度症状的例子包括烦躁不安、凝视发作、无法安抚的哭闹、幻觉、异常肌肉运动、意识丧失、癫痫发作或呼吸抑制(D级)。4) 对于转诊至急诊科的患者,应根据包括患者状况以及患者到达急诊科所需时间等多个因素考虑通过救护车转运(D级)。5) 如果患者没有症状,且从摄入苯海拉明到致电毒物控制中心已过去4小时以上,则不建议转诊至急诊科。对于皮肤接触苯海拉明的情况,如果患者没有症状且苯海拉明从皮肤上彻底清除后已过去8小时以上,则不建议转诊至急诊科(D级)。6) 急性摄入苯海拉明剂量低于中毒剂量或慢性接触苯海拉明且无或仅有轻度症状的患者,可以在家中观察,并告知如果症状出现或加重应回拨毒物控制中心电话。毒物控制中心应考虑在摄入后约4小时进行随访电话(D级)。7) 摄入至少7.5 mg/kg苯海拉明的6岁以下儿童应转诊至急诊科(D级)。8) 摄入至少7.5 mg/kg或300 mg苯海拉明(以较低者为准)的6岁及以上患者,应转诊至急诊科进行评估(D级)。9) 如果患者没有症状,且从摄入茶苯海明到致电毒物控制中心已过去6小时以上,则不建议转诊至急诊科(D级)。10) 急性摄入茶苯海明剂量低于中毒剂量或慢性接触茶苯海明且无或仅有轻度症状的患者,可以在家中观察,并告知如果症状出现或加重应回拨毒物控制中心电话。毒物控制中心应考虑在摄入后约6小时进行随访电话(D级)。11) 摄入至少7.5 mg/kg茶苯海明的6岁以下儿童应转诊至急诊科(D级)。12) 摄入至少7.5 mg/kg或300 mg茶苯海明(以较低者为准)的6岁及以上患者,应转诊至急诊科进行评估(D级)。13) 口服接触苯海拉明或茶苯海明后,不要催吐。由于苯海拉明或茶苯海明有可能导致意识丧失或癫痫发作,在转运至急诊科途中不应给予活性炭(D级)。14) 对于苯海拉明的慢性皮肤接触,在将患者转运至急诊科之前,应尝试进行皮肤去污(用水或肥皂水),除非已经出现中度至重度症状。在这种情况下,不应延迟转运,急救医疗服务人员应在转运至急诊科途中尝试进行皮肤去污(D级)。15) 如果出现QRS增宽(QRS>0.10毫秒)且经急救医疗服务医疗指导授权,急救医疗服务人员可给予静脉注射碳酸氢钠(D级)。16) 毒扁豆碱应保留在医院使用(D级)。17) 如果出现烦躁不安或癫痫发作且经急救医疗服务医疗指导授权,急救医疗服务人员可给予苯二氮䓬类药物(D级)。