Ayling John
Buncombe County EMS, Asheville, NC, USA.
Emerg Med Serv. 2003 May;32(5):48.
This was a great save. The crew could easily have missed the presentation of anaphylaxis and let the window for treatment with epinephrine slip away. This patient was in anaphylactic shock. There were no signs that supported a traumatic injury, and that, combined with diaphoresis, urticaria and tachycardic central pulse, contributed to the suspicion of anaphylaxis. Anaphylaxis is classified as distributive shock. This type of shock is caused by profound systemic vasodilation, and the heart is unable to increase output enough to maintain blood pressure. Other causes of distributive shock include sepsis and spinal cord injury. It is rare to have both hypotension and wheezing in such cases. In an anaphylactic reaction, an allergen, such as a food protein, medication, insect venom or latex, is introduced into the body. The mast cells of the immune system have a protein on their surface called IgE antibodies (Immunoglobulin E). The mast cells are filled with histamines [table: see text] and leukotrienes, which are chemical mediators. These are released when the allergen reacts with the IgE antibodies. When these mediators are released, they cause smooth-muscle constriction in the respiratory and gastrointestinal tracts, resulting in wheezing, stridor, nausea, vomiting and diarrhea. They also cause vascular dilation, leading to edema and urticaria. Most patients will present with either profound vascular effect (shock) or wheezing; this is a rather rare presentation of a patient having both. The medication best suited to counteract the effects of these medicators is epinephrine. Epinephrine is an alpha- and beta-agonist, acting to constrict the vasculature and dilate the smooth muscles in the bronchial tree. Antihistamines can alleviate symptoms of anaphylaxis, but should only be used in addition to epinephrine, not as a substitute. In life-threatening reactions, epinephrine must be given quickly and in a form that the body can distribute. Use of the subcutaneous route with a solution mixed at 1:1,000 dilution is appropriate in most patients, but if the patient is in profound shock and not perfusing the skin (pale, cold, clammy skin), then a more diluted concentration must be given i.v. at a slow rate (1 cc every minute of the 1:1,000 dilution) until the patient recovers. If i.v. access is delayed or not available, give the 1:1,000 dilution intramuscularly, in the tongue or down the endotracheal tube. Refer to your local protocols for dosage, but the usual dose of epinephrine is 0.3-0.5 mg, or 0.01 mg/kg in a child. There are more than 40 million people in the U.S. with allergic histories that place them at risk for developing anaphylaxis. Each year over 5,000 deaths are attributed to anaphylaxis. The risk of death from anaphylaxis increases with a more rapid onset of signs and symptoms. Up to 25% of patients will experience a biphasic reaction. This means there is a recurrence of symptoms several hours after the initial reaction, and it is prudent to observe patients for a period of time following their initial treatment.
这是一次非常成功的抢救。医护人员很容易就会忽略过敏反应的表现,从而错过使用肾上腺素治疗的时机。该患者处于过敏性休克状态。没有迹象表明存在创伤性损伤,再加上出汗、荨麻疹和心动过速的中心脉搏,这促使医生怀疑是过敏反应。过敏反应被归类为分布性休克。这种类型的休克是由严重的全身血管扩张引起的,心脏无法充分增加输出量以维持血压。分布性休克的其他原因包括败血症和脊髓损伤。在这种情况下,同时出现低血压和喘息的情况很少见。在过敏反应中,一种过敏原,如食物蛋白、药物、昆虫毒液或乳胶,被引入体内。免疫系统的肥大细胞表面有一种叫做IgE抗体(免疫球蛋白E)的蛋白质。肥大细胞充满了组胺[见表文]和白三烯,它们是化学介质。当过敏原与IgE抗体反应时,这些介质就会释放出来。当这些介质释放时,它们会导致呼吸道和胃肠道的平滑肌收缩,从而引起喘息、喘鸣、恶心、呕吐和腹泻。它们还会导致血管扩张,引发水肿和荨麻疹。大多数患者会表现出严重的血管效应(休克)或喘息;同时出现这两种症状的患者相当罕见。最适合对抗这些介质作用的药物是肾上腺素。肾上腺素是一种α和β受体激动剂,作用是收缩血管系统并扩张支气管树中的平滑肌。抗组胺药可以缓解过敏反应的症状,但只能在使用肾上腺素的基础上使用,而不能替代肾上腺素。在危及生命的反应中,必须迅速给予肾上腺素,且要采用身体能够吸收的剂型。大多数患者适合采用皮下注射1:1000稀释溶液的方式,但如果患者处于严重休克状态且皮肤灌注不良(皮肤苍白、冰冷、潮湿),则必须以较慢的速度静脉注射更稀释的浓度(1:1000稀释液每分钟1毫升),直到患者恢复。如果静脉通路延迟或无法建立,可以通过肌肉注射、舌部注射或经气管插管给予1:1000稀释液。请参考当地的用药方案确定剂量,但肾上腺素的常用剂量是0.3 - 0.5毫克,儿童为0.01毫克/千克。在美国,有超过4000万人有过敏史,有发生过敏反应的风险。每年有超过5000人死于过敏反应。过敏反应导致死亡的风险会随着症状和体征出现得更快而增加。高达25%的患者会出现双相反应。这意味着在初始反应数小时后症状会复发,因此在对患者进行初始治疗后,谨慎的做法是对其进行一段时间的观察。