疟疾的肺部表现:识别和管理。

Walter R J Taylor, Viviam Cañon, Nicholas J White
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引用次数: 48

摘要

早在200多年前,人们就认识到疟疾对肺部的影响,但我们对其发病机制和管理的了解有限。肺水肿是肺部受累最严重的形式。肺泡毛细血管通透性增加导致血管内液体流失到肺部是主要的病理生理机制。这将疟疾定义为急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)的另一个原因。肺水肿最常被描述为恶性疟原虫感染的无免疫力个体的严重全身性疾病的一部分或急性疟疾的主要特征。间日疟和卵形疟也很少引起肺水肿。临床上,患者通常表现为急性呼吸困难,可在发病时迅速发展为呼吸衰竭,有趣的是,在治疗后,当临床改善和寄生虫血症下降时。孕妇特别容易发生肺水肿。疟疾引起的ALI/ARDS的最佳管理包括早期识别和诊断。从疟疾流行国家返回的旅行者或患有急性发热性疾病的访客必须始终怀疑患有疟疾。玻片镜检和/或使用快速抗原检测是标准的诊断工具。疟疾必须用有效的药物治疗,但目前的选择很少:例如,注射青蒿素、静脉注射奎宁或奎尼丁(仅在美国)。最近在成人中进行的一项试验表明,与静脉注射奎宁治疗的成人相比,静脉注射青蒿琥酯可使严重疟疾死亡率降低三分之一。呼吸损害应根据其优点进行管理,可能需要机械通气。患者应在重症监护病房接受治疗,并应特别注意积极治疗其他严重疟疾并发症,特别是昏迷和急性肾衰竭。ALI/ARDS也可能与偶然的细菌性败血症有关,但可能在临床上不明显。临床医生应采用较低的阈值,在采取相关的微生物标本后,对此类患者开始使用广谱抗菌药物。尽管有最佳的管理,严重疟疾合并急性呼吸窘迫综合征的预后很差。小儿疟疾中的ALI/ARDS似乎很少见。然而,伴有严重代谢性酸中毒或急性肺水肿的恶性疟疾可能表现为肺炎的临床表现,即呼吸急促、肋间退缩、喘息或吸气性心悸。这导致诊断混乱和治疗不理想。虽然疟疾流行国家日益认识到这一点,但温带地区的临床医生应该意识到,疟疾可能是到访或返回儿童“肺炎”的一个可能原因。
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Pulmonary manifestations of malaria : recognition and management.

Lung involvement in malaria has been recognized for more than 200 hundred years, yet our knowledge of its pathogenesis and management is limited. Pulmonary edema is the most severe form of lung involvement. Increased alveolar capillary permeability leading to intravascular fluid loss into the lungs is the main pathophysiologic mechanism. This defines malaria as another cause of acute lung injury (ALI) and acute respiratory distress syndrome (ARDS).Pulmonary edema has been described most often in non-immune individuals with Plasmodium falciparum infections as part of a severe systemic illness or as the main feature of acute malaria. P.vivax and P.ovale have also rarely caused pulmonary edema.Clinically, patients usually present with acute breathlessness that can rapidly progress to respiratory failure either at disease presentation or, interestingly, after treatment when clinical improvement is taking place and the parasitemia is falling. Pregnant women are particularly prone to developing pulmonary edema. Optimal management of malaria-induced ALI/ARDS includes early recognition and diagnosis. Malaria must always be suspected in a returning traveler or a visitor from a malaria-endemic country with an acute febrile illness. Slide microscopy and/or the use of rapid antigen tests are standard diagnostic tools. Malaria must be treated with effective drugs, but current choices are few: e.g. parenteral artemisinins, intravenous quinine or quinidine (in the US only). A recent trial in adults has shown that intravenous artesunate reduces severe malaria mortality by a third compared with adults treated with intravenous quinine. Respiratory compromise should be managed on its merits and may require mechanical ventilation.Patients should be managed in an intensive care unit and particular attention should be paid to the energetic management of other severe malaria complications, notably coma and acute renal failure. ALI/ARDS may also be related to a coincidental bacterial sepsis that may not be clinically obvious. Clinicians should employ a low threshold for starting broad spectrum antibacterials in such patients, after taking pertinent microbiologic specimens. Despite optimal management, the prognosis of severe malaria with ARDS is poor.ALI/ARDS in pediatric malaria appears to be rare. However, falciparum malaria with severe metabolic acidosis or acute pulmonary edema may present with a clinical picture of pneumonia, i.e. with tachypnea, intercostal recession, wheeze or inspiratory crepitations. This results in diagnostic confusion and suboptimal treatment. Whilst this is increasingly being recognized in malaria-endemic countries, clinicians in temperate zones should be aware that malaria may be a possible cause of 'pneumonia' in a visiting or returning child.

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