ARDS - An Update - Part 1: Epidemiology, Pathophysiology and Diagnosis

被引:10
作者
Dembinski, Rolf [1 ,2 ,3 ]
Mielck, Frank [4 ,5 ,6 ,7 ]
机构
[1] Rhein Westfal TH Aachen, Anasthesiol Erwerb Zusatzqualifikat Intens Med &, Bereichsleitung Intens Stn Schwerverbrannte, Aachen, Germany
[2] Rhein Westfal TH Aachen, Aachen, Germany
[3] Klinikum Bremen Mitte, Klin Intens Med & Notfallmed, St Jurgen Str 1, D-28177 Bremen, Germany
[4] Univ Tubingen, Anasthesiol, Tubingen, Germany
[5] Univ Gottingen, Anasthesiol, Gottingen, Germany
[6] Univ Gottingen, Operat Intens Med, Zentrum Anasthesiol Rettungs & Intens Med, Gottingen, Germany
[7] Klinikum Bremen Mitte, Klin Intens & Notfallmed, Bremen, Germany
来源
ANASTHESIOLOGIE INTENSIVMEDIZIN NOTFALLMEDIZIN SCHMERZTHERAPIE | 2018年 / 53卷 / 02期
关键词
akute respiratorische Insuffizienz; Hypoxamie; Inflammation; Inzidenz; Letalitat; acute respiratory failure; hypoxemia; inflammation; incidence; mortality; RESPIRATORY-DISTRESS-SYNDROME; ACUTE LUNG INJURY; NEUTROPHIL ELASTASE; MORTALITY; BIOMARKERS; OUTCOMES; VENTILATION; DEFINITION; SURVIVAL; 50TH;
D O I
10.1055/s-0043-107166
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Zusammenfassung Das akute Lungenversagen (Acute respiratory Distress Syndrome, ARDS) ist inzwischen seit mehr als 50 Jahren als schwerwiegende Komplikation unterschiedlicher Grunderkrankungen gefurchtet [1]. Haufig leiden ARDS-Patienten langfristig unter schwerwiegenden Beeintrachtigungen - auch nach primar erfolgreicher Therapie. Der erste Teil dieses Updates gibt einen aktualisierten uberblick zu Definition, Epidemiologie und Pathophysiologie des ARDS. Abstract The Acute Respiratory Distress Syndrome (ARDS) is defined by hypoxemic respiratory failure caused by inflammatory response within the lung usually requiring invasive mechanical ventilation. Despite more than 50 years of research numerous issues regarding epidemiology, pathophysiology and diagnosis remain unclear until today: Due to rather unspecific clinical diagnostic criteria incidence of ARDS varies considerably in clinical trials with a range from 4 to 79 cases per 100000 persons per year. Consequently, mortality is also highly variable from about 40 to 60% in severe ARDS. Pathophysiology is mainly characterized by granulocyte infiltration of the lung thereby inducing interstitial and intra-alveolar lung edema with surfactant depletion and atelectasis formation. However, it is unknown whether pulmonary and extrapulmonary causes and risk factors for ARDS are accompanied by different pathophysiologic processes due to primary endothelial and epithelial injury. Thus, possible benefits of corresponding biomarker panels for the differentiation of endothelial and epithelial lung injury are also speculative until today. Therefore, ARDS diagnosis is still based on clinical findings and radiological imaging.
引用
收藏
页码:102 / 111
页数:10
相关论文
共 44 条
[1]   Clinical utility of the neutrophil elastase inhibitor sivelestat for the treatment of acute respiratory distress syndrome [J].
Aikawa, Naoki ;
Kawasaki, Yasushi .
THERAPEUTICS AND CLINICAL RISK MANAGEMENT, 2014, 10 :621-629
[2]  
Ashbaugh David G, 2005, Crit Care Resusc, V7, P60
[3]   Pulmonary ultrasound and pulse oximetry versus chest radiography and arterial blood gas analysis for the diagnosis of acute respiratory distress syndrome: a pilot study [J].
Bass, Cameron M. ;
Sajed, Dana R. ;
Adedipe, Adeyinka A. ;
West, T. Eoin .
CRITICAL CARE, 2015, 19
[4]   Epidemiology, Patterns of Care, and Mortality for Patients With Acute Respiratory Distress Syndrome in Intensive Care Units in 50 Countries [J].
Bellani, Giacomo ;
Laffey, John G. ;
Pham, Tai ;
Fan, Eddy ;
Brochard, Laurent ;
Esteban, Andres ;
Gattinoni, Luciano ;
van Haren, Frank ;
Larsson, Anders ;
McAuley, Daniel F. ;
Ranieri, Marco ;
Rubenfeld, Gordon ;
Thompson, B. Taylor ;
Wrigge, Hermann ;
Slutsky, Arthur S. ;
Pesenti, Antonio .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2016, 315 (08) :788-800
[5]   THE AMERICAN-EUROPEAN CONSENSUS CONFERENCE ON ARDS - DEFINITIONS, MECHANISMS, RELEVANT OUTCOMES, AND CLINICAL-TRIAL COORDINATION [J].
BERNARD, GR ;
ARTIGAS, A ;
BRIGHAM, KL ;
CARLET, J ;
FALKE, K ;
HUDSON, L ;
LAMY, M ;
LEGALL, JR ;
MORRIS, A ;
SPRAGG, R ;
COCHIN, B ;
LANKEN, PN ;
LEEPER, KV ;
MARINI, J ;
MURRAY, JF ;
OPPENHEIMER, L ;
PESENTI, A ;
REID, L ;
RINALDO, J ;
VILLAR, J ;
VANASBECK, BS ;
DHAINAUT, JF ;
MANCEBO, J ;
MATTHAY, M ;
MEYRICK, B ;
PAYEN, D ;
PERRET, C ;
FOWLER, AA ;
SCHALLER, MD ;
HUDSON, LD ;
HYERS, T ;
KNAUS, W ;
MATTHAY, R ;
PINSKY, M ;
BONE, RC ;
BOSKEN, C ;
JOHANSON, WG ;
LEWANDOWSKI, K ;
REPINE, J ;
RODRIGUEZROISIN, R ;
ROUSSOS, C ;
ANTONELLI, MA ;
BELOUCIF, S ;
BIHARI, D ;
BURCHARDI, H ;
LEMAIRE, F ;
MONTRAVERS, P ;
PETTY, TL ;
ROBOTHAM, J ;
ZAPOL, W .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 149 (03) :818-824
[6]   Incidence and mortality of acute lung injury and the acute respiratory distress syndrome in three Australian states [J].
Bersten, AD ;
Edibam, C ;
Hunt, T ;
Moran, J .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 165 (04) :443-448
[7]   A Pathophysiologic Approach to Biomarkers in Acute Respiratory Distress Syndrome [J].
Blondonnet, Raiko ;
Constantin, Jean-Michel ;
Sapin, Vincent ;
Jabaudon, Matthieu .
DISEASE MARKERS, 2016, 2016
[8]   Does my patient really have ARDS? [J].
Brochard, Laurent ;
Pham, Tai ;
Rubenfeld, Gordon .
INTENSIVE CARE MEDICINE, 2016, 42 (05) :656-658
[9]   Plasma receptor for advanced glycation end products and clinical outcomes in acute lung injury [J].
Calfee, C. S. ;
Ware, L. B. ;
Eisner, M. D. ;
Parsons, P. E. ;
Thompson, B. T. ;
Wickersham, N. ;
Matthay, M. A. .
THORAX, 2008, 63 (12) :1083-1089
[10]  
Castillo R L, 2015, Open Respir Med J, V9, P83, DOI 10.2174/1874306401509010083