|Year : 2018 | Volume
| Issue : 10 | Page : 1220-1224
Acute Respiratory Distress Syndrome: Challenge for Diagnosis and Therapy
Chun Pan, Ling Liu, Jian-Feng Xie, Hai-Bo Qiu
Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, Jiangsu 210009, China
|Date of Submission||31-Jan-2018|
|Date of Web Publication||30-Apr-2018|
Dr. Hai-Bo Qiu
Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, Jiangsu 210009
Source of Support: None, Conflict of Interest: None
Objective: Acute respiratory distress syndrome (ARDS) is a devastating clinical syndrome whose diagnosis and therapy are still in question. The aim of this review was to discuss the current challenge for the diagnosis and treatment of ARDS.
Data Sources: Data sources were the published articles in English through December 2017 in PubMed using the following key words: “acute respiratory distress syndrome,” “definition”, “diagnosis,” “therapy,” “lung protective strategy,” “right ventricular dysfunction,” and “molecular mechanism.”
Study Selection: The selection of studies focused on both preclinical studies and clinical studies of therapy of ARDS.
Results: The incidence of ARDS is still high, and ARDS causes high intensive care units admissions and high mortality. The Berlin Definition proposed in 2012 is still controversial owing to lack of sensitivity and specificity. ARDS is still under recognition and it is associated with high mortality. Lung protective strategies with low tidal volume (VT) and lung recruitment should consider the physiology of ARDS because ARDS presents lung inhomogeneity; the same low VT might increase local stress and strain in some patients with low compliance, and lung recruitment could injure lungs in ARDS patients with low recruitability and hemodynamic instability. Acute cor pulmonale is common in severe ARDS. ARDS itself and some treatments could worsen acute cor pulmonale. Molecular understanding of the pathogenic contributors to ARDS has improved, but the molecular-associated treatments are still under development.
Conclusions: ARDS is a devastating clinical syndrome whose incidence and mortality has remained high over the past 50 years. Its definition and treatments are still confronted with challenges, and early recognition and intervention are crucial for improving the outcomes of ARDS. More clinical studies are needed to improve early diagnosis and appropriate therapy.
Keywords: Acute Respiratory Distress Syndrome; Diagnosis; Mechanical Ventilation; Therapy
|How to cite this article:|
Pan C, Liu L, Xie JF, Qiu HB. Acute Respiratory Distress Syndrome: Challenge for Diagnosis and Therapy. Chin Med J 2018;131:1220-4
|How to cite this URL:|
Pan C, Liu L, Xie JF, Qiu HB. Acute Respiratory Distress Syndrome: Challenge for Diagnosis and Therapy. Chin Med J [serial online] 2018 [cited 2018 Jul 18];131:1220-4. Available from: http://www.cmj.org/text.asp?2018/131/10/1220/228765
| Introduction|| |
Acute respiratory distress syndrome (ARDS) is a devastating clinical syndrome caused by various conditions such as infection and trauma. During the last five decades, a better understanding of the epidemiology, pathophysiology, and pathogenesis of ARDS has led to new treatment strategies that improved survival rates significantly in patients with ARDS. However, the mortality of severe ARDS is still over 40.0%. Early recognition of ARDS and optimized management are crucial for outcome improvement.
| Huge Burden of Acute Respiratory Distress Syndrome|| |
ARDS is a common disease with a high variation of incidence worldwide. Epidemiological studies of ARDS have revealed an incidence of 10.1 per 100,000 person-years in South America, 17.9/100,000 person-years in Europe, 34/100,000 person-years in Australia, and 78.9/100,000 person-years in the USA.,,,
In intensive care units (ICUs), the incidence of ARDS is 7.1–12.5% in European countries. A global study conducted over fifty countries showed that 10.4% (95% confidence interval [CI], 10.0–10.7%) ICU patients developed ARDS. Similarly, variation was found in this study with an incidence of 0.48, 0.46, 0.31, 0.27, 0.32, and 0.57 cases per ICU bed over 4 weeks in Europe, North America, South America, Asia, Africa, and Oceania, respectively. Compared to non-ARDS patients, the mortality of ARDS patients is significantly higher (29.0% vs. 12.0%). More importantly, mortality increases to over 40.0% when patients progress to severe ARDS. Therefore, it is urgent for clinicians to achieve early recognition and diagnosis.
| The Berlin Definition of Acute Respiratory Distress Syndrome Is Commonly Used But Not Perfect|| |
It has been 50 years since Ashbaugh et al. first termed “ARDS” as a syndrome characterized by “acute onset of tachypnea, hypoxemia, and loss of compliance after a variety of stimuli” in 1967. Since then, it has been a long path to define ARDS. There is much controversy in the definition of ARDS from the “Murray Lung Injury Score” to “the American-European Consensus Conference (AECC) definition” to “the Berlin definition.”
Compared with the AECC definition, the Berlin definition specifies the following: acute onset within 1 week; the source of lung edema, considering the coexistence of cardiogenic pulmonary edema and original disease factors; characteristics of the bilateral lung infiltrates on the chest X-ray or CT scan; hypoxemia evaluated with a positive end-expiratory pressure (PEEP) level ≥5 cmH2O (1 cmH2O = 0.098 kPa); and lung injury divided into three grades of severity according to the partial pressure of oxygen in arterial blood/fraction of inspired oxygen (PaO2/FiO2) ratio. The predictive validity for mortality was significantly improved by the Berlin definition of ARDS.
However, the definition is still controversial. First, the current clinical tools cannot identify the pathological change of ARDS; second, the lack of a specific biomarker might influence diagnostic specificity; and third, the stratification of ARDS patients as proposed by the Berlin criteria is less useful for assessing the severity of lung injury and depends on the patient's therapeutic response. More than 60.0% of patients with severe ARDS according to the Berlin criteria were reclassified as moderate, mild, or non-ARDS after 24 h of usual care, and hospital mortality changed significantly. Finally, although the Berlin definition has higher predictive validity for mortality than the AECC definition, the specificity of the Berlin definition for ARDS was relatively poor when using diffuse alveolar damage as the reference standard, and the predictive validity of the Lung Injury Score for mortality was similar to the Berlin definition stages of severity with an area under the curve of 0.58 compared to 0.60.,
| Acute Respiratory Distress Syndrome Is Still under Recognition|| |
ARDS could worsen patients' prognosis, and the mortality between ARDS and non-ARDS is significantly different. In the Large Observational Study to Understand the Global Impact of Severe Acute Respiratory Failure (Lung SAFE) study, 60.2% of all patients with ARDS were clinician recognized, and the clinician's diagnosis of ARDS ranged from 51.3% (95% CI, 47.5–55.0%) for mild ARDS to 78.5% (95% CI, 74.8–81.8%) for severe ARDS.
Several factors influence the early diagnosis of ARDS. Higher nurse-to-patient ratios, higher physician-to-patient ratios, younger patient age, lower PaO2/FiO2 ratio, and the presence of pneumonia or pancreatitis were factors independently associated with higher probability of clinician recognition.
There are still some factors associated with a lower probability of early recognition of ARDS. Absence of a risk factor and presence of concomitant cardiac failure were associated with reduced likelihood of clinician recognition of ARDS.,
| Tidal Volume Should Be Individualized|| |
Although low tidal volume (VT) has been proved to decrease ARDS mortality, 6 ml/kg predicted body weight (PBW) VT is not suitable for all ARDS patients. Terragni et al. found that VT of 6 ml/kg PBW and plateau pressure of 30 cmH2O might not be sufficient to protect two-third of ARDS patients from dynamic hyperinflation. In fact, nonphysiological lung strain and stress could induce ventilator-induced lung injury (VILI), either globally or locally. It has been found that dynamic strain is still higher in many ARDS patients ventilated with even 6 ml/kg PBW. To minimize VILI, it is more reasonable to normalize VT to individual lung size. A former study showed that pulmonary compliance is associated with end-expiratory lung volume (EELV)., To address this issue, airway driving pressure (quotient of VT/Crs) is proposed to substitute for lung dynamic strain. Amato et al. used multilevel mediation analysis to analyze individual data from 3562 patients with ARDS enrolled in nine randomized trials; they showed that decreases in driving pressure due to changes in ventilator settings were strongly associated with increased survival. Further study is needed to demonstrate whether driving pressure could be a goal of the individualized setting of VT in itself.
Airway driving pressure could be used as a safety limit during VT titration at the bedside. It has been demonstrated that driving pressure during mechanical ventilation is directly related to stress forces in the lung. Optimal cutoff values for airway driving pressure of 15.0 cmH2O and 16.6 cmH2O were considered as stress equal to or greater than 24 cmH2O and 26 cmH2O, respectively. In the clinical scenario, airway driving pressure is affected by chest wall compliance and spontaneous breathing. Inhibition of spontaneous breathing might be necessary during the measurement of airway driving pressure. However, routine measurement of transpulmonary driving pressure is not suggested since linear regression between transpulmonary and airway driving pressure has been found in 150 ARDS patients.
In severe ARDS patients, a lower VT strategy for lung protection might be followed by refractory hypoxemia or hypercapnia. In this scenario, extracorporeal membrane oxygenation (ECMO) or extracorporeal CO2 elimination should be used as the first-line rescue treatment to improve oxygenation or CO2 elimination. Positive results of the CESAR trial have led to an exponential use of these technologies in the recent years. The initial time of ECMO in patients with ARDS remains controversial, but the early use of ECMO could protect lungs from VILI. Indeed, ECMO is one of the most effective methods for lung protection, allowing very low VT leading to “lung rest.”
| Pathophysiological Characteristics Guiding Lung Recruitment and Positive End-Expiratory Pressure Titration|| |
Lung recruitment maneuvers (RMs) will be beneficial when properly applied to appropriately selected patients with high lung recruitability. A meta-analysis of six clinical trials has suggested RMs with higher PEEP-reduced mortality in patients with moderate and severe ARDS, but this finding has not been confirmed in randomized clinical trials.,, Recently, a large randomized clinical trial compared patients treated with the RMs and titrated PEEP (n = 501) with those managed with conventional PEEP (n = 509) in moderate-to-severe ARDS (PaO2/FiO2 200). The result showed that a strategy with lung recruitment and titrated PEEP compared with the control group increased 28-day all-cause mortality, and RMs were associated with pulmonary complication in patients with moderate-to-severe ARDS. There are several reasons for the surprising results. First, RMs are suitable for high recruitability patients, but this study recruited more pneumonia patients, which had been demonstrated to have low lung recruitability; second, the pressure in the RM group is higher than that in former studies, which could increase the incidence of pneumothorax and barotrauma, complications of which are disastrous for severe ARDS; third, there are more septic shock patients in this study, and RMs could lead to hemodynamic variation, which might be the reason why the mortality is high in the RM group; fourth, the relatively high recruitment pressure will deteriorate hemodynamic stability and lead to more fluid administration; and fifth, RMs might be more beneficial in the early phase of ARDS, but the RMs were used for 7 days in this study. RMs remind clinician, not only severity of ARDS, but lung recruitability, phase of ARDS, recruitment pressure limitation, and hemodynamic stability should also be considered.
Prone position ventilation is another method of lung recruitment, especially for ARDS patients with low lung recruitability. Due to its beneficial effects in improving ventilation-perfusion matching, increasing EELV, and decreasing VILI by a more uniform distribution of VT through lung recruitment and alterations in chest wall mechanics, prone position ventilation should be considered in the early phase of ARDS in patients with PaO2/FiO2<150 mmHg (1 mmHg = 0.133 kPa). According to the study of Guérin et al. in patients with severe ARDS, early application of prolonged prone-positioning sessions for at least 16 h significantly decreased 28-day and 90-day mortality. With respect to the duration of the prone position, it has been strongly recommended that adult patients with severe ARDS receive prone positioning for more than 12 h/day.
Although the optimal approach to PEEP titration has not yet been established, oxygenation-based PEEP titration is the most commonly used method related to lung recruitability. The ARDSNet FiO2-PEEP table is one of the simple oxygenation-based methods for initial PEEP setting. Furthermore, the oxygenation response should be considered during PEEP titration. Goligher et al. found that patients with a positive oxygenation response (>25 mmHg increase in PaO2/FiO2) of higher PEEP had lower mortality than those without a positive oxygenation response (crude mortality rate: 31.0% vs. 54.0%, adjusted odds ratio [OR]: 0.36, 95% CI: 0.23–0.58). These results indicated that higher PEEP will benefit patients with a positive oxygenation response of PEEP. Since lung recruitability is associated with the severity of ARDS, setting PEEP according to ARDS severity might be a simple but physiologically sound method. Gattinoni et al. suggested that PEEP ranges of 5–10, 10–15, and >15 cmH2O should be used in mild, moderate, and severe ARDS, respectively. Individualized PEEP titrated by EIT, compliance, and transpulmonary pressure are helpful in selected ARDS patients.
| Acute Cor Pulmonale Should Not Be Ignored|| |
Acute cor pulmonale (ACP) is common in severe ARDS patients and is always ignored. The prevalence rate of echocardiographically evident ACP in ARDS ranges from 22.0% to 50.0%. Treatment of ACP in ARDS includes optimization of right ventricle preload and afterload; increased right ventricle contractility, pulmonary vasodilators, and lung protective ventilation are the important methods for reducing right ventricle afterload. For severe ACP, RMs, prone ventilation, and extracorporeal life support can reverse the physiological causes of ACP and facilitate “RV-protective” ventilation; however, ARDS mortality has not been verified in clinical studies.
| Understanding of Molecular Mechanism for Acute Respiratory Distress Syndrome|| |
Novel analytical techniques have been conducted for some of these accepted markers to refine ARDS endotypes or to serve as enrichment markers in future trials. Genome-wide association studies, next-generation sequencing, gene expression profiling, proteomics and metabolomics, and microbiome analysis have been used to select genetic variation and changes of expression of proteins and metabolites. Improved molecular understanding of the pathogenic contributors to ARDS could lead to individualized therapy for the inhomogeneous syndrome and could improve outcomes in the future.
ARDS has been a devastating clinical syndrome during the past 50 years, and its incidence and mortality remain high. The definition and treatment of ARDS are still confronted with challenges, and early recognition and intervention is crucial for improving the outcomes of ARDS. Precise lung protective strategy and early use of ECMO could improve the mortality rate of severe ARDS. More clinical studies are needed to improve early diagnosis and appropriate therapy.
Financial support and sponsorship
This work was supported by grants from the National Natural Science Foundation of China (No. 81372093, No. 81670074, No. 81571847, and No. 81300043), Jiangsu Provincial Medical Youth Talent (No. QNRC2016807), and Jiangsu Medical Key Disciplines Project (No. ZDXKA2016025).
Conflicts of interest
There are no conflicts of interest.
| References|| |
Laffey JG, Bellani G, Pham T, Fan E, Madotto F, Bajwa EK, et al
. Potentially modifiable factors contributing to outcome from acute respiratory distress syndrome: The LUNG SAFE study. Intensive Care Med 2016;42:1865-76. doi: 10.1007/s00134-016-4571-5.
Bellani G, Laffey JG, Pham T, Fan E, Brochard L, Esteban A, et al
. Epidemiology, patterns of care, and mortality for patients with acute respiratory distress syndrome in Intensive Care Units in 50 countries. JAMA 2016;315:788-800. doi: 10.1001/jama.2016.0291.
Caser EB, Zandonade E, Pereira E, Gama AM, Barbas CS. Impact of distinct definitions of acute lung injury on its incidence and outcomes in Brazilian ICUs: Prospective evaluation of 7,133 patients. Crit Care Med 2014;42:574-82. doi: 10.1097/01.ccm.0000435676.68435.56.
Hughes M, Grant IS, MacKirdy FN. Incidence and mortality after acute respiratory failure and acute respiratory distress syndrome in Sweden, Denmark, and Iceland. Am J Respir Crit Care Med 2000;162:332-3. doi: 10.1164/ajrccm.162.1.16213b.
Bersten AD, Edibam C, Hunt T, Moran J; Australian and New Zealand Intensive Care Society Clinical Trials Group. Incidence and mortality of acute lung injury and the acute respiratory distress syndrome in three Australian states. Am J Respir Crit Care Med 2002;165:443-8.doi: 10.1164/ajrccm.165.4.2101124.
Rubenfeld GD, Caldwell E, Peabody E, Weaver J, Martin DP, Neff M, et al
. Incidence and outcomes of acute lung injury. N
Engl J Med 2005;353:1685-93. doi: 10.1056/NEJMoa050333.
Ashbaugh DG, Bigelow DB, Petty TL, Levine BE. Acute respiratory distress in adults. Lancet 1967;2:319-23. doi: 10.1016/S0140-6736(67)90168-7.
Ferguson ND, Fan E, Camporota L, Antonelli M, Anzueto A, Beale R, et al
. The Berlin definition of ARDS: An expanded rationale, justification, and supplementary material. Intensive Care Med 2012;38:1573-82. doi: 10.1007/s00134-012-2682-1.
Villar J, Pérez-Méndez L, Kacmarek RM. The Berlin definition met our needs: No. Intensive Care Med 2016;42:648-50. doi: 10.1007/s00134-016-4242-6.
Villar J, Blanco J, del Campo R, Andaluz-Ojeda D, Díaz-Domínguez FJ, Muriel A, et al
. Assessment of PaO2
for stratification of patients with moderate and severe acute respiratory distress syndrome. BMJ Open 2015;5:e006812. doi: 10.1136/bmjopen-2014-006812.
Kangelaris KN, Calfee CS, May AK, Zhuo H, Matthay MA, Ware LB, et al
. Is there still a role for the lung injury score in the era of the Berlin definition ARDS? Ann Intensive Care 2014;4:4. doi: 10.1186/2110-5820-4-4.
Thompson BT, Matthay MA. The Berlin definition of ARDS versus pathological evidence of diffuse alveolar damage. Am J Respir Crit Care Med 2013;187:675-7. doi: 10.1164/rccm.201302-0385ED.
Summers C, Singh NR, Worpole L, Simmonds R, Babar J, Condliffe AM, et al
. Incidence and recognition of acute respiratory distress syndrome in a UK Intensive Care Unit. Thorax 2016;71:1050-1. doi: 10.1136/thoraxjnl-2016-208402.
Bellani G, Laffey JG, Pham T, Fan E; LUNG SAFE Investigators and the ESICM Trials Group. The LUNG SAFE study: A presentation of the prevalence of ARDS according to the Berlin definition! Crit Care 2016;20:268. doi: 10.1186/s13054-016-1443-x.
Weiss CH, Baker DW, Tulas K, Weiner S, Bechel M, Rademaker A, et al
. Acritical care clinician survey comparing attitudes and perceived barriers to low tidal volume ventilation with actual practice. Ann Am Thorac Soc 2017;14:1682-9. doi: 10.1513/AnnalsATS.201612-973OC.
Terragni PP, Rosboch G, Tealdi A, Corno E, Menaldo E, Davini O, et al
. Tidal hyperinflation during low tidal volume ventilation in acute respiratory distress syndrome. Am J Respir Crit Care Med 2007;175:160-6. doi: 10.1164/rccm.200607-915OC.
Chiumello D, Carlesso E, Cadringher P, Caironi P, Valenza F, Polli F, et al
. Lung stress and strain during mechanical ventilation for acute respiratory distress syndrome. Am J Respir Crit Care Med 2008;178:346-55. doi: 10.1164/rccm.200710-1589OC.
Xie J, Jin F, Pan C, Liu S, Liu L, Xu J, et al
. The effects of low tidal ventilation on lung strain correlate with respiratory system compliance. Crit Care 2017;21:23. doi: 10.1186/s13054-017-1600-x.
Casserly B, McCool FD, Saunders J, Selvakumar N, Levy MM. End-expiratory volume and oxygenation: Targeting PEEP in ARDS patients. Lung 2016;194:35-41. doi: 10.1007/s00408-015-9823-6.
Protti A, Andreis DT, Monti M, Santini A, Sparacino CC, Langer T, et al
. Lung stress and strain during mechanical ventilation: Any difference between statics and dynamics? Crit Care Med 2013;41:1046-55. doi: 10.1097/CCM.0b013e31827417a6.
Amato MB, Meade MO, Slutsky AS, Brochard L, Costa EL, Schoenfeld DA, et al
. Driving pressure and survival in the acute respiratory distress syndrome. N
Engl J Med 2015;372:747-55. doi: 10.1056/NEJMsa1410639.
Chiumello D, Carlesso E, Brioni M, Cressoni M. Airway driving pressure and lung stress in ARDS patients. Crit Care 2016;20:276. doi: 10.1186/s13054-016-1446-7.
Peek GJ, Mugford M, Tiruvoipati R, Wilson A, Allen E, Thalanany MM, et al
. Efficacy and economic assessment of conventional ventilatory support versus extracorporeal membrane oxygenation for severe adult respiratory failure (CESAR): A multicentre randomised controlled trial. Lancet 2009;374:1351-63. doi: 10.1016/S0140-6736(09)61069-2.
Pham T, Combes A, Rozé H, Chevret S, Mercat A, Roch A, et al
. Extracorporeal membrane oxygenation for pandemic influenza A (H1N1)-induced acute respiratory distress syndrome: A cohort study and propensity-matched analysis. Am J Respir Crit Care Med 2013;187:276-85. doi: 10.1164/rccm.201205-0815OC.
Brower RG, Lanken PN, MacIntyre N, Matthay MA, Morris A, Ancukiewicz M, et al
. Higher versus lower positive end-expiratory pressures in patients with the acute respiratory distress syndrome. N
Engl J Med 2004;351:327-36. doi: 10.1056/NEJMoa032193.
Meade MO, Cook DJ, Guyatt GH, Slutsky AS, Arabi YM, Cooper DJ, et al
. Ventilation strategy using low tidal volumes, recruitment maneuvers, and high positive end-expiratory pressure for acute lung injury and acute respiratory distress syndrome: A randomized controlled trial. JAMA 2008;299:637-45. doi: 10.1001/jama.299.6.637.
Mercat A, Richard JC, Vielle B, Jaber S, Osman D, Diehl JL, et al
. Positive end-expiratory pressure setting in adults with acute lung injury and acute respiratory distress syndrome: A randomized controlled trial. JAMA 2008;299:646-55. doi: 10.1001/jama.299.6.646.
Writing Group for the Alveolar Recruitment for Acute Respiratory Distress Syndrome Trial (ART) Investigators, Cavalcanti AB, Suzumura ÉA, Laranjeira LN, Paisani DM, Damiani LP, et al
. Effect of lung recruitment and titrated positive end-expiratory pressure (PEEP) vs. low PEEP on mortality in patients with acute respiratory distress syndrome: A Randomized Clinical Trial. JAMA 2017;318:1335-45. doi: 10.1001/jama.2017.14171.
Sahetya SK, Brower RG. Lung recruitment and titrated PEEP in moderate to severe ARDS: Is the door closing on the open lung? JAMA 2017;318:1327-9. doi: 10.1001/jama.2017.13695.
Guérin C, Reignier J, Richard JC, Beuret P, Gacouin A, Boulain T, et al
. Prone positioning in severe acute respiratory distress syndrome. N
Engl J Med 2013;368:2159-68. doi: 10.1056/NEJMoa1214103.
Fan E, Del Sorbo L, Goligher EC, Hodgson CL, Munshi L, Walkey AJ, et al
. An Official American Thoracic Society/European Society of Intensive Care Medicine/Society of Critical Care Medicine Clinical Practice Guideline: Mechanical ventilation in adult patients with acute respiratory distress syndrome. Am J Respir Crit Care Med 2017;195:1253-63. doi: 10.1164/rccm.201703-0548ST.
Goligher EC, Kavanagh BP, Rubenfeld GD, Adhikari NK, Pinto R, Fan E, et al
. Oxygenation response to positive end-expiratory pressure predicts mortality in acute respiratory distress syndrome. A secondary analysis of the LOVS and ExPress trials. Am J Respir Crit Care Med 2014;190:70-6. doi: 10.1164/rccm.201404-0688OC.
Gattinoni L, Carlesso E, Brazzi L, Cressoni M, Rosseau S, Kluge S,et al
. Friday night ventilation: A safety starting tool kit for mechanically ventilated patients. Minerva Anestesiol 2014;80:1046-57.
Mekontso Dessap A, Boissier F, Charron C, Bégot E, Repessé X, Legras A, et al
. Acute cor pulmonale during protective ventilation for acute respiratory distress syndrome: Prevalence, predictors, and clinical impact. Intensive Care Med 2016;42:862-70. doi: 10.1007/s00134-015-4141-2.
Repessé X, Charron C, Vieillard-Baron A. Acute cor pulmonale in ARDS: Rationale for protecting the right ventricle. Chest 2015;147:259-65. doi: 10.1378/chest.14-0877.