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Management of acute respiratory failure in interstitial lung diseases: overview and clinical insights
BMC Pulmonary Medicine volume 18, Article number: 70 (2018)
Interstitial lung diseases (ILDs) are a heterogeneous group of diseases characterized by widespread fibrotic and inflammatory abnormalities of the lung. Respiratory failure is a common complication in advanced stages or following acute worsening of the underlying disease. Aim of this review is to evaluate the current evidence in determining the best management of acute respiratory failure (ARF) in ILDs.
A literature search was performed in the Medline/PubMed and EMBASE databases to identify studies that investigated the management of ARF in ILDs (the last search was conducted on November 2017).
In managing ARF, it is important to establish an adequate diagnostic and therapeutic management depending on whether the patient has an underlying known chronic ILD or ARF is presenting in an unknown or de novo ILD. In the first case both primary causes, such as acute exacerbations of the disease, and secondary causes, including concomitant pulmonary infections, fluid overload and pulmonary embolism need to be investigated. In the second case, a diagnostic work-up that includes investigations in regards to ILD etiology, such as autoimmune screening and bronchoalveolar lavage, should be performed, and possible concomitant causes of ARF have to be ruled out.
Oxygen supplementation and ventilatory support need to be titrated according to the severity of ARF and patients’ therapeutic options. High-Flow Nasal oxygen might potentially be an alternative to conventional oxygen therapy in patients requiring both high flows and high oxygen concentrations to correct hypoxemia and control dyspnea, however the evidence is still scarce. Neither Non-Invasive Ventilation (NIV) nor Invasive Mechanical Ventilation (IMV) seem to change the poor outcomes associated to advanced stages of ILDs. However, in selected patients, such as those with less severe ARF, a NIV trial might help in the early recognition of NIV-responder patients, who may present a better short-term prognosis. More invasive techniques, including IMV and Extracorporeal Membrane Oxygenation, should be limited to patients listed for lung transplant or with reversible causes of ARF.
Despite the overall poor prognosis of ARF in ILDs, a personalized approach may positively influence patients’ management, possibly leading to improved outcomes. However, further studies are warranted.
Interstitial lung diseases (ILDs) are a heterogeneous group of diseases that includes more than 200 entities characterized by widespread fibrotic and/or inflammatory abnormalities of the lung parenchyma, Fig. 1 [1, 2]. Respiratory failure is a common complication in advanced stages or following acute worsening of ILDs and can be classified on the basis of different parameters, including time of onset (acute or chronic), severity (mild to severe), and causes (reversible or irreversible).
Aim of this review is to evaluate the current evidence in determining the best management of acute respiratory failure (ARF) in ILDs.
A search of relevant medical literature in the English language was conducted in Medline/PubMed and EMBASE databases including observational and interventional studies from 1990 through November 2017. Keywords used to perform the research are reported in Table 1. Studies targeting children and editorials, narrative, and conference abstracts have been excluded. For the purpose of this review, any kind of ILD was included in the search.
Results and discussion
Epidemiology and risk factors
In recent times, ILDs definitions and classifications have been extensively revised , therefore it is difficult to provide precise epidemiological data for each class of ILD. In the present review we will mostly address idiopathic pulmonary fibrosis (IPF), which is the most widely studied ILD.
From a study conducted in New Mexico, USA, it was estimated that the prevalence of ILDs was approximately 81 / 100,000 in men and 64 / 100,000 in females . The same study showed a higher incidence in males (31.5 per 100,000 / year) than females (26.1 per 100,000 / year) . Both prevalence and incidence vary greatly depending on the specific type of ILD considered. In particular, although classified as rare diseases, the two most frequently diagnosed ILDs are IPF and sarcoidosis.
IPF has a prevalence of 0.5–27 / 100,000 and an incidence of 0.22–8.8 / 100,000 inhabitants worldwide . When focusing on European data, the prevalence of IPF is 1.25–23.4 / 100,000, and the annual incidence 0.22–7.4 / 100,000 . The incidence of acute exacerbation (AE) of IPF ranges between 0 and 21% according to different cohorts [6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26], and predominantly occurs in advanced stages of the disease [13, 27,28,29]. This highly variable incidence is probably due to differences in study design (prospective vs retrospective), definition of AE and statistical methodology . Recognized risk factors for AE of IPF (AE-IPF) are lower forced vital capacity and diffusion capacity of carbon monoxide as well as reduced walked distance at 6-min walking test [13, 24, 27, 30,31,32], worsening respiratory gas exchange , higher dyspnea scores , greater disease extent on high-resolution computed tomography (HRCT) as well as presence and extent of honeycombing and traction bronchiectasis , presence of gastroesophageal reflux disease [34, 35], exposure to air pollution , presence of pulmonary hypertension , specific genetic variants , drug toxicity, bronchoalveolar lavage , surgical lung biopsy [39, 40], and surgery, radiotherapy or chemotherapy for concomitant lung cancer [28, 41,42,43]. Other non-validated risk factors are elevated baseline serum Krebs von der Lungen-6 (KL-6) [44, 45], increased body mass index , younger age , and concomitant coronary artery disease , whereas data on smoke exposure and emphysema as risk factors are discordant .
Outcome of different interstitial lung diseases
IPF is the ILD with the worst prognosis, having a median survival of 2 to 3 years from the time of diagnosis . In 2003 in the USA, the mortality rate related to IPF was 61.2 deaths per 1,000,000 in men and 54.5 deaths per 1,000,000 in women . AE-IPF is the most common cause of mortality in IPF cohorts [48, 49], accounting for over half of all hospitalizations  and up to 40% of all deaths . Prognosis of AE-IPF is extremely poor with a in-hospital mortality rate around 50% in less severe patients and higher than 90% in those requiring Intensive Care Unit (ICU) admission [12, 13, 50,51,52,53,54,55].
Connective tissue disease related ILD (CTD-ILD) has a better prognosis compared to IPF, as emerged from a UK study by Navaratnam et al. , with a median survival of 6.5 vs 3.1 years in patients with IPF. Among ILDs, sarcoidosis is the one with the best prognosis; Thomeer et al. compared the mortality of different forms of ILDs in a tertiary care hospital setting: the 5-year survival of patients with sarcoidosis was 91.6% compared to 69.7% for CTD-ILD and 35% for IPF .
Despite the high mortality associated to ARF in all ILDs, IPF showed higher one-year mortality after hospitalization for acute respiratory worsening compared to patients with other fibrotic ILDs, (87% vs 71%, respectively) . Median survival after an AE-IPF ranges between 22 days and 4.2 months [13, 24].
Underlying pathophysiology of acute respiratory failure in interstitial lung diseases
ARF may occur as an acute/subacute presentation of ILD or may complicate the clinical course of a previously diagnosed ILD or unknown ILD as the result of the rapid decline of respiratory function caused by an accelerated worsening of the underlying interstitial process, the so-called AE, or because of superimposed complications, such as pulmonary thromboembolism, heart failure and infection .
AE-ILD might be the consequence of an intrinsic acceleration of the fibroproliferative process or a response to occult or known external events (e.g. infection, micro-aspiration or mechanical stretch such as lung biopsies) .
The histopathological hallmark of AE-ILDs, particularly AE-IPF, is diffuse alveolar damage (DAD), superimposed on the histological pattern of the underlying ILD [11, 59,60,61]. DAD presents histologically with two subsequent phases, an acute/exudative phase followed by an organizing/prolipherative phase, that sometimes evolves in a final fibrotic stage.
The acute exudative phase is characterized by relatively sparse inflammatory cells and predominant hyaline membranes along alveolar septa with accentuation in alveolar ducts. In the organizing/proliferative phase, the hyaline membranes are incorporated into the alveolar septa through phagocytosis by macrophages or granulation tissue formation by proliferating myofibroblasts. Finally, the interstitium is thickened by loose myxoid fibroblastic tissue, causing altered pulmonary gas exchange mainly by diffusion impairment and ventilation-perfusion (V/Q) mismatch.
Acute respiratory failure etiologies and diagnostic work-up
In patients with ARF and ILD three possible scenarios have to be distinguished:
ARF in known chronic ILDs
The definition of AE-IPF has recently been revised as an acute (less than 1 month in duration) and clinically significant respiratory deterioration in a previously diagnosed IPF patient, associated with the presence of new widespread alveolar infiltrates on HRCT and exclusion of alternative etiologies (including infection, heart failure, pulmonary embolism, and, less frequently, pneumothorax, drug toxicity and diffuse alveolar hemorrhage - DAH -), . Questionably, this new definition removes the distinction between idiopathic and so-called triggered AE because considered irrelevant to patients’ outcome. Nevertheless, identifying the trigger of AE may influence patients’ management [58, 63].
AE may complicate the clinical course of other fibrosing ILDs, such as chronic hypersensitivity pneumonitis (CHP) [64,65,66], and non-specific interstitial pneumonia (NSIP) both idiopathic and secondary to CTD-ILD [61, 67,68,69]. The incidence of AE in CTD-ILDs depends on the underlying CTD (as an example, AE are more common in ILD secondary to Rheumatoid Arthritis) and AE may occur regardless of flares of the extrathoracic manifestations and in spite of the immunosuppressive treatment.
In clinical practice, a diagnostic work-up based on laboratory exams, CT scan (angioCT if pulmonary embolism is suspected), and bronchoscopy may be recommended in patients with ARF in a known ILD to evaluate all possible scenarios, Fig. 2.
Unknown chronic ILD presenting with ARF
Although less commonly than in a previously diagnosed ILD, ARF may also represent the clinical onset of an undiagnosed and unsuspected ILD. Possible ILDs presenting with this clinical manifestation are IPF, NSIP, CHP, CTD-ILDs, DAH and drug-toxicity [11, 13, 68, 70, 71].
In a previously apparently healthy patient presenting with ARF, the assessment of past medical history and symptoms, perhaps underestimated by the patient himself, is mandatory. Physical examination and laboratories (e.g. digital clubbing and polyglobulia) may reveal a long-standing respiratory failure or extrapulmonary manifestations of an underlying CTD or systemic vasculitis. However, the absence of extrapulmonary signs does not exclude an underlying CTD, as pulmonary manifestations may precede by months or years the more typical systemic manifestations, especially in rheumatoid arthritis, systemic lupus erythematosus, and polymyositis-dermatomyositis (lung-dominant ILD) . Therefore, complete autoimmune serology screening, inclusive of myositis-specific autoantibodies, might be helpful.
HRCT, performed as part of the initial assessment of ARF, should be carefully assessed to identify the presence of signs of architectural distortion such as traction bronchiectasis, lung volume loss and honeycombing, considered suggestive of a pre-existing ILD.
Bronchoscopy with bronchoalveolar lavage (BAL) and, in selected cases, lung biopsies may be useful in establishing the diagnosis of the underlying ILD. The indication for bronchoscopic assessment and the choice of the procedure to perform should be carefully discussed in each case, considering ARF severity, the potentially related complications and the risk to trigger an AE.
In unknown ILDs presenting with ARF and in de novo acute ILDs, as shown in the next section, the diagnostic work-up should always include both investigations on primary ILD (autoantibody panel and bronchoscopic procedures when respiratory gas exchange allows it) and investigations on concomitant conditions that may cause ARF, as summarised in Fig. 3.
De novo acute ILD presenting with ARF
ARF may also represent the clinical onset of a de novo rapidly progressive ILD. In the differential diagnosis the following should be considered: acute interstitial pneumonia (AIP), cryptogenic organizing pneumonia (COP), acute eosinophilic pneumonia (AEP), and drug-induced ILD , and, less frequently, acute hypersensitivity pneumonia, DAH in the setting of a de novo vasculitis, de novo CTD-ILD and lepidic adenocarcinoma with lymphangitic carcinomatosis.AIP, formerly known as Hamman-Rich syndrome, is a rare and fulminant form of diffuse lung injury with a clinical presentation similar to acute respiratory distress syndrome (ARDS), whose etiology remains uncertain . The in-hospital mortality rate is greater than 50% and the majority of patients who survive dies within six months of presentation [75, 76].
In 10–15% of cases, COP may present with a rapidly progressive course, mimicking ARDS . The diagnosis is made by ruling out infectious causes of pneumonia and documenting typical pathological changes in tissue obtained by lung biopsies demonstrating fibroblastic polyps, sometimes associated with endoalveolar fibrin deposits, the so-called acute fibrinous organizing pneumonia (AFOP). The majority of patients recovers completely with corticosteroid therapy but relapses are common [78, 79].
AEP occurs in previously healthy individuals and is characterized by pulmonary eosinophilia (more than 25% eosinophils on BAL differential cell count) or eosinophilic pneumonia on lung biopsy with or without peripheral eosinophilia .
Many chemotherapeutic (e.g. bleomycin and busulfan) and non-chemotherapeutic agents (e.g. amiodarone, nitrofurantoin, and statins) may cause lung toxicity manifesting with ARF. The diagnosis of a drug-induced acute ILD is challenging, and it is supported by the temporal relationship between the first use of the medication and symptoms onset, spontaneous clinical improvement after the discontinuation of the drug and recurrence of symptoms on re-challenge .
Although acute hypersensitivity pneumonitis is most commonly self-limited, it can also present with ARF. It should be suspected when there is a temporal association with the exposure to an inhaled antigen known to trigger hypersensitivity reactions, and in the presence of an upper-lobe predominant process accompanied by lymphocytic alveolitis [82, 83].
Diffuse alveolar haemorrhage presents with three possible histopathologic patterns: pulmonary capillaritis, most frequently encountered in granulomatosis with polyangiitis, bland pulmonary haemorrhage and DAD due to drugs or inhalation of toxic chemicals .
Possible diagnostic work-up for this presentation of ILDs is summarised in Fig. 3.
Initial evaluation of the severity of respiratory failure and how to choose the site and intensity of care
ARF represents a true clinical and ethical challenge, given the lack of benefit of IMV in the majority of patients with ARF and ILDs , the high susceptibility of these patients to ventilator-induced lung injury (VILI) [54, 85], and, subsequently, the high mortality rate of ILD patients in the ICU [86,87,88]. Despite the majority of studies having been conducted on AE-IPF [86, 87], it appears that AEs of non-IPF forms of ILD do not differ in terms of prognosis ; furthermore, the duration of the underlying ILD from diagnosis to ICU admission has not shown to correlate with mortality. The unique definitive treatment option for pharmacologically refractory advanced stage ILDs is lung transplant , and the decision to proceed to intensive life support measures in these patients cannot withstand the patient’s precedent enlisting. In rarer cases, a patient may be listed de novo upon ICU admission, in the form of a salvage transplant. To this aim, while waiting for lung transplant, IMV, and more recently ExtraCorporeal Membrane Oxygenation (ECMO) , have shown to be lifesaving options. Therefore, patients presenting with ARF on an underlying ILD should be addressed to centers specialized in ILD and disposing of a respiratory high dependency unit (HDU) and an ICU with ECMO experience; in case the patient is on the lung transplant list, he/she should be referred to the local transplant center [89, 91].
In respiratory HDUs, non-invasive ventilation (NIV) is effectively used to decrease work of breathing in patients such as those with exacerbation of chronic obstructive pulmonary disease (COPD). However, in most ILD cases with ARF the excessive work of breathing cannot be managed by NIV alone, and studies suggesting a definitive clinical benefit of NIV in ILDs are still lacking, as shown in the following sections of this review. Furthermore, a recent study on a large single-center cohort of NIV patients, showed that the presence of diffuse ILD was associated with increased mortality . In this scenario, NIV could have a role in selected patients, such as survivors from an AE-ILD, as a bridge to transplant [89, 93], or to reduce patient discomfort after the onset of ARF in those who are not candidate to lung transplant, while establishing other supportive measures . We will discuss specific indications and contraindications together with the available evidence in regards to various oxygenation and ventilation methods in the following sections.
Finally, given the poor prognosis, patients with end-stage ILD with no indication to transplant and aggressive life-support should not die in an acute care setting, but offered palliation and end-of-life supportive care . Furthermore, all patients in advanced stages of ILD that are not candidates to invasive treatments should receive appropriate counseling about the prognosis of the disease and the possible supportive measures available.
In conclusion, site of care in ILD patients with ARF may include a wide range of choices from an ICU with ECMO to palliation centers. Clinicians, with the support of a multidisciplinary team (e.g. pulmunologist and intensivist), should be prepared to promptly recognize a possible candidate to lung transplant from one who may benefit from comfort and supportive measures alone.
Acute respiratory failure treatment
Oxygen therapy and high-flow nasal cannula
Oxygen supplementation is the mainstay of treatment of ARF in ILDs. In the acute setting, different kinds of oxygen therapy are available, from simple nasal cannulae to face masks, including high concentration oxygen with reservoir mask and Venturi mask.
Patients with ILDs in advanced stages or during AE have a high degree of diffusion impairment and V/Q mismatch and require high oxygen concentrations to achieve satisfactory respiratory gas exchange. The risk of hypercapnia in these patients is usually minimal, and at the very end stages .
In some conditions, patients’ needs can be higher and the oxygen flows provided by conventional therapy may be lower than inspiratory peak flows. Humidified High-Flow Nasal Cannula (HFNC) oxygen therapy is a disposal, which may provide very high flows (up to 60 L/min) and utilizes an air oxygen blend allowing from 21 to 100% FIO2 delivery .
This modality of oxygen delivery may offer several advantages in comparison to the usual oxygen therapy, since it provides both steady FIO2, and, theoretically, an anatomical oxygen reservoir within the nasopharynx and oropharynx, by virtue of a carbon dioxide wash-out effect due to high oxygen flow [98,99,100,101]. This more efficient carbon dioxide elimination together with reduced dead space results in a reduced ventilatory drive that, ultimately, leads to a decreased respiratory rate and work of breathing [101, 102]. There is also a continuous positive airway pressure (CPAP) effect which provides an upper airway extending pressure that ranges between 3.2 and 7.4 cmH2O with the mouth closed and leads to an increased end-expiratory lung volume [103, 104]. Finally, the heated humidification facilitates secretion clearance, increasing patients’ comfort and maintaining mucosal integrity [105, 106]. Although there is increasing evidence in neonatal and paediatric settings , the utility of HFNC in ILDs is unknown.
A recent systematic review analyzed the effect of HFNC vs conventional oxygen therapy or NIV in adults including 11 randomised control trials (RCTs) and concluded that HFNC use was associated with reduction in intubation rate, need for IMV and rate of escalation of respiratory support when compared to conventional oxygen therapy . When HFNC was compared to NIV, no differences in the rate of intubation and escalation of respiratory support was observed. No difference was found in mortality between HFNC and conventional oxygen therapy or NIV utilization. However, inclusion criteria, as well as endpoints and etiology of ARF, were different among studies, leading to the impossibility to draw certain conclusions. In particular, none of the studies explicitly evaluated patients with ILDs.
No studies have yet assessed the effectiveness of HFNC in patients with ARF in ILD, with the exception of a case series. Horio et al. described three patients with AE of interstitial pneumonia and unsatisfactory respiratory gas exchange with no rebreathing face masks, who were successfully treated with HFNC .
In conclusion, HFNC in ILD patients might potentially be an alternative to conventional oxygen therapy in patients requiring both high concentration of oxygen and high-flow gas to correct hypoxemia and control dyspnea and tachypnea. However, the evidence is very scarce and RCTs are needed to establish the real efficacy of this oxygen delivery method.
The outcome of patients with ARF and ILDs ventilated in the ICU is very poor and IMV proved to be mostly futile . Current IPF guidelines recommend that the majority of patients with respiratory failure should not receive IMV . The reason of this finding lies in the fact that both the underlying structural lung disease and the precipitating condition causing ARF have a high likelihood of being irreversible and progressive. The pathogenic mechanisms causing AE-ILD have not yet been fully understood, thus, there are no treatments that have proven to be effective in RCTs. In this scenario, NIV may be applied in the hope to treat or stabilize the cause of ARF, minimizing complications and the poor outcome connected with endotracheal intubation (ETI) and IMV .
A few studies and case series have evaluated the application of NIV in ARF in ILDs. Two case series by Yokoyama and colleagues and Vianello et al. reported similar results in IPF patients with ARF [111, 112]. On one hand, a minority of patients benefited from NIV application (5/11–45% - and 8/18–44%, in the cohorts of Yokoyama and Vianello, respectively), and, in those who responded, the use of NIV was associated with better outcomes, including avoidance of ETI and better survival. On the other hand, patients who failed NIV died within 3 months, regardless of ETI.
Gungor and colleagues evaluated the use of NIV both in IPF and in other ILDs with better overall prognosis, including CTD and silicosis , however, they found similar outcomes to the previously cited cohorts of IPF patients [111, 112], with a higher mortality rate and NIV failure in those who needed continuous NIV compared to those that were able to tolerate NIV interruptions for feeding.
NIV responsiveness was associated with less severe ARF and patients’ condition in most series [94, 111,112,113,114]. Furthermore, Yokoyama et al. in a study on 38 patients with ARF in ILDs, including IPF, CTD-ILD and drug-induced ILD, reported that early NIV initiation during the acute phase was associated with better 30-day survival , indicating that early optimization of supportive care, including oxygenation, may improve patients’ management and short-term outcomes.
A further step was attempted by Aliberti and colleagues who evaluated NIV responsiveness in patients with ILD and ARF in a multicentre study, stratifying the results according to the cause of ARF and the underlying radiological pattern of ILD . NIV showed to improve oxygenation in patients with pneumonia, but not in those with AE; however, this positive effect on oxygenation did not translate into improved outcomes in patients with pneumonia compared to those with AE. No differences were observed in terms of radiological pattern. These results seem to suggest that, in spite of a better oxygenation in specific subgroups of patients, NIV outcomes do not depend on the radiological pattern or underlying cause of ARF. In fact, even if the precipitating factors are promptly recognized and treated, most cases show an irreversible deterioration of baseline conditions.
In conclusion, despite the high rate of NIV failure in patients with ARF in ILDs, in selected patients, such as those with less severe respiratory failure, an early NIV trial might facilitate the recognition of NIV-responder patients, who may present better short-term clinical outcomes. However, NIV responsiveness does not seem to impact on the poor prognosis related to the underlying disease: one-year mortality rate in NIV-responder patients was ≥70% in all the studies evaluated [94, 111, 112].
The main difficulties encountered when applying NIV on patients with ILDs and some practical tips to overcome them are summarised in Table 2.
Invasive mechanical ventilation
During an episode of severe ARF, patients might need intensive care support, including ETI and IMV. Multiple retrospective studies have taken into account patients with IPF admitted to the ICU for ARF [11, 54, 55, 86, 87, 116, 117]. In all the reported studies, IMV was associated with negative clinical outcomes, in some cases with an in-hospital mortality higher than 90%. In some cohorts causes of ARF were divided into reversible, such as pneumonia, and irreversible, mainly AE-ILD. In the absence of reversible causes, patients did not seem to benefit from IMV, and, in these cases, some authors advised against the use of IMV, with the exception of patients listed for lung transplant .
A study by Mollica et al. in 2010 compared IMV to NIV or spontaneous breathing in patients with ARF and IPF . Although both ventilatory strategies improved PaO2/FIO2 ratio, in comparison to spontaneous breathing, the authors reported a global in-hospital mortality of 85%, that rose up to 100% in patients treated with IMV.
Other authors evaluated the use of IMV in ARF in non-IPF fibrotic ILDs. Molina-Molina et al. assessed 20 patients with fibrotic ILDs (14 with IPF and 6 with CTD-ILD) who required IMV : similarly to cohorts with only IPF patients, IMV was associated with 100% in-hospital mortality.
Vincent et al. and Gaudry and colleagues, described the same scenario from a different point of view [119, 120]. Both authors described IPF and fibrotic-NSIP patients with ARF treated with NIV or IMV. Vincent et al. observed that by dividing their cases into two successive time periods (the first period from 1999 to 2004 and the second from 2005 to 2009), the patient’s prognosis improved in the second time period compared to the first . Despite all the limitations of this study, the authors hypothesized that some of the improvements introduced in the years, including lung-protective ventilatory parameters with lower tidal volumes and plateau pressures and earlier admission to the ICU, might have changed the outcomes of these patients, suggesting that not all patients are doomed to poor short-term outcomes. Gaudry et al., while observing a poor prognosis in most cases (21 out of 27 patients, 85%, died during hospitalization), found that a small subgroup of patients survived (6 cases) and some of them were able to reach pulmonary transplant (2 patients, 7%), confirming that IMV might be indicated in very selected patients candidate to lung transplant .
One of the mechanisms involved in the poor prognosis of mechanically ventilated patients with advanced fibrotic ILDs is VILI [88, 120]. The forces applied through IMV can cause pathophysiological alterations culminating in the disruption of cell membranes and cell-cell contacts, particularly in those patients with inhomogeneously injured lungs, such as in ARDS . The fibrotic lung might be subject to a similar VILI as a consequence of baro- and volutrauma. Nava and colleagues assessed the respiratory mechanics of end-stage fibrotic ILDs during IMV and reported an approximately fourfold increase in the elastance of the respiratory system compared to normal anaesthetised subjects ; the values reported were even higher than those in patients with ARDS . This marked increase in lung elastance is mainly due to the “stiffness” of the fibrotic lung. At the same time, the authors also observed that the resistance of the respiratory system was markedly increased compared with the values reported for normal subjects (although to a lesser extent than COPD patients) . This finding reflects similar observations by West and colleagues that reported in patients with fibrotic lung diseases an increased resistive work in association with a higher work of breathing in comparison to normal subjects .
In conclusion, despite the low quality of the evidence available, IMV in patients with IPF and advanced fibrotic ILDs that develop ARF seems to be contraindicated, because of the high short-term mortality. However, it is necessary to differentiate some subgroups of patients, such as those with a potentially reversible cause of ARF or those listed for lung transplant, on whom prognostic data are less accurate and indications to IMV should be assessed on a case-by-case basis.
Extracorporeal membrane oxygenation
ECMO, referring to an extracorporeal circuit that directly oxygenates and removes carbon dioxide from the blood, may be considered in refractory severe ARF when positive-pressure ventilation, in combination with other ventilatory strategies such as prone positioning and neuromuscular block, results in unacceptable levels of hypoxemia, hypercapnia and acidemia .
ECMO in ILDs might be considered in patients with severe respiratory failure secondary to a potentially reversible cause of deterioration (e.g., infection or pulmonary embolism) and if the patient is a candidate for lung transplant .
The recent improvements in ECMO technology have allowed some centres to use less invasive ECMO or other extracorporeal devices to liberate patients from IMV and successfully bridge them to lung transplantation .
Trudzinski et al. reported their experience with ILD patients treated with ECMO for ARF . ECMO was only used when patients were considered potential candidates for lung transplant or when two intensivists agreed on a potentially reversible pulmonary cause of ARF (e.g., acute infection on previous chronic ILD). Indications for veno-venous ECMO in the 21 patients included in the study were: refractory hypoxemia or uncompensated hypercapnia in ARDS despite optimization of IMV, or refractory hypoxemia despite maximal non-invasive therapies in patients considered “at risk of intubation”. In the latter case, ECMO was used to prevent intubation, and referred to as “awake-ECMO”, meaning the use of ECMO in awake, non-intubated, spontaneously breathing patients. The authors reported that out of the 21 patients treated with ECMO, six (29%) underwent lung transplant and two (10%) died on the waiting list after 9 and 63 days on ECMO. Of the 15 patients who did not undergo lung transplantation, 14 died after a mean time on ECMO of 40 days. These results confirm that in the absence of effective therapeutic perspectives (e.g. transplantation), ECMO is unable to prevent the irreversible progression of the underlying disease and does not improve mortality in patients with severe ARF and ILDs.
Fuehner et al. were the first to compare the outcomes of awake-ECMO patients with terminal respiratory or cardiopulmonary failure candidate to lung transplant to a historical cohort of patients treated with conventional IMV as bridge to transplant . The duration of awake-ECMO and IMV were similar between the 2 groups (median 9 and 15 days, respectively), as well as the mortality rate on ECMO and IMV before a donor organ was available (23 and 29%, respectively). Results were encouraging, with a 6-month survival rate after transplantation of 80% in the “awake-ECMO” group vs 50% in the mechanically ventilated group.
A strategy based on ECMO to avoid IMV might potentially offer numerous benefits, including prevention of VILI and ventilator-associated pneumonia, preservation of oral feeding, spontaneous coughing, and social interaction, and allowance of early rehabilitation . However, extracorporeal support devices are frequently linked to complications, including vessel perforation, bleeding, and infections. The main complications reported in Trudzinski’s cohort were bleeding (3 cases, 14%) and cannulation placement (2 cases, 13%), while in Fuehner’s cohort were bleeding requiring transfusions (8 cases, 31%), sepsis-like syndrome (5 cases, 19%), intractable coughing requiring ETI (2 cases, 8%).
Of all the available forms of extracorporeal gas exchange, partial lung support, also known as extracorporeal CO2 removal (ECCO2R) or respiratory dialysis, has shown some interesting results . Recently, ECCO2R has been proposed as an intervention to eliminate CO2 from the blood of patients undergoing NIV who are unable to achieve adequate gas exchange despite optimization of ventilatory settings . Vianello et al. described the successful management of an IPF patient with ARF using a pump-assisted veno-venous system for ECCO2R as an alternative to ETI following NIV failure . The authors were able to minimize the complications most commonly related to ECMO by using a small single veno-venous dual lumen catheter. However, both clinicians’ experience and the technology behind ECCO2R still need to be improved before its use can be widely implemented in clinical practice.
In conclusion, extracorporeal lung support might allow to prevent or reduce the invasiveness of IMV, and, therefore, minimize the risk of “triggering” fatal deterioration of the underlying chronic process, such as VILI. However, ECMO alone does not change the poor outcome associated with severe ARF in ILDs, and, given the high costs and risk of complications, should be limited to patients with a potential good short-term prognosis, e.g. those listed for lung transplant.
ARF is a feared complication in ILDs, both for its difficult management and diagnostic work-up and the poor prognosis.
Oxygen supplementation and ventilatory support have proven to be ineffective in modifying the prognosis of the disease in the absence of effective therapeutic options. Less invasive techniques, including HFNC oxygen and NIV, might be used in less severe cases to correct hypoxemia and control dyspnea, while, invasive techniques, such as IMV and ECMO, should be limited to patients listed for lung transplant or with reversible causes of ARF.
AE of IPF
Acute eosinophilic pneumonia
Acute fibrinous organizing pneumonia
Acute interstitial pneumonia
Acute respiratory distress syndrome
Acute respiratory failure
Chronic hypersensitivity pneumonitis
Cryptogenic organizing pneumonia
Chronic obstructive pulmonary disease
Continuous positive airway pressure
Connective tissue disease related ILD
Diffuse alveolar damage
Diffuse alveolar hemorrhage
Extracorporeal CO2 removal
ExtraCorporeal Membrane Oxygenation
High dependency unit
High-Flow Nasal Cannula
High-resolution computed tomography
Intensive care unit
Interstitial lung disease
Invasive mechanical ventilation
Idiopathic pulmonary fibrosis
Non-specific interstitial pneumonia
Randomised control trial
Ventilator-induced lung injury
Ryerson CJ, Collard HR. Update on the diagnosis and classification of ILD. Curr Opin Pulm Med. 2013;19:453–9.
Travis WD, Costabel U, Hansell DM, King TE, Lynch DA, Nicholson AG, et al. An official American Thoracic Society/European Respiratory Society statement: update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med. 2013;188:733–48.
Coultas DB, Zumwalt RE, Black WC, Sobonya RE. The epidemiology of interstitial lung diseases. Am J Respir Crit Care Med. 1994;150:967–72.
Kaunisto J, Salomaa E-R, Hodgson U, Kaarteenaho R, Myllärniemi M. Idiopathic pulmonary fibrosis--a systematic review on methodology for the collection of epidemiological data. Bmc Pulm Med. 2013;13:53.
Nalysnyk L, Cid-Ruzafa J, Rotella P, Esser D. Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature. Eur Respir Rev Off J Eur Respir Soc. 2012;21:355–61.
Azuma A, Nukiwa T, Tsuboi E, Suga M, Abe S, Nakata K, et al. Double-blind, placebo-controlled trial of pirfenidone in patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2005;171:1040–7.
Noble PW, Albera C, Bradford WZ, Costabel U, Glassberg MK, Kardatzke D, et al. Pirfenidone in patients with idiopathic pulmonary fibrosis (CAPACITY): two randomised trials. Lancet Lond. Engl. 2011;377:1760–9.
Daniels CE, Lasky JA, Limper AH, Mieras K, Gabor E, Schroeder DR, et al. Imatinib treatment for idiopathic pulmonary fibrosis: randomized placebo-controlled trial results. Am J Respir Crit Care Med. 2010;181:604–10.
Kubo H, Nakayama K, Yanai M, Suzuki T, Yamaya M, Watanabe M, et al. Anticoagulant therapy for idiopathic pulmonary fibrosis. Chest. 2005;128:1475–82.
Demedts M, Behr J, Buhl R, Costabel U, Dekhuijzen R, Jansen HM, et al. High-dose acetylcysteine in idiopathic pulmonary fibrosis. N Engl J Med. 2005;353:2229–42.
Kim DS, Park JH, Park BK, Lee JS, Nicholson AG, Colby T. Acute exacerbation of idiopathic pulmonary fibrosis: frequency and clinical features. Eur Respir J. 2006;27:143–50.
Kishaba T, Tamaki H, Shimaoka Y, Fukuyama H, Yamashiro S. Staging of acute exacerbation in patients with idiopathic pulmonary fibrosis. Lung. 2014;192:141–9.
Song JW, Hong S-B, Lim C-M, Koh Y, Kim DS. Acute exacerbation of idiopathic pulmonary fibrosis: incidence, risk factors and outcome. Eur Respir J. 2011;37:356–63.
Taniguchi H, Ebina M, Kondoh Y, Ogura T, Azuma A, Suga M, et al. Pirfenidone in idiopathic pulmonary fibrosis. Eur Respir J. 2010;35:821–9.
Idiopathic Pulmonary Fibrosis Clinical Research Network, Martinez FJ, de Andrade JA, Anstrom KJ, King TE, Raghu G. Randomized trial of acetylcysteine in idiopathic pulmonary fibrosis. N Engl J Med. 2014;370:2093–101.
Richeldi L, Costabel U, Selman M, Kim DS, Hansell DM, Nicholson AG, et al. Efficacy of a tyrosine kinase inhibitor in idiopathic pulmonary fibrosis. N Engl J Med. 2011;365:1079–87.
Richeldi L, du Bois RM, Raghu G, Azuma A, Brown KK, Costabel U, et al. Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis. N Engl J Med. 2014;370:2071–82.
King TE, Albera C, Bradford WZ, Costabel U, Hormel P, Lancaster L, et al. Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (INSPIRE): a multicentre, randomised, placebo-controlled trial. Lancet Lond Engl. 2009;374:222–8.
King TE, Bradford WZ, Castro-Bernardini S, Fagan EA, Glaspole I, Glassberg MK, et al. A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis. N Engl J Med. 2014;370:2083–92.
King TE, Brown KK, Raghu G, du Bois RM, Lynch DA, Martinez F, et al. BUILD-3: a randomized, controlled trial of bosentan in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2011;184:92–9.
King TE, Behr J, Brown KK, du Bois RM, Lancaster L, de Andrade JA, et al. BUILD-1: a randomized placebo-controlled trial of bosentan in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2008;177:75–81.
Raghu G, Behr J, Brown KK, Egan JJ, Kawut SM, Flaherty KR, et al. Treatment of idiopathic pulmonary fibrosis with ambrisentan: a parallel, randomized trial. Ann Intern Med. 2013;158(9):641.
Noth I, Anstrom KJ, Calvert SB, de Andrade J, Flaherty KR, Glazer C, et al. A placebo-controlled randomized trial of warfarin in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2012;186:88–95.
Kondoh Y, Taniguchi H, Katsuta T, Kataoka K, Kimura T, Nishiyama O, et al. Risk factors of acute exacerbation of idiopathic pulmonary fibrosis. Sarcoidosis Vasc Diffuse Lung Dis Off J Wasog. 2010;27:103–10.
Idiopathic Pulmonary Fibrosis Clinical Research Network, Zisman DA, Schwarz M, Anstrom KJ, Collard HR, Flaherty KR, et al. A controlled trial of sildenafil in advanced idiopathic pulmonary fibrosis. N Engl J Med. 2010;363:620–8.
Idiopathic Pulmonary Fibrosis Clinical Research Network, Raghu G, Anstrom KJ, King TE, Lasky JA, Martinez FJ. Prednisone, azathioprine, and N-acetylcysteine for pulmonary fibrosis. N Engl J Med. 2012;366:1968–77.
Collard HR, Yow E, Richeldi L, Anstrom KJ, Glazer C, investigators IPF. Suspected acute exacerbation of idiopathic pulmonary fibrosis as an outcome measure in clinical trials. Respir Res. 2013;14:73.
Suzuki H, Sekine Y, Yoshida S, Suzuki M, Shibuya K, Yonemori Y, et al. Risk of acute exacerbation of interstitial pneumonia after pulmonary resection for lung cancer in patients with idiopathic pulmonary fibrosis based on preoperative high-resolution computed tomography. Surg Today. 2011;41:914–21.
Shintani Y, Ohta M, Iwasaki T, Ikeda N, Tomita E, Kawahara K, et al. Predictive factors for postoperative acute exacerbation of interstitial pneumonia combined with lung cancer. Gen Thorac Cardiovasc Surg. 2010;58:182–5.
Collard HR, Ryerson CJ, Corte TJ, Jenkins G, Kondoh Y, Lederer DJ, et al. Acute exacerbation of idiopathic pulmonary fibrosis. An international working group report. Am J Respir Crit Care Med. 2016;194:265–75.
Kondoh Y, Taniguchi H, Ebina M, Azuma A, Ogura T, Taguchi Y, et al. Risk factors for acute exacerbation of idiopathic pulmonary fibrosis--extended analysis of pirfenidone trial in Japan. Respir. Investig. 2015;53:271–8.
Costabel U, Inoue Y, Richeldi L, Collard HR, Tschoepe I, Stowasser S, et al. Efficacy of Nintedanib in idiopathic pulmonary fibrosis across Prespecified subgroups in INPULSIS. Am J Respir Crit Care Med. 2016;193:178–85.
Akira M, Kozuka T, Yamamoto S, Sakatani M. Computed tomography findings in acute exacerbation of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2008;178:372–8.
Lee JS, Collard HR, Anstrom KJ, Martinez FJ, Noth I, Roberts RS, et al. Anti-acid treatment and disease progression in idiopathic pulmonary fibrosis: an analysis of data from three randomised controlled trials. Lancet Respir Med. 2013;1:369–76.
Lee JS, Song JW, Wolters PJ, Elicker BM, King TE, Kim DS, et al. Bronchoalveolar lavage pepsin in acute exacerbation of idiopathic pulmonary fibrosis. Eur Respir J. 2012;39:352–8.
Johannson KA, Vittinghoff E, Lee K, Balmes JR, Ji W, Kaplan GG, et al. Acute exacerbation of idiopathic pulmonary fibrosis associated with air pollution exposure. Eur Respir J. 2014;43:1124–31.
Spagnolo P, Cottin V. Genetics of idiopathic pulmonary fibrosis: from mechanistic pathways to personalised medicine. J Med Genet. 2017;54:93–9.
Sakamoto K, Taniguchi H, Kondoh Y, Wakai K, Kimura T, Kataoka K, et al. Acute exacerbation of IPF following diagnostic bronchoalveolar lavage procedures. Respir Med. 2012;106:436–42.
Bando M, Ohno S, Hosono T, Yanase K, Sato Y, Sohara Y, et al. Risk of acute exacerbation after video-assisted Thoracoscopic lung biopsy for interstitial lung disease. J Bronchology Interv Pulmonol. 2009;16:229–35.
Sakamoto S, Homma S, Mun M, Fujii T, Kurosaki A, Yoshimura K. Acute exacerbation of idiopathic interstitial pneumonia following lung surgery in 3 of 68 consecutive patients: a retrospective study. Intern. Med. Tokyo Jpn. 2011;50:77–85.
Mizuno Y, Iwata H, Shirahashi K, Takamochi K, Oh S, Suzuki K, et al. The importance of intraoperative fluid balance for the prevention of postoperative acute exacerbation of idiopathic pulmonary fibrosis after pulmonary resection for primary lung cancer. Eur J Cardio-Thorac Surg Off J Eur Assoc Cardio-Thorac Surg. 2012;41:e161–5.
Kenmotsu H, Naito T, Kimura M, Ono A, Shukuya T, Nakamura Y, et al. The risk of cytotoxic chemotherapy-related exacerbation of interstitial lung disease with lung cancer. J Thorac Oncol Off Publ Int Assoc Study Lung Cancer. 2011;6:1242–6.
Takeda A, Enomoto T, Sanuki N, Nakajima T, Takeda T, Sayama K, et al. Acute exacerbation of subclinical idiopathic pulmonary fibrosis triggered by hypofractionated stereotactic body radiotherapy in a patient with primary lung cancer and slightly focal honeycombing. Radiat Med. 2008;26:504–7.
Ohshimo S, Ishikawa N, Horimasu Y, Hattori N, Hirohashi N, Tanigawa K, et al. Baseline KL-6 predicts increased risk for acute exacerbation of idiopathic pulmonary fibrosis. Respir Med. 2014;108:1031–9.
Kishaba T, Shimaoka Y, Fukuyama H, Yoshida K, Tanaka M, Yamashiro S, et al. A cohort study of mortality predictors and characteristics of patients with combined pulmonary fibrosis and emphysema. BMJ Open. 2012;2
Raghu G, Rochwerg B, Zhang Y, Garcia CAC, Azuma A, Behr J, et al. An official ATS/ERS/JRS/ALAT clinical practice guideline: treatment of idiopathic pulmonary fibrosis. An update of the 2011 clinical practice guideline. Am J Respir Crit Care Med. 2015;192:e3–19.
Olson AL, Swigris JJ, Lezotte DC, Norris JM, Wilson CG, Brown KK. Mortality from pulmonary fibrosis increased in the United States from 1992 to 2003. Am J Respir Crit Care Med. 2007;176:277–84.
Natsuizaka M, Chiba H, Kuronuma K, Otsuka M, Kudo K, Mori M, et al. Epidemiologic survey of Japanese patients with idiopathic pulmonary fibrosis and investigation of ethnic differences. Am J Respir Crit Care Med. 2014;190:773–9.
Daniels CE, Yi ES, Ryu JH. Autopsy findings in 42 consecutive patients with idiopathic pulmonary fibrosis. Eur Respir J. 2008;32:170–4.
Agarwal R, Jindal SK. Acute exacerbation of idiopathic pulmonary fibrosis: a systematic review. Eur J Intern Med. 2008;19:227–35.
Huie TJ, Olson AL, Cosgrove GP, Janssen WJ, Lara AR, Lynch DA, et al. A detailed evaluation of acute respiratory decline in patients with fibrotic lung disease: aetiology and outcomes. Respirol Carlton Vic. 2010;15:909–17.
Tachibana K, Inoue Y, Nishiyama A, Sugimoto C, Matsumuro A, Hirose M, et al. Polymyxin-B hemoperfusion for acute exacerbation of idiopathic pulmonary fibrosis: serum IL-7 as a prognostic marker. Sarcoidosis Vasc. Diffuse lung dis. Off. J Wasog. 2011;28:113–22.
Simon-Blancal V, Freynet O, Nunes H, Bouvry D, Naggara N, Brillet P-Y, et al. Acute exacerbation of idiopathic pulmonary fibrosis: outcome and prognostic factors. Respir. Int. Rev. Thorac. Dis. 2012;83:28–35.
Rangappa P, Moran JL. Outcomes of patients admitted to the intensive care unit with idiopathic pulmonary fibrosis. Crit. Care Resusc. J. Australas. Acad. Crit Care Med. 2009;11:102–9.
Al-Hameed FM, Sharma S. Outcome of patients admitted to the intensive care unit for acute exacerbation of idiopathic pulmonary fibrosis. Can Respir J. 2004;11:117–22.
Navaratnam V, Ali N, Smith CJP, McKeever T, Fogarty A, Hubbard RB. Does the presence of connective tissue disease modify survival in patients with pulmonary fibrosis? Respir Med. 2011;105:1925–30.
Thomeer MJ, Vansteenkiste J, Verbeken EK, Demedts M. Interstitial lung diseases: characteristics at diagnosis and mortality risk assessment. Respir Med. 2004;98:567–73.
Moua T, Westerly BD, Dulohery MM, Daniels CE, Ryu JH, Lim KG. Patients with fibrotic interstitial lung disease hospitalized for acute respiratory worsening: a large cohort analysis. Chest. 2016;149:1205–14.
Ambrosini V, Cancellieri A, Chilosi M, Zompatori M, Trisolini R, Saragoni L, et al. Acute exacerbation of idiopathic pulmonary fibrosis: report of a series. Eur Respir J. 2003;22:821–6.
Collard HR, Moore BB, Flaherty KR, Brown KK, Kaner RJ, King TE, et al. Acute exacerbations of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2007;176:636–43.
Rice AJ, Wells AU, Bouros D, du Bois RM, Hansell DM, Polychronopoulos V, et al. Terminal diffuse alveolar damage in relation to interstitial pneumonias. An autopsy study Am J Clin Pathol. 2003;119:709–14.
Rush B, Wiskar K, Berger L, Griesdale D. The use of mechanical ventilation in patients with idiopathic pulmonary fibrosis in the United States: a nationwide retrospective cohort analysis. Respir Med. 2016;111:72–6.
Huie TJ, Olson AL, Cosgrove GP, Janssen WJ, Lara AR, Lynch DA, et al. A detailed evaluation of acute respiratory decline in patients with fibrotic lung disease: aetiology and outcomes. Respirol. Carlton Vic. 2010;15:909–17.
Churg A, Müller NL, Silva CIS, Wright JL. Acute exacerbation (acute lung injury of unknown cause) in UIP and other forms of fibrotic interstitial pneumonias. Am J Surg Pathol. 2007;31:277–84.
Olson AL, Huie TJ, Groshong SD, Cosgrove GP, Janssen WJ, Schwarz MI, et al. Acute exacerbations of fibrotic hypersensitivity pneumonitis: a case series. Chest. 2008;134:844–50.
Miyazaki Y, Tateishi T, Akashi T, Ohtani Y, Inase N, Yoshizawa Y. Clinical predictors and histologic appearance of acute exacerbations in chronic hypersensitivity pneumonitis. Chest. 2008;134:1265–70.
Suda T, Kaida Y, Nakamura Y, Enomoto N, Fujisawa T, Imokawa S, et al. Acute exacerbation of interstitial pneumonia associated with collagen vascular diseases. Respir Med. 2009;103:846–53.
Spagnolo P, Wuyts W. Acute exacerbations of interstitial lung disease: lessons from idiopathic pulmonary fibrosis. Curr Opin Pulm Med. 2017;23:411–7.
Park I-N, Kim DS, Shim TS, Lim C-M, Lee SD, Koh Y, et al. Acute exacerbation of interstitial pneumonia other than idiopathic pulmonary fibrosis. Chest. 2007;132:214–20.
Parambil JG, Myers JL, Ryu JH. Histopathologic features and outcome of patients with acute exacerbation of idiopathic pulmonary fibrosis undergoing surgical lung biopsy. Chest. 2005;128(5):3310.
Douglas WW, Tazelaar HD, Hartman TE, Hartman RP, Decker PA, Schroeder DR, et al. Polymyositis-dermatomyositis-associated interstitial lung disease. Am J Respir Crit Care Med. 2001;164:1182–5.
Tzelepis GE, Toya SP, Moutsopoulos HM. Occult connective tissue diseases mimicking idiopathic interstitial pneumonias. Eur Respir J. 2008;31:11–20.
Taniguchi H, Kondoh Y. Acute and subacute idiopathic interstitial pneumonias. Respirol. Carlton Vic. 2016;21:810–20.
Olson J, Colby TV, Elliott CG. Hamman-rich syndrome revisited. Mayo Clin Proc. 1990;65:1538–48.
Bouros D, Nicholson AC, Polychronopoulos V, du Bois RM. Acute interstitial pneumonia. Eur Respir J. 2000;15:412–8.
Vourlekis JS, Brown KK, Cool CD, Young DA, Cherniack RM, King TE, et al. Acute interstitial pneumonitis. Case series and review of the literature. Medicine (Baltimore). 2000;79:369–78.
Cohen AJ, King TE, Downey GP. Rapidly progressive bronchiolitis obliterans with organizing pneumonia. Am J Respir Crit Care Med. 1994;149:1670–5.
King TE, Mortenson RL. Cryptogenic organizing pneumonitis. The north American experience. Chest 1992;102:8S–13S.
Oymak FS, Demirbaş HM, Mavili E, Akgun H, Gulmez I, Demir R, et al. Bronchiolitis obliterans organizing pneumonia. Clinical and roentgenological features in 26 cases. Respir. Int. Rev. Thorac. Dis. 2005;72:254–62.
Philit F, Etienne-Mastroïanni B, Parrot A, Guérin C, Robert D, Cordier J-F. Idiopathic acute eosinophilic pneumonia: a study of 22 patients. Am J Respir Crit Care Med. 2002;166(9):1235.
Camus P, Bonniaud P, Fanton A, Camus C, Baudaun N, Foucher P. Drug-induced and iatrogenic infiltrative lung disease. Clin Chest Med. 2004;25:479–519. vi
Patel AM, Ryu JH, Reed CE. Hypersensitivity pneumonitis: current concepts and future questions. J Allergy Clin Immunol. 2001;108:661–70.
D’Ippolito R, Chetta A, Foresi A, Marangio E, Castagnaro A, Merliniaft S, et al. Induced sputum and bronchoalveolar lavage from patients with hypersensitivity pneumonitis. Respir Med. 2004;98:977–83.
Imoto EM, Lombard CM, Sachs DP. Pulmonary capillaritis and hemorrhage. A clue to the diagnosis of systemic necrotizing vasculitis. Chest. 1989;96:927–8.
Mallick S. Outcome of patients with idiopathic pulmonary fibrosis (IPF) ventilated in intensive care unit. Respir Med. 2008;102:1355–9.
Blivet S, Philit F, Sab JM, Langevin B, Paret M, Guérin C, et al. Outcome of patients with idiopathic pulmonary fibrosis admitted to the ICU for respiratory failure. Chest. 2001;120:209–12.
Saydain G, Islam A, Afessa B, Ryu JH, Scott JP, Peters SG. Outcome of patients with idiopathic pulmonary fibrosis admitted to the intensive care unit. Am J Respir Crit Care Med. 2002;166:839–42.
Fernández-Pérez ER, Yilmaz M, Jenad H, Daniels CE, Ryu JH, Hubmayr RD, et al. Ventilator settings and outcome of respiratory failure in chronic interstitial lung disease. Chest. 2008;133:1113–9.
Papiris SA, Manali ED, Kolilekas L, Kagouridis K, Triantafillidou C, Tsangaris I, et al. Clinical review: idiopathic pulmonary fibrosis acute exacerbations--unravelling Ariadne’s thread. Crit. Care Lond. Engl. 2010;14:246.
Trudzinski FC, Kaestner F, Schäfers H-J, Fähndrich S, Seiler F, Böhmer P, et al. Outcome of patients with interstitial lung disease treated with extracorporeal membrane oxygenation for acute respiratory failure. Am J Respir Crit Care Med. 2016;193:527–33.
Bradley B, Branley HM, Egan JJ, Greaves MS, Hansell DM, Harrison NK, et al. Interstitial lung disease guideline: the British Thoracic Society in collaboration with the Thoracic Society of Australia and new Zealand and the Irish thoracic society. Thorax. 2008;63(Suppl 5):v1–58.
Gacouin A, Jouneau S, Letheulle J, Kerjouan M, Bouju P, Fillatre P, et al. Trends in prevalence and prognosis in subjects with acute chronic respiratory failure treated with noninvasive and/or invasive ventilation. Respir Care. 2015;60:210–8.
Trulock EP, Edwards LB, Taylor DO, Boucek MM, Mohacsi PJ, Keck BM, et al. The registry of the International Society for Heart and Lung Transplantation: twentieth official adult lung and heart-lung transplant report--2003. J. Heart lung transplant. Off. Publ. Int. Soc. Heart Transplant. 2003;22:625–35.
Mollica C, Paone G, Conti V, Ceccarelli D, Schmid G, Mattia P, et al. Mechanical ventilation in patients with end-stage idiopathic pulmonary fibrosis. Respiration. 2010;79:209–15.
Rajala K, Lehto JT, Saarinen M, Sutinen E, Saarto T, Myllärniemi M. End-of-life care of patients with idiopathic pulmonary fibrosis. Bmc Palliat Care. 2016;15:85.
O’Driscoll BR, Howard LS, Davison AG. British Thoracic Society. BTS guideline for emergency oxygen use in adult patients. Thorax. 2008;63(Suppl 6):vi1–68.
Spoletini G, Alotaibi M, Blasi F, Hill NS. Heated humidified high-flow nasal oxygen in adults: mechanisms of action and clinical implications. Chest. 2015;148:253–61.
Parke R, McGuinness S, Eccleston M. Nasal high-flow therapy delivers low level positive airway pressure. Br J Anaesth. 2009;103:886–90.
Ritchie JE, Williams AB, Gerard C, Hockey H. Evaluation of a humidified nasal high-flow oxygen system, using oxygraphy, capnography and measurement of upper airway pressures. Anaesth Intensive Care. 2011;39:1103–10.
Schreiber A, DI Marco F, Braido F, Solidoro P. High flow nasal cannula oxygen therapy, work in progress in respiratory critical care. Minerva Med. 2016;107:14–20.
Bräunlich J, Beyer D, Mai D, Hammerschmidt S, Seyfarth H-J, Wirtz H. Effects of nasal high flow on ventilation in volunteers, COPD and idiopathic pulmonary fibrosis patients. Respir Int Rev Thorac Dis. 2013;85:319–25.
Schwabbauer N, Berg B, Blumenstock G, Haap M, Hetzel J, Riessen R. Nasal high-flow oxygen therapy in patients with hypoxic respiratory failure: effect on functional and subjective respiratory parameters compared to conventional oxygen therapy and non-invasive ventilation (NIV). Bmc Anesth. 2014;14:66.
Chanques G, Riboulet F, Molinari N, Carr J, Jung B, Prades A, et al. Comparison of three high flow oxygen therapy delivery devices: a clinical physiological cross-over study. Minerva Anestesiol. 2013;79:1344–55.
Ward JJ. High-flow oxygen administration by nasal cannula for adult and perinatal patients. Respir Care. 2013;58:98–122.
Williams R, Rankin N, Smith T, Galler D, Seakins P. Relationship between the humidity and temperature of inspired gas and the function of the airway mucosa. Crit Care Med. 1996;24:1920–9.
Sztrymf B, Messika J, Bertrand F, Hurel D, Leon R, Dreyfuss D, et al. Beneficial effects of humidified high flow nasal oxygen in critical care patients: a prospective pilot study. Intensive Care Med. 2011;37:1780–6.
Wilkinson D, Andersen C, O’Donnell CPF, De Paoli AG, Manley BJ. High flow nasal cannula for respiratory support in preterm infants. Cochrane Database Syst Rev. 2016;2:CD006405.
Zhao H, Wang H, Sun F, Lyu S, An Y. High-flow nasal cannula oxygen therapy is superior to conventional oxygen therapy but not to noninvasive mechanical ventilation on intubation rate: a systematic review and meta-analysis. Crit Care Lond Engl. 2017;21:184.
Horio Y, Takihara T, Niimi K, Komatsu M, Sato M, Tanaka J, et al. High-flow nasal cannula oxygen therapy for acute exacerbation of interstitial pneumonia: a case series. Respir Investig. 2016;54:125–9.
Tomii K, Tachikawa R, Chin K, Murase K, Handa T, Mishima M, et al. Role of non-invasive ventilation in managing life-threatening acute exacerbation of interstitial pneumonia. Intern. Med. Tokyo Jpn. 2010;49:1341–7.
Yokoyama T, Kondoh Y, Taniguchi H, Kataoka K, Kato K, Nishiyama O, et al. Noninvasive ventilation in acute exacerbation of idiopathic pulmonary fibrosis. Intern Med. 2010;49:1509–14.
Vianello A, Arcaro G, Battistella L, Pipitone E, Vio S, Concas A, et al. Noninvasive ventilation in the event of acute respiratory failure in patients with idiopathic pulmonary fibrosis. J Crit Care. 2014;29:562–7.
Gungor G, Tatar D, Salturk C, Cimen P, Karakurt Z, Kirakli C, et al. Why do patients with interstitial lung diseases fail in the ICU? A 2-center cohort study. Respir Care. 2013;58:525–31.
Yokoyama T, Tsushima K, Yamamoto H, Koizumi T, Kubo K. Potential benefits of early continuous positive pressure ventilation in patients with rapidly progressive interstitial pneumonia. Respirol. Carlton Vic. 2012;17:315–21.
Aliberti S, Messinesi G, Gamberini S, Maggiolini S, Visca D, Galavotti V, et al. Non-invasive mechanical ventilation in patients with diffuse interstitial lung diseases. Bmc Pulm. Med. [Internet]. 2014; [cited 2017 Nov 26];14. Available from: https://doi.org/10.1186/1471-2466-14-194.
Fumeaux T, Rothmeier C, Jolliet P. Outcome of mechanical ventilation for acute respiratory failure in patients with pulmonary fibrosis. Intensive Care Med. 2001;27:1868–74.
Stern JB, Mal H, Groussard O, Brugière O, Marceau A, Jebrak G, et al. Prognosis of patients with advanced idiopathic pulmonary fibrosis requiring mechanical ventilation for acute respiratory failure. Chest. 2001;120:213–9.
Molina-Molina M, Badia JR, Marín-Arguedas A, Xaubet A, Santos MJ, Nicolás JM, et al. Outcomes and clinical characteristics of patients with pulmonary fibrosis and respiratory failure admitted to an intensive care unit. A study of 20 cases. Med Clin (Barc). 2003;121:63–7.
Vincent F, Gonzalez F, Do C-H, Clec’h C, Cohen Y. Invasive mechanical ventilation in patients with idiopathic pulmonary fibrosis or idiopathic non-specific interstitial pneumonia. Intern Med Tokyo Jpn. 2011;50:173–4. author reply 175
Gaudry S, Vincent F, Rabbat A, Nunes H, Crestani B, Naccache JM, et al. Invasive mechanical ventilation in patients with fibrosing interstitial pneumonia. J Thorac Cardiovasc Surg. 2014;147:47–53.
Uhlig U, Uhlig S. Ventilation-Induced Lung Injury. In: Terjung R, editor. Compr. Physiol. [Internet]. Hoboken: Wiley; 2011 [cited 2017 Nov 29]. Available from: https://doi.org/10.1002/cphy.c100004.
Nava S, Rubini F. Lung and chest wall mechanics in ventilated patients with end stage idiopathic pulmonary fibrosis. Thorax. 1999;54(5):390.
West JR, Alexander JK. Studies on respiratory mechanics and the work of breathing in pulmonary fibrosis. Am J Med. 1959;27:529–44.
Brodie D, Bacchetta M. Extracorporeal membrane oxygenation for ARDS in adults. N Engl J Med. 2011;365:1905–14.
Marasco SF, Lukas G, McDonald M, McMillan J, Ihle B. Review of ECMO (extra corporeal membrane oxygenation) support in critically ill adult patients. Heart Lung Circ. 2008;17(Suppl 4):S41–7.
Fuehner T, Kuehn C, Hadem J, Wiesner O, Gottlieb J, Tudorache I, et al. Extracorporeal membrane oxygenation in awake patients as bridge to lung transplantation. Am J Respir Crit Care Med. 2012;185:763–8.
Abrams D, Javidfar J, Farrand E, Mongero LB, Agerstrand CL, Ryan P, et al. Early mobilization of patients receiving extracorporeal membrane oxygenation: a retrospective cohort study. Crit. Care Lond. Engl. 2014;18:R38.
Barrett NA, Camporota L. The evolving role and practical application of extracorporeal carbon dioxide removal in critical care. Crit. Care Resusc. J. Australas. Acad Crit Care Med. 2017;19:62–7.
Braune S, Sieweke A, Brettner F, Staudinger T, Joannidis M, Verbrugge S, et al. The feasibility and safety of extracorporeal carbon dioxide removal to avoid intubation in patients with COPD unresponsive to noninvasive ventilation for acute hypercapnic respiratory failure (ECLAIR study): multicentre case-control study. Intensive Care Med. 2016;42:1437–44.
Vianello A, Arcaro G, Paladini L, Iovino S. Successful management of acute respiratory failure in an idiopathic pulmonary fibrosis patient using an extracorporeal carbon dioxide removal system. Sarcoidosis Vasc. Diffuse lung dis. Off. J Wasog. 2016;33:186–90.
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About this article
- Interstitial lung diseases
- Idiopathic pulmonary fibrosis
- Acute respiratory failure
- Invasive ventilation
- Non-invasive ventilation
- High-flow nasal cannula