Diagnostic Yield, Safety and Impact of Transbronchial Lung Biopsy in Mechanically Ventilated Critically Ill Patients: A Retrospective Study

Abstract

Background

Pulmonary infiltrates of variable etiology are one of the main reasons for hypoxemic respiratory failure leading to invasive mechanical ventilation. If pulmonary infiltrates remain unexplained or progress despite treatment, the histopathological result of a lung biopsy could have significant impact on change in therapy. Surgical lung biopsy is the commonly used technique, but due to its considerable morbidity and mortality, less invasive bronchoscopic transbronchial lung biopsy (TBLB) may be a valuable alternative.

Methods

Retrospective, monocentric, observational study in mechanically ventilated, critically ill patients, subjected to TBLB due to unexplained pulmonary infiltrates in the period January 2014 to July 2019. Patients` medical records were reviewed to obtain data on baseline clinical characteristics, modality and adverse events (AE) of the TBLB, and impact of the histopathological results on change in therapy. A multivariable binary logistic regression analysis was performed to identify predictors of AE and hospital mortality, and survival curves were generated using the Kaplan-Meier method.

Results

Forty-two patients with in total 42 TBLB procedures after a median of 12 days of mechanical ventilation were analyzed, of which 16.7% were immunosuppressed, but there was no patient with prior lung transplantation. Diagnostic yield of the TBLB was 88.1%, with AE occurring in 11.9% (most common pneumothorax and minor bleeding). 92.9% of the procedures were performed as a forceps biopsy, with organizing pneumonia (OP) being the most common histological diagnosis (54.8%). Variables independently associated with hospital mortality were age (odds ratio 1.070, 95%CI 1.006–1.138; p = 0.031) and the presence of OP (0.182, [0.036–0.926]; p = 0.040), the latter being confirmed in the survival analysis (log-rank p = 0.040). In contrast, a change in therapy based on histopathology alone occurred in only 40.5%, and there was no evidence of a survival benefit in those patients.

Conclusions

Transbronchial lung biopsy remains a valuable alternative to surgical lung biopsy in mechanically ventilated critically ill patients. However, the high diagnostic yield must be weighed against potential adverse events and limited consequence of the histological result regarding treatment decisions in such patients.

Background

Intubation with mechanical ventilation is a life–saving procedure for patients with acute severe hypoxemic respiratory failure due to pulmonary infiltrates of variable etiology [1]. If infiltrates remain unexplained or progress despite therapy (e.g. antibiotics), it is almost impossible to derive a specific diagnosis based solely on clinical symptoms, radiological findings, and laboratory values. Empiric treatment of such patients tends to over–therapy, that may have potentially toxic side effects (e.g. for unnecessary application of broad-spectrum and long-term antimicrobial agents). This also generates high costs and rare and potentially reversible causes of pulmonary infiltrates remain undetected and untreated. In contrast, the histopathological result of a lung biopsy may provide important information on the underlying disease and could have significant impact on treatment decisions. Surgical lung biopsy (SLB) is the commonly used technique in such patients [2–3], but hypoxemia may worsen dramatically with single–lung ventilation, and the procedure usually requires a transfer from the intensive care unit (ICU) to the operating theater. Alternatively, bronchoscopic, transbronchial lung biopsy (TBLB, by means of forceps biopsy or cryobiopsy) is available, which also can be performed at the bedside in the ICU in the event of mechanical ventilation [4–9].

The present study aims to assess diagnostic yield, safety, and therapeutic consequences of transbronchial lung biopsy in a cohort of mechanically ventilated, critically ill patients.

Methods

Exploratory, retrospective, monocentric, observational study on mechanically ventilated, critically ill patients, treated at the Schillerhoehe Lung Clinic (Gerlingen, Germany) from January 2014 to July 2019, and subjected to transbronchial lung biopsy due to unexplained pulmonary infiltrates. The study was approved by the local ethics committee, the need for informed consent was waived (ethics committee of the State Chamber of Physicians of Baden-Wuerttemberg, Germany, file number F–2019–096).

Results

Forty-two patients with in total 42 TBLB procedures were assessed, of which seven patients (16.7%) were immunosuppressed, but there was no patient with prior lung transplantation. Three patients were on Methotrexate due to rheumatoid arthritis and polymyalgia rheumatica, two patients on Cyclophosphamide pulse therapy due to interstitial lung disease (ILD) associated with hypersensitivity pneumonia and systemic sclerosis, one patient was on neoadjuvant chemotherapy with Cisplatin/Paclitaxel due to non-small cell lung cancer, and one patient received Tacrolimus due to focal segmental glomerulosclerosis. The most common clinical diagnosis leading to mechanical ventilation was pneumonia (52.4%), and 25 patients (59.5%) met the ARDS Berlin criteria [Table 1].

All patients had bilateral infiltrates on chest CT scan at the time of the TBLB. Median time from intubation to TBLB was 12 days (range 4–98 days).A transbronchial forceps biopsy was performed in 92.9% of cases, 83.3% of the biopsies were performed in the ICU, and fluoroscopy was usedin 11.9% of all procedures (and always for cryobiopsy).Right lung biopsy was performed in 57.1% and 50% of all samples were takenfromtwo lung lobes (most often from the rightupper [RUL]and right lower lobe [RLL]).42.9% of all biopsies were performed under chest drainage protection [Table 2].

Table 2: Modality of transbronchial lung biopsy

Legend

Continuous variables are presented as mean values (± standard deviation); categorical variables are presentedas number or number (%).Thrombosis Prophylaxis refers to Enoxaparin (≤ 40 mg/day s.c.) or unfractionated heparin (≤ 15.000 U/day s.c.)

Abbreviations:P/F ratio, ratio of partial pressure of oxygen to fraction of inspired oxygen; FiO₂, fraction of inspired oxygen; IPAP, inspiratory positive airway pressure; PEEP, positive end-expiratory pressure; LTC_dyn, dynamic lung-thorax compliance; INR, International Normalized Ratio; aPTT, activated partial thromboplastin time; ASS, acetylsalicylic acid (100 mg/day)

The median effective number of specimens obtained (and ultimately analyzed by the pathologists)in 40 patients was 4 (range 2–9) and the median size of thesespecimens was 3 mm (range 2–7 mm);this information was missing in two patients (4.8%).Diagnostic yield of the TBLBwas 88.1%, meaning that TBLB revealed a specific histological diagnosis in 37 patients, withOPbeing the most common one (54.8%).Sixteen patients (38.1%) were clinically classified as SOP (9 patients with pneumonia as the leading cause of intubation, 6 postoperative patients, and 1 patient with ANCA-associated vasculitis) and seven patients (16.7%) as COP.A diagnosis of drug-induced lung injury (DILI) was made in four patients,of which three patients experienced Amiodarone-induced pulmonary toxicity, and another four patients showed diffuse alveolar damage (DAD). In fivepatients (11.9%), either there was no lung tissue in the biopsy sample or the histological pattern was not classifiable.No biopsy showed more than one histological diagnosis, and no patient underwent subsequent SLB.Bronchial lavage (BL) was performed in 41 patients (97.6%),and 21 patients (50.0%) were subjected to BAL.There was evidence of infection from BL in 11 patients (26.8%). The mean amount of aspirated liquid in the BAL was 33 mL (± 10 mL);with pure neutrophilia as the most frequent cell distributionin the whole population (57.1%) and in patients with OP (58.3%)[Table 3].

Table 3: Results of transbronchial lung biopsy, bronchiallavage and BAL

Legend

Normal cell distribution of BAL refers to ≥ 85% of alveolar macrophages, ≤ 15% lymphocytes, ≤ 3% neutrophils, and ≤ 1% eosinophils.

 Abbreviations:OP, organizing pneumonia;ILD, interstitial lung disease; PCR, polymerase chain reaction

Eightadverse events were recorded in five patients (11.9%). Pneumothorax,occurring in three patients (7.1%) who all required a chest drainage,was amongst the most commonAE.However, TBLB was performed with chest drainage protection in 18 patients, so that frequencyincreased to 12.5% whenpneumothoraces wererelated to only patients without such a protection.One pneumothorax occurred after cryobiopsy and the othersoccurred as a result of forceps biopsy, but no patient developed a persistent air leak.Biopsies leading to pneumothorax were performed in the RUL/RLL (twice) and in the RLL (once). Minor bleeding occurred in 7.1%, but there was no major bleeding event.One patient died as result of forceps biopsy with tension pneumothoraxand persistent hemodynamic instability with shockdespite immediate chest tube insertion [Table 4].

Table 4:Adverse eventsof transbronchial lung biopsy

Legend

Categorical variables are presentedas number (%).

Abbreviations: AE, adverse event(s)

The histopathological results of the TBLB resulted in a change in therapy in 17 patients (40.5%).Corticosteroids were initiated in 15 patients (12 patients with OP, two patients with DILI, and one patient with DAD);one patient with pre-existing and acute exacerbated ILD was switched from cyclophosphamide pulse therapy to rituximab, and one patient with a histological diagnosis of DAD discontinued corticosteroid treatment.

In patients with corticosteroid induction a median cumulative dose of 600 mg [range 500–4000 mg] of prednisolone was administered within the first week. Responsiveness to corticosteroids with marked improvement in gas exchange (as defined above) could be observed in five patients (which all had histologically confirmed OP;median increase in P/F ratio by day sevenof127 mmHg [105–137 mmHg], compared to 15.5 mmHg [-32–84 mmHg] in ten non-responders [seven OP, one DAD, two DILI]). There was no significant difference in the cumulative prednisolone dose between responders and non-responders (median 500 mg [500–4000 mg] vs 600 mg [500–1180 mg]; p = 0.292).

ICU and hospital mortality in the whole population wereas high as 35.7% and 40.5%, respectively.Patients with a histological diagnosis of OPshowed a trend towards lower ICU mortality (21.7% vs 50.0%; p = 0.079) and lower hospital mortality (26.1% vs 57.1%; p = 0.062).In contrast, there was no difference in ICU mortality (29.4% vs 35.0%; p = 0.721) or hospital mortality (29.4% vs 45.0%; p = 0.337) of patients with and without a change in therapy due to the histopathological result of the TBLB.

In the multivariable binary logistic regression analysis, age (odds ratio 1.070, 95%CI 1.006–1.138; p = 0.031) and the presence of a histological pattern of OP (0.182, [0.036–0.926]; p = 0.040) were independently associated with hospital mortality. This benefit in terms of survival in patients with OP was confirmed by Kaplan-Meier analysis [Figure 1].

There was no independent association of AE with coagulation parameters, the presence of anticoagulants, or with ventilator variables and respiratory indices (e.g. PEEP, IPAP or mechanical power), and no variable could reliably predict a histological diagnosis of OP before TBLB or a response to glucocorticoid treatment.

Discussion

To the best of our knowledge, the present study examined the largest number of critically ill patients (without prior lung transplantation) who underwent a transbronchial lung biopsy due to unexplained pulmonary infiltrates while receiving mechanical ventilation, and the results can be summarized as follows. Diagnostic yield of the TBLB in this group of patients was high (88%). Serious, life-threatening complications were rare events, but they can`t be completely excluded. In contrast, the impact of the histological result on change in therapy of those patients was low and had no perceptible effect on patient`s outcome. For patients with histologically confirmed organizing pneumonia, there was evidence of better survival.

Diagnostic yield of TBLB was high when compared to previous studies. O'Brien and colleagues reported a diagnostic yield of 34.9% in 71 patients with in total 83 TBLB procedures [6]. The proportion of patients with prior lung transplantation or immunosuppression was higher (72%) than in the present study and only 2.5% of all patients showed a specific pathology of OP. In contrast, Bulpa et al. demonstrated a yield of 63%, which increased to a maximum of 74% by combination with BAL [7]. Again, the proportion of histologically confirmed OP was low (10.5%), which may explain the relatively higher diagnostic yield in the present study [15]. Another study on mechanically ventilated, lung transplant recipients revealed predominantly pathologies of acute rejection, often combined with DAD. Diagnostic yield of the TBLB was 56.4% and the gain in histological diagnoses by SLB was up to 33%, which was associated with a change in therapy in 37% [8]. This was predominantly due to a low sensitivity of the TBLB to acute and especially chronic rejection (36% and 0%, respectively). In summary, comparisons of the existing studies in terms of diagnostic yield are difficult to interpret due to different patient characteristics (associated with different histological diagnoses) and lack of comparison of the TBLB with a reference test (e.g. SLB or autopsy) in most cases.

Complication rate of the TBLB was low (11.9%) in the present study, although there was one serious adverse event with ultimately fatal outcome. In contrast, complications after SLB in mechanically ventilated patients occur in about 29%, which are mainly attributable to a high number of persistent air-leaks [2]. Pneumothorax incidence (12.5%) was comparable to previous studies [6–7] although one pneumothorax was related to transbronchial cryobiopsy, and there was no case of persistent air-leak. Incidence of pneumothorax in spontaneously breathing patients varies between 1–6% [16–17], which seems to be slightly lower than in patients receiving mechanical ventilation [6–7] or for transbronchial cryobiopsy [18]. There is evidence for an increased risk of pneumothorax in spontaneously breathing patients after biopsy of the upper lobes. This is most likely a result of the apicobasal pleural pressure gradient in the upright body position (with the most negative pressures in the apex of the thoracic cavity) [17], but there is uncertainty about whether this is also true for mechanically ventilated patients. In addition, the subgroup of ventilated lung transplant recipients probably experience an even lower pneumothorax risk due to pre-existing pleural adhesions [9]. No serious bleeding events occurred, which previously have been reported in up to 5% for transbronchial forceps biopsy [19]. In summary, the more favorable risk profile of the TBLB compared to the SLB must be weighed against its lower diagnostic yield, leading to a higher probability of misclassification of a disease, which can be fatal in the case of respiratory failure with mechanical ventilation, since an incorrect treatment is ineffective or may be even harmful.

Therapeutic consequence of the TBLB was low in the present study, with most frequently corticosteroid treatment started. Response to steroids largely depends on the histological diagnosis and is high in patients with eosinophilic pneumonia or COP, although response in patients with SOP is often unpredictable [20]. Responsiveness was defined analogously to previous studies based on changes in the P/F ratio after 7 days of corticosteroid therapy [12–13]. This may insufficiently reflect the course of the disease, since pulmonary infiltrates often regress over several weeks of therapy and assessment of radiographic changes over time was not part of our analyses.

In-hospital mortality was high in the present study and this is in line with previous results on SLB performed in mechanically ventilated patients, which showed a hospital mortality of up to 60% depending on the histological diagnosis [2]. Patients with a histopathology of OP showed a favorable clinical outcome, which may in part be attributable to the frequently observed change in therapy (e.g. initiation of corticosteroid treatment), but also may be related to an occasionally observed spontaneous improvement of the disease, which has been reported for COP [21]. Gerard and co-workers reported similar results, demonstrating a survival benefit of ARDS patients with a steroid-sensitive pathology on SLB [3]. In contrast, patients with a change in therapy based on the histopathological result showed no advantage in survival in the present study, which may be either related to the small number of cases, but fundamentally raises the question of the benefits of the TBLB in such patients.

Our study has several limitations. First, it was a retrospective, monocentric analysis, and the number of patients assessed was small. Therefore, external validity is uncertain and interpretation of the results should be done with caution. Another major limitation is the lack of comparison of the histological results of the TBLB with those of a reference test, i.e. SLB as the gold standard. Diagnostic accuracy of the TBLB, which reflects the percentage of histologically true positive (test positive and diseases present) and true negative (test negative and disease absent) classified patients, can only be determined with such a comparison. So far, this only exists for mechanically ventilated lung transplant recipients [8], and for patients with interstitial lung disease subjected to transbronchial cryobiopsy [22]. No patient subsequently underwent SLB in the present study, most probably due to the high diagnostic yield of the TBLB, and the low percentage of immunosuppressed patients (limiting differential diagnoses of the pulmonary infiltrates). In this context, the additional diagnostic benefit of the SLB may have appeared to be low, leading to reluctance in performing this procedure considering its significant morbidity and mortality.

Conclusions

Diagnostic yield of a transbronchial lung biopsy in mechanically ventilated, critically ill patients with unexplained pulmonary infiltrates was high and therefore appears to be a suitable alternative to SLB. Complication rate is low, although serious and fatal adverse events can`t be completely excluded, which must be weighed against the limited therapeutic consequence and the apparent lack of benefit in survival in patients with a change in treatment based on the histopathological result.

Abbreviations

95%CI: 95% confidence interval

AE: Adverse event(s)

aPTT: activated partial thromboplastin time

ARDS: Acute respiratory distress syndrome

BAL: Bronchoalveolar lavage

BL: Bronchial lavage

COP: Cryptogenic organizing pneumonia

DAD: Diffuse alveolar damage

DILI: Drug-induced lung injury

ICU: Intensive care unit

FiO₂: Fraction of inspired oxygen

ILD: Interstitial lung disease

INR: International Normalized Ratio

LOS: Length of stay

OP: Organizing pneumonia

P/F ratio: Ratio of partial pressure of oxygen to fraction of inspired oxygen

RLL: Right lower lobe

RUL: Right upper lobe

SLB: Surgical lung biopsy

SOP: Secondary organizing pneumonia

TBLB: Transbronchial lung biopsy

Declarations

Ethics approval and consent to participate

The study was approved by the local ethics committee, the need for informed consent was waived (ethics committee of the State Chamber of Physicians of Baden-Wuerttemberg, Germany, file number F-2019-096).

Consent for publication

Not applicable.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Competing interests

AG and CN have disclosed that they do not have any conflicts of interest.

Funding

None.

Authors` contributions

All authors had full access to all of the data in the study. AG serves as guarantor of the paper, takes responsibility for data acquisition, the integrity of the data, the accuracy of the data analysis, and performed the statistical analysis. CN contributed to data analysisand revision of the manuscript. All authors have read and approved the final version of the manuscript.

Acknowledgements

Not applicable.

References

1. Esteban A, Frutos-Vivar F, Muriel A, et al. Evolution of mortality over time in patients receiving mechanical ventilation. Am J Respir Crit Care Med. 2013;188:220–30.
2. Wong AK, Walkey AJ. Open lung biopsy among critically ill, mechanically ventilated patients: A Metaanalysis. Ann Am Thorac Soc. 2015;12:1226–30.
3. Gerard L, Bidoul T, Castanares-Zapatero D, et al. Open lung biopsy in nonresolving acute respiratory distress syndrome commonly identifies corticosteroid-sensitive pathologies, associated with better outcome. Crit Care Med. 2018;46:907–14.
4. Papin TA, Grum CM, Weg JG. Transbronchial lung biopsy during mechanical ventilation. Chest. 1986;89:168–70.
5. Pincus PS, Kallenbach JM, Hurwitz MD, et al. Transbronchial lung biopsy during mechanical ventilation. Crit Care Med. 1987;15:1136–9.
6. O`Brien JD, Ettinger NA, Shevlin D, et al. Safety and yield of transbronchial biopsy in mechanically ventilated patients. Crit Care Med. 1997;25:440–6.
7. Bulpa PA, Dive AM, Mertens L, et al. Combined bronchoalveolar lavage and transbronchial lung biopsy: safety and yield in ventilated patients. Eur Respir J. 2003;21:489–94.
8. Burns KE, Johnson BA, Iacono AT. Diagnostic properties of transbronchial biopsy in lung transplant recipients who require mechanical ventilation. J Heart Lung Transplant. 2003;22:267–75.
9. Mohanka MR, Mehta AC, Budey MM, et al. Impact of bedside bronchoscopy in critically ill lung transplant recipients. J Bronchology Interv Pulmonol. 2014;21:199–207.
10. Ranieri VM, Rubenfeld GD, Thompson BT, et al. Acute respiratory distress syndrome: the Berlin definition. JAMA. 2012;307:2526–33.
11. Gagnon S, Quigley N, Dutau H, et al. Approach to hemoptysis in the modern era. Can Respir J. 2017;2017:1565030.
12. Meduri GU, Headley AS, Golden E, et al. Effect of prolonged methylprednisolone therapy in unresolving acute respiratory distress syndrome: a randomized controlled trial. JAMA. 1998;280:159–65.
13. Meduri GU, Golden E, Freire AX, et al. Methylprednisolone infusion in early severe ARDS: results of a randomized controlled trial. Chest. 2007;131:954–63.
14. Herth FJF, Becker HD, Ernst A. Aspirin does not increase bleeding complications after transbronchial lung biopsy. Chest. 2002;122:1461–4.
15. Poletti V, Cazzato S, Minicuci N, et al. The diagnostic value of bronchoalveolar lavage and transbronchial lung biopsy in cryptogenic organizing pneumonia. Eur Respir J. 1996;9:2513–6.
16. Tukey MH, Soylemez Wiener R. Population-based estimates of transbronchial lung biopsy utilization and complications. Respir Med. 2012;106:1559–65.
17. Herout V, Heroutova M, Zdenek M, et al. Transbronchial biopsy from the upper pulmonary lobes is associated with increased risk of pneumothorax – a retrospective study. BMC Pulm Med. 2019;19:56.
18. She S, Steinfort DP, Ing AJ, et al. Transbronchial cryobiopsy in interstitial lung disease: safety of a standardized procedure. J Bronchol Intervent Pulmonol. 2020;27:36–41.
19. Hetzel J, Eberhardt R, Petermann C, et al. Bleeding risk of transbronchial cryobiopsy compared to transbronchial forceps biopsy in interstitial lung disease – a prospective, randomized, multicenter cross-over trial. Respir Res. 2019;20:140.
20. Cordier JF. Cryptogenic organizing pneumonia. Eur Respir J. 2006;28:422–46.
21. Epler GR, Colby TV, McLoud TC, et al. Bronchiolitis obliterans organizing pneumonia. N Engl J Med. 1985;312:152–8.
22. Troy LK, Grainge C, Corte TJ, et al. Diagnostic accuracy of transbronchial lung cryobiopsy for interstitial lung disease diagnosis (COLDICE): a prospective, comparative study. Lancet Respir Med. 2019;8:171–81.