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DOI: 10.1055/s-0043-1769225
Non-bronchoscopic bronchoalveolar lavage (mini-BAL) in critically ill pediatric patients with severe respiratory failure (pARDS) after Hematopoietic stem-cell transplantation (HSCT) – A single-center experience
Introduction The technique of non-bronchoscopic bronchoalveolar lavage (mini-BAL) in pediatrics has been utilized in several studies and involves instillation and re-aspiration of saline (1 mL/kg up to 20 mL) using an in-line suction catheter at the level of the carina [1] [2] [3] [4] [5] [6].
A study in children showed a higher specifity of mini-BAL in pediatric patients compared to endotracheal aspiration (ETA) [2] and is considered to be a generally well-tolerated procedure, although particularly in patients with oxygenation indices (OI) of greater than 20, careful monitoring seems to be requiered.[5]
In adults, BAL is considered important for detection of respiratory tract pathogens in patients with hematological malignancies, particularly invasive pulmonary aspergillosis (IPA) and Pneumocystis jirovecii pneumonia (PJP).[7] Among immunosuppressed children, mini-BAL was successfully utilized in children with HIV-associated chronic lung disease.[6]
A strong correlation between the isolation rates of bacteria and fungi in traditional BAL and mini-BAL samples obtained from immunocompromised adult patients with pneumonia and respiratory failure was documented.[8]
To our knowledge, there are no publications in the literature concerning mini-BAL after Hematopoietic stem-cell transplantation (HSCT).
Aim The aim of this study is to describe the feasibility and clinical relevance of mini-BAL in critically ill pediatric patients with respiratory failure (pARDS) after HSCT in our institution.
Methods A retrospective analysis including 12 intubated pediatric patients undergoing 17 mini-BALs in the setting of pARDS after HCST in our tertiary university hospital in the years 2017 – 2023 was performed.
Results Chart reviews with calculations of OI as well as the vasoactive-inotropic score (VIS) showed no patient-centered complications such as prolonged desaturation, cardiac arrest or significantly increased need for cardiovascular support.
The intervention was performed on average 55 days (5 – 270 days) after HSCT. Mean patient characteristics were an age of 5,9 years (0,3 – 18,3 years) and weight of 22,1 kg (4,9 – 66 kg). The patients had severe pARDS (OI ≥ 16).[9] The mean OI before the mini-BAL was 22,2 (SD +/−12,5), the mean OI after the procedure was 19,9 (SD +/−13,4). The VIS before mini-BAL was 7,7 (SD +/−15) and after the procedure 9 (SD +/−15,3). In 6/17 mini-BAL studies (35,2 %) infectious agents were detected (e.g. C. krusei, Asp. fumigatus, PCJ, CMV).
Conclusion We were able to demonstrate for the first time the feasibility and safety of non-bronchoscopic bronchoalveolar lavage (mini-BAL) in pediatric patients with severe respiratory failure (pARDS) after Hematopoietic stem-cell transplantation (HSCT), even if the oxygenation index is greater than 20. Regarding the relatively high rate of positive findings, the use of mini-BAL sampling in such patients could therefore be a less-invasive, less-costly and simpler alternative to traditional BAL.
Interessenkonflikt
The authors declare no possible conflicts of interest due to economic or personal ties.
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Literatur
- 1 Clark J.A.. et al. The rapid detection of respiratory pathogens in critically ill children. Crit. Care 2023; 27: 11
- 2 Yıldız-Atıkan B., Karapınar B., Aydemir Ş., Vardar F.. Comparison of endotracheal aspirate and non-bronchoscopic bronchoalveolar lavage in the diagnosis of ventilator-associated pneumonia in a pediatric intensive care unit. Turk. J. Pediatr. 2015; 57: 578-586
- 3 Badiee P., Rezapour A., Abbasian A., Foroutan H.R., Jafarian H.. Prevalence of colonization and mitochondrial large subunit rRNA mutation of Pneumocystis jiroveci among Iranian children. Iran. J. Microbiol. 2016; 8: 326-330
- 4 Heaney L.G.. et al. Investigating paediatric airways by non-bronchoscopic lavage: normal cellular data. Clin. Exp. Allergy J. Br. Soc. Allergy Clin. Immunol 1996; 26: 799-806
- 5 Burmester M., Mok Q.. How safe is non-bronchoscopic bronchoalveolar lavage in critically ill mechanically ventilated children?. Intensive Care Med 2001; 27: 716-721
- 6 Singh R., Thula S.A., Jeena P.M.. Lung infiltrates in antiretroviral-naive HIV-infected children with chronic lung disease: value of non-bronchoscopic bronchoalveolar lavage in the detection of Candida albicans. J. Trop. Pediatr 2013; 59: 59-63
- 7 Svensson T., Lundström K.L., Höglund M., Cherif H.. Utility of bronchoalveolar lavage in diagnosing respiratory tract infections in patients with hematological malignancies: are invasive diagnostics still needed?. Ups. J. Med. Sci. 2017; 122: 56-60
- 8 Tasbakan M.S.. et al. Comparison of bronchoalveolar lavage and mini-bronchoalveolar lavage in the diagnosis of pneumonia in immunocompromised patients. Respir. Int. Rev. Thorac. Dis. 2011; 81: 229-235
- 9 Pediatric Acute Lung Injury Consensus Conference Group. Pediatric acute respiratory distress syndrome: consensus recommendations from the Pediatric Acute Lung Injury Consensus Conference. Pediatr Crit Care Med 2015; 16 (05) 428-39
Publikationsverlauf
Artikel online veröffentlicht:
06. Juni 2023
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Rüdigerstraße 14, 70469 Stuttgart, Germany
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Literatur
- 1 Clark J.A.. et al. The rapid detection of respiratory pathogens in critically ill children. Crit. Care 2023; 27: 11
- 2 Yıldız-Atıkan B., Karapınar B., Aydemir Ş., Vardar F.. Comparison of endotracheal aspirate and non-bronchoscopic bronchoalveolar lavage in the diagnosis of ventilator-associated pneumonia in a pediatric intensive care unit. Turk. J. Pediatr. 2015; 57: 578-586
- 3 Badiee P., Rezapour A., Abbasian A., Foroutan H.R., Jafarian H.. Prevalence of colonization and mitochondrial large subunit rRNA mutation of Pneumocystis jiroveci among Iranian children. Iran. J. Microbiol. 2016; 8: 326-330
- 4 Heaney L.G.. et al. Investigating paediatric airways by non-bronchoscopic lavage: normal cellular data. Clin. Exp. Allergy J. Br. Soc. Allergy Clin. Immunol 1996; 26: 799-806
- 5 Burmester M., Mok Q.. How safe is non-bronchoscopic bronchoalveolar lavage in critically ill mechanically ventilated children?. Intensive Care Med 2001; 27: 716-721
- 6 Singh R., Thula S.A., Jeena P.M.. Lung infiltrates in antiretroviral-naive HIV-infected children with chronic lung disease: value of non-bronchoscopic bronchoalveolar lavage in the detection of Candida albicans. J. Trop. Pediatr 2013; 59: 59-63
- 7 Svensson T., Lundström K.L., Höglund M., Cherif H.. Utility of bronchoalveolar lavage in diagnosing respiratory tract infections in patients with hematological malignancies: are invasive diagnostics still needed?. Ups. J. Med. Sci. 2017; 122: 56-60
- 8 Tasbakan M.S.. et al. Comparison of bronchoalveolar lavage and mini-bronchoalveolar lavage in the diagnosis of pneumonia in immunocompromised patients. Respir. Int. Rev. Thorac. Dis. 2011; 81: 229-235
- 9 Pediatric Acute Lung Injury Consensus Conference Group. Pediatric acute respiratory distress syndrome: consensus recommendations from the Pediatric Acute Lung Injury Consensus Conference. Pediatr Crit Care Med 2015; 16 (05) 428-39