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Abstract

Patients with pulmonary alveolar proteinosis have a restrictive disease and are hypoxic. Lavage of one lung with large quantities of saline requires careful lung isolation. For more than 10 years, bilateral lung lavage has been performed during the same anesthetic period. GM-CSF-associated therapy is now a complementary treatment to WLL for pulmonary alveolar proteinosis, when needed.

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References

  1. Vincente G. Le lavage des poumons. Presse Med. 28:1266–8.

    Google Scholar 

  2. Ramirez-Riviera J. The strange beginnings of diagnostic and therapeutic bronchoalveolar lavage. PRHS. 1992;11(1):27.

    Google Scholar 

  3. Ramirez-Riviera J, Kieffer RF, Ball WC Jr. Bronchopulmonary lavage in man. Ann Intern Med. 1965;63(5):819–28.

    Article  Google Scholar 

  4. Ramirez J. Bronchopulmonary lavage. New techniques and observations. Dis Chest. 1966;50(6):581–8.

    Article  CAS  Google Scholar 

  5. Ramirez-Riviera J, Schultz RB, Dutton RE. Pulmonary alveolar proteinosis: a new technique and rationale for treatment. Arch Intern Med. 1963;112:419–31.

    Article  Google Scholar 

  6. Spragg RG, Benumof JL, Alfery DD. New methods for the performance of unilateral lung lavage. Anesthesiology. 1982;57(6):535–8.

    Article  CAS  Google Scholar 

  7. Bussieres JS. Whole lung lavage. Anesthesiol Clin North Am. 2001;19(3):543–58.

    Article  CAS  Google Scholar 

  8. Wilt JL, Banks DE, Weissman DN, Parker JE, Vallyathan V, Castranova V, et al. Reduction of lung dust burden in pneumoconiosis by whole-lung lavage. J Occup Environ Med. 1996;38(6):619–24.

    Article  CAS  Google Scholar 

  9. Venkateshiah SB, Yan TD, Bonfield TL, Thomassen MJ, Meziane M, Czich C, et al. An open-label trial of granulocyte macrophage colony stimulating factor therapy for moderate symptomatic pulmonary alveolar proteinosis. Chest. 2006;130(1):227–37.

    Article  CAS  Google Scholar 

  10. Trapnell BC, Whitsett JA, Nakata K. Pulmonary alveolar proteinosis. N Engl J Med. 2003;349(26):2527–39.

    Article  CAS  Google Scholar 

  11. Huizar I, Kavuru MS. Alveolar proteinosis syndrome: pathogenesis, diagnosis, and management. Curr Opin Pulm Med. 2009;15(5):491–8.

    Article  Google Scholar 

  12. Lee K, Levin D, Webb W, Chen D, Storto M, Golden J. Pulmonary alveolar proteinosis: high-resolution CT, chest radiographic, and functional correlations. Chest. 1997;111:989–95.

    Article  CAS  Google Scholar 

  13. Arcasoy SM, Lanken PN. Images in clinical medicine. Pulmonary alveolar proteinosis. N Engl J Med. 2002;347(26):2133.

    Article  Google Scholar 

  14. Wong CA, Wilsher ML. Treatment of exogenous lipoid pneumonia by whole lung lavage. Aust NZ J Med. 1994;24(6):734–5.

    Article  CAS  Google Scholar 

  15. Martin RJ, Rogers RM, Myers NM. PUlmonary alveolar proteinosis: shunt fraction and lactic acid dehydrogenase concentration as aids to diagnosis. Am Rev Respir Dis. 1978;117(6):1059–62.

    CAS  PubMed  Google Scholar 

  16. Costello JF, Moriarty DC, Branthwaite MA, Turner-Warwick M, Corrin B. Diagnosis and management of alveolar proteinosis: the role of electron microscopy. Thorax. 1975;30(2):121–32.

    Article  CAS  Google Scholar 

  17. Gilmore LB, Talley FA, Hook GE. Classification and morphometric quantitation of insoluble materials from the lungs of patients with alveolar proteinosis. Am J Pathol. 1988;133(2):252–64.

    CAS  PubMed  PubMed Central  Google Scholar 

  18. Seymour JF, Presneill JJ. Pulmonary alveolar proteinosis: progress in the first 44 years. Am J Respir Crit Care Med. 2002;166(2):215–35.

    Article  Google Scholar 

  19. Goldstein LS, Kavuru MS, Curtis-McCarthy P, Christie HA, Farver C, Stoller JK. Pulmonary alveolar proteinosis: clinical features and outcomes. Chest. 1998;114(5):1357–62.

    Article  CAS  Google Scholar 

  20. Rubinstein I, Mullen JB, Hoffstein V. Morphologic diagnosis of idiopathic pulmonary alveolar lipoproteinosis-revisited. Arch Intern Med. 1988;148(4):813–6.

    Article  CAS  Google Scholar 

  21. Bonfield TL, Kavuru MS, Thomassen MJ. Anti-GM-CSF titer predicts response to GM-CSF therapy in pulmonary alveolar proteinosis. Clin Immunol. 2002;105(3):342–50.

    Article  CAS  Google Scholar 

  22. Lin FC, Chang GD, Chern MS, Chen YC, Chang SC. Clinical significance of anti-GM-CSF antibodies in idiopathic pulmonary alveolar proteinosis. Thorax. 2006;61(6):528–34.

    Article  Google Scholar 

  23. Kavuru MS, Popovich M. Therapeutic whole lung lavage: a stop-gap therapy for alveolar proteinosis. Chest. 2002;122(4):1123–4.

    Article  Google Scholar 

  24. Borie R, Debray MP, Laine C, Aubier M, Crestani B. Rituximab therapy in autoimmune pulmonary alveolar proteinosis. Eur Respir J. 2009;33(6):1503–6.

    Article  CAS  Google Scholar 

  25. Luisetti M, Rodi G, Perotti C, Campo I, Mariani F, Pozzi E, et al. Plasmapheresis for treatment of pulmonary alveolar proteinosis. Eur Respir J. 2009;33(5):1220–2.

    Article  CAS  Google Scholar 

  26. Garber B, Albores J, Wang T, Neville TH. A plasmapheresis protocol for refractory pulmonary alveolar proteinosis. Lung. 2015;193(2):209–11.

    Article  CAS  Google Scholar 

  27. Parker LA, Novotny D. Recurrent alveolar proteinosis following double lung transplantation. Chest. 1997;111:1457.

    Article  CAS  Google Scholar 

  28. Loubser PG. Validity of pulmonary artery catheter-derived hemodynamic information during bronchopulmonary lavage. J Cardiothorac Vasc Anesth. 1997;11(7):885–8.

    Article  CAS  Google Scholar 

  29. Cohen E, Eisenkraft JB. Bronchopulmonary lavage: effects on oxygenation and hemodynamics. J Cardiothorac Anesth. 1990;4(5):609–15.

    Article  CAS  Google Scholar 

  30. McMahon CC, Irvine T, Conacher ID. Transoesophageal echocardiography in the management of whole lung lavage. Br J Anaesth. 1998;81(2):262–4.

    Article  CAS  Google Scholar 

  31. Swenson JD, Astle KL, Bailey PL. Reduction in left ventricular filling during bronchopulmonary lavage demonstrated by transesophageal echocardiography. Anesth Analg. 1995;81(3):634–7.

    CAS  PubMed  Google Scholar 

  32. Bardoczky GI, Engelman E, d'Hollander A. Continuous spirometry: an aid to monitoring ventilation during operation. Br J Anaesth. 1993;71(5):747–51.

    Article  CAS  Google Scholar 

  33. Hammon WE, McCaffree DR, Cucchiara AJ. A comparison of manual to mechanical chest percussion for clearance of alveolar material in patients with pulmonary alveolar proteinosis (phospholipidosis). Chest. 1993;103(5):1409–12.

    Article  CAS  Google Scholar 

  34. Bracci L. Role of physical therapy in management of pulmonary alveolar proteinosis. A case report. Phys Ther. 1988;68(5):686–9.

    Article  CAS  Google Scholar 

  35. Bingisser R, Kaplan V, Zollinger A, Russi EW. Whole-lung lavage in alveolar proteinosis by a modified lavage technique. Chest. 1998;113(6):1718–9.

    Article  CAS  Google Scholar 

  36. Nadeau MJ, Cote D, Bussieres JS. The combination of inhaled nitric oxide and pulmonary artery balloon inflation improves oxygenation during whole-lung lavage. Anesth Analg. 2004;99(3):676–9. table of contents.

    Article  Google Scholar 

  37. Julien T, Caudine M, Barlet H, Wintrebert P, Aubas P, du Cailar J. Effect of positive end expiratory pressure on arterial oxygenation during bronchoalveolar lavage for proteinosis. Annales francaises d’anesthesie et de reanimation. 1986;5(2):173–6.

    Article  CAS  Google Scholar 

  38. Moutafis M, Dalibon N, Colchen A, Fischler M. Improving oxygenation during bronchopulmonary lavage using nitric oxide inhalation and almitrine infusion. Anesth Analg. 1999;89(2):302–4.

    CAS  PubMed  Google Scholar 

  39. Biervliet J, Peper J, Roos C, et al. Whole-lung lavage under hyperbaric conditions. In: Erdmann W, editor. Oxygen transport to tissue XIV. NewYork: Plenum Press; 1992.

    Google Scholar 

  40. Vymazal T, Krecmerova M. Respiratory strategies and airway management in patients with pulmonary alveolar proteinosis: a review. Biomed Res Int. 2015;2015:639543.

    Article  Google Scholar 

  41. Cohen ES, Elpern E, Silver MR. Pulmonary alveolar proteinosis causing severe hypoxemic respiratory failure treated with sequential whole-lung lavage utilizing venovenous extracorporeal membrane oxygenation: a case report and review. Chest. 2001;120(3):1024–6.

    Article  CAS  Google Scholar 

  42. Chauhan S, Sharma KP, Bisoi AK, Pangeni R, Madan K, Chauhan YS. Management of pulmonary alveolar proteinosis with whole lung lavage using extracorporeal membrane oxygenation support in a postrenal transplant patient with graft failure. Ann Card Anaesth. 2016;19(2):379–82.

    Article  Google Scholar 

  43. Hasan N, Bagga S, Monteagudo J, Hirose H, Cavarocchi NC, Hehn BT, et al. Extracorporeal membrane oxygenation to support whole-lung lavage in pulmonary alveolar proteinosis: salvage of the drowned lungs. J Bronchology Interv Pulmonol. 2013;20(1):41–4.

    Article  Google Scholar 

  44. Zhou B, Zhou HY, Xu PH, Wang HM, Lin XM, Wang XD. Hyperoxygenated solution for improved oxygen supply in patients undergoing lung lavage for pulmonary alveolar proteinosis. Chin Med J. 2009;122(15):1780–3.

    CAS  PubMed  Google Scholar 

  45. Ciravegna B, Sacco O, Moroni C, Silvestri M, Pallecchi A, Loy A, et al. Mineral oil lipoid pneumonia in a child with anoxic encephalopathy: treatment by whole lung lavage. Pediatr Pulmonol. 1997;23(3):233–7.

    Article  CAS  Google Scholar 

  46. McKenzie B, Wood RE, Bailey A. Airway management for unilateral lung lavage in children. Anesthesiology. 1989;70(3):550–3.

    Article  CAS  Google Scholar 

  47. Paquet C, Karsli C. Technique of lung isolation for whole lung lavage in a child with pulmonary alveolar proteinosis. Anesthesiology. 2009;110(1):190–2.

    Article  Google Scholar 

  48. Moazam F, Schmidt JH, Chesrown SE, Graves SA, Sauder RA, Drummond J, et al. Total lung lavage for pulmonary alveolar proteinosis in an infant without the use of cardiopulmonary bypass. J Pediatr Surg. 1985;20(4):398–401.

    Article  CAS  Google Scholar 

  49. Hiratzka LF, Swan DM, Rose EF, Ahrens RC. Bilateral simultaneous lung lavage utilizing membrane oxygenator for pulmonary alveolar proteinosis in an 8-month-old infant. Ann Thorac Surg. 1983;35(3):313–7.

    Article  CAS  Google Scholar 

  50. Lippmann M, Mok MS, Wasserman K. Anaesthetic management for children with alveolar proteinosis using extracorporeal circulation. Report of two cases. Br J Anaesth. 1977;49(2):173–7.

    Article  CAS  Google Scholar 

  51. Tsai WC, Lewis D, Nasr SZ, Hirschl RB. Liquid ventilation in an infant with pulmonary alveolar proteinosis. Pediatr Pulmonol. 1998;26(4):283–6.

    Article  CAS  Google Scholar 

  52. Libbey J. Anesthésie-Réanimation en Chirurgie Thoracique. In: Bussières JS, Léone M. Anesthésie-Réanimation en Chirurgie Thoracique. Paris: Arnette-Collection verte, John Libbey; 2017

    Google Scholar 

  53. Slinger PD. Principles and practice of anesthesia for thoracic surgery. 1st ed. New York/London: Springer; 2011.

    Book  Google Scholar 

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Clinical Case Discussion

Clinical Case Discussion

A 47-year-old woman was referred to our team for WLL 10 years ago (2008). At that time, she presented some symptoms, mainly increasing dyspnea, for 6 months. An open lung biopsy had been performed at her hospital to establish the diagnosis of PAP. Pulmonary function tests performed in our center showed a light restrictive syndrome, a DLCO at 58%, and a PaO2 of 68 mmHg. Radiological investigation revealed a homogeneous distribution with the involvement of bilateral superior lobes, middle lobe, and bilateral supero-dorsal segment of the inferior lobe. BAL confirmed the diagnosis of PAP.

A first bilateral WLL was performed, and moderately effective results were obtained. During the next 2.5-year period, the patient underwent six bilateral WLL, at intervals varying between 4 and 12 months, without good improvement in the clinical status, laboratory results, and radiological imaging. During the last WLL, BAL was performed as the radiological infiltrations were localized mainly in the left superior lobe and the supero-dorsal segment of the bilateral inferior lobes.

Nine months later, the patient complained about the same symptoms without marked improvement following any of the performed WLL. The dosage of GM-CSF was measured, and the dosage result, 203 μg/mL (N < 3 μg/ml), confirmed the diagnosis of primary PAP. In the following months, the patient received GM-CSF, but this treatment was ended because no improvement occurred and many secondary effects were observed. A few months later, the patient was placed on rituximab (Rituxan®), but the treatment was also ended after a few cycles since there was clinical and radiological deterioration.

Given this situation, we performed a new WLL, associated with specific BAL. The sediment recuperation was increased following the BAL. In the following days after the recovery from the WLL, we began GM-CSF by inhalation, once daily. At 1- and 3-month follow-up, the patient presented a significant improvement of her clinical status, for the first time since the first WLL. The radiologic images were completely cleared with this associated therapy, but the laboratory investigation remained stable.

We followed her to evaluate the long-term effect of this therapy. Up to 4 years after the last WLL, she received GM-CSF by inhalation following the yearly CT scan imaging, since the images reported small infiltrations. The last follow-up was done 8 years following the last WLL, and she was still asymptomatic. The annual CT scan was clean, as for the last four ones, and she did not take any GM-CSF inhalation.

This case report promotes the usefulness of a multimodal therapy that should be carried out to efficiently treat patients suffering from PAP.

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Bussières, J.S., Couture, E.J. (2019). Whole Lung Lavage. In: Slinger, P. (eds) Principles and Practice of Anesthesia for Thoracic Surgery. Springer, Cham. https://doi.org/10.1007/978-3-030-00859-8_45

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  • DOI: https://doi.org/10.1007/978-3-030-00859-8_45

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