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CASE REPORT
Year : 2009  |  Volume : 53  |  Issue : 3  |  Page : 362-366 Table of Contents     

Pulmonary Alveolar Proteinosis with Respiratory Failure-Anaesthetic Management of Whole Lung Lavage


1 Senior consultant, Chest physician, P.D. Hinduja National hospital & Medical research centre, Veer savarkar marg , Mahim, MUMBAI-400016, India
2 Associate Consultant, Chest physician, P.D. Hinduja National hospital & Medical research centre, Veer savarkar marg , Mahim, MUMBAI-400016, India
3 Senior consultant & HOD, Chest physician, P.D. Hinduja National hospital & Medical research centre, Veer savarkar marg , Mahim, MUMBAI-400016, India
4 Consultant, Chest physician, P.D. Hinduja National hospital & Medical research centre, Veer savarkar marg , Mahim, MUMBAI-400016, India

Date of Web Publication3-Mar-2010

Correspondence Address:
Madhavi Desai
Department of Anaesthesiology, P.D.Hinduja National hospital & Medical Research Centre, Veer Savarkar Marg,Mahim,Mumbai400016
India
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Source of Support: None, Conflict of Interest: None


PMID: 20640150

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Pulmonary alveolar proteinosis (PAP) is a rare disorder characterized by accumulation of amorphous acellular phospholipid material in the lungs. Whole lung lavage is the standard therapy which gives dramatic clinical improve­ment and offers a long term survival to these patients.
A 43-year-old man suffering from PAP presented to casualty with NYHA grade IV dyspnoea with oxygen saturation (SaO 2 ) on pulseoximetry 67% on room air and 78% with O 2 6 L/min. He underwent whole lung lavage under general anaesthesia using one lung ventilation with 37 F left end bronchial double lumen tube. The lung lavage was initially performed for the left lung and for the right lung 4 days later. The patient was discharged home with oxygen saturation of 96 % on room air.

Keywords: Pulmonary alveolar proteinosis, Whole lung lavage, Broncho-pulmonary lavage,Anaesthesia


How to cite this article:
Nandkumar S, Desai M, Butani M, Udwadia Z. Pulmonary Alveolar Proteinosis with Respiratory Failure-Anaesthetic Management of Whole Lung Lavage. Indian J Anaesth 2009;53:362-6

How to cite this URL:
Nandkumar S, Desai M, Butani M, Udwadia Z. Pulmonary Alveolar Proteinosis with Respiratory Failure-Anaesthetic Management of Whole Lung Lavage. Indian J Anaesth [serial online] 2009 [cited 2021 Aug 4];53:362-6. Available from: https://www.ijaweb.org/text.asp?2009/53/3/362/60306


   Introduction Top


Pulmonary alveolar proteinosis (PAP), first de­scribed in 1958 by Rosen et al [1], has proved to be a rare but interesting disorder resulting in accumulation of amorphous lipoproteinaceous acellular material in lungs following impaired clearance of surfactant by macrophages. Transgenic murine models have clearly established that hematopoietic growth factor (granulo­cyte-macrophage colony stimulating factor [GM-CSF]) is critical for local regulation of surfactant homeostasis. Additional human studies have linked the presence of a circulating, neutralizing anti-GM-CSF antibody in adults with idiopathic PAP. Therefore, in the current paradigm, there are three major clinical subtypes of PAP: the most common adult idiopathic variety, which is pre­sumably autoimmune (with a circulating anti-GM-CSF antibody); a neonatal variety that is likely due to a de­fect in surfactant proteins B or C or the common B­chain of the GM-CSF receptor; and secondary PAP associated with occupational exposures or immunologic disorders. Preliminary reports from several groups in­dicate that a subset of adult patients with idiopathic PAP respond favorably to GM-CSF therapy. [1] Epidemio­logical data is scarce but one estimate suggests an annual incidence of the order of 2 to 5 per million. The long term outlook for the patients with PAP has greatly improved with use of whole lung lavage.

We report a case of PAP in a patient who was diagnosed 10 years ago. He had undergone whole lung lavage and then was asymptomatic for 10 years .He again presented in acute respiratory failure despite GM-CSF therapy and hence was subjected to whole lung lavage (WLL) which resulted in dramatic clinical and radiological improvement.


   Case report Top


A 43-year-old farmer, who was a known case of PAP presented to casualty with NYHA grade IV dys­pnoea with respiratory rate 28/min, pulse 88/min, BP 100/68 mmHg, oxygen saturation (SaO 2 ) on pulseoximetry 67% on room air and 78% with O 2 6 L/min. The trachea was intubated in casualty, ventilated with FiO 2 1, PEEP 5 cm H 2 O and a respiratory rate of 20 which resulted in peak airway pressure of 40cm H 2 O and SaO 2 of 83% in intensive care unit (ICU). Radiography of chest revealed diffuse bilateral asym­metrical infiltrates which had worsened as compared to his previous X- rays. CT scan of the thorax showed bilateral patchy alveolar filling shadows with air bron­chogram . The trachea was extubated after 48 hours of ventilation and the patient was put on FiO 2 0.6 un­der venturi mask with SaO 2 of 88-89%. He was sched­uled for whole lung lavage.

Patient's blood investigations showed a Hb18.7 g%, haematocrit 53.3%, WBC count 75,000/cmm neutrophils 97%. 2D-Echocardigram showed left ven­tricular ejection fraction (LVEF) 60%, pulmonary ar­tery pressure by jet 20-25 mmHg. The arterial blood gas(ABG) analysis was as follows: PH =7.467, PaO 2 52.1 withFiO 2 0.6, PaCO 2 = 32.2, HCO 3 =23. His blood pressure was 94/56mmHg and heart rate 50/ min.


   Management Top


The whole lung lavage was carried out in the ICU in two sessions. The right internal jugular vein and right radial artery were cannulated under local anaesthesia prior to procedure. The CVP was 10-12 mmHg. After preoxygenataion for 5 minutes the patient was induced with intravenous midazolam 0.05mgKg -1 + fentanyl 6mcgKg -1 , 5 % sevoflurane via inhalation and iv succi­nylcholine 2 mgKg -1 . The trachea was intubated with Broncho-cath 37 F ( Mallinckrodt) left endobronchial double lumen tube (DLT) and ventilated with FiO 2 1 using Aestiva 5(Datex -Ohmeda) ventilator of the ana­esthesia machine. Position of the DLT was confirmed with auscultation and using 2.8 mm ( outer diameter) fiber-optic bronchoscope. Anaesthesia was maintained with midazolam 0.01 mgKg -1 hr -1 + fentanyl 1mcg.kg­-1 .hr -1 , + atracurium 0.4 mg.kg -1 . hr -1 infusion and isoflurane 0.2-1.5%. Dopamine 5mcg.kg -1 min -1 was started along with the induction in view of his pre-pro­cedure haemodynamic status.

ABG analysis was done immediately after induc­tion while both lungs were ventilated with FiO 2 1 when PaO 2 was 65.1mmHg. Since we decided to lavage the left lung first, it was clamped and degassed, while the right lung was ventilated with FiO 2 1 + PEEP 5 cm H 2 O for next 20 minutes. At the end of 20minutes ABG was repeated which showed a PaO 2 of 52.5 mmHg [Table 1]. Since patient tolerated the 20 minutes test of one lung ventilation haemodynamically and maintained PaO 2 fairly, Broncho-pulmonary lavage(BPL) on left lung was performed.

Lavage was performed using 1000 ml - 1200 ml aliquots of normal saline warmed to body temperature; that was rapidly instilled into the left lung. Chest per­cussions were performed for several minutes while the fluid was indwelling to help loosen the proteinacious material. The saline was then withdrawn from the de­gassed lung. The saline was infused and drained by gravity using wide bore tubing with a Y - shape con­nection. Lavages were continued until the effluent sa­line became clear and nonviscous [Figure 1]. This re­quired 10 cycles of lavage with 10.5 L saline. Through­out the procedure invasive blood pressure, CVP, urine output, SaO2, capnography, rectal temperature, re­peated ABG and serum electrolytes were monitored meticulously. Lowest SaO 2 in the lavage was 80%, maximum PaCO 2 60 mm Hg and blood pressure was maintained 95/60- 120/70 mm Hg with dopamine of 5mcg.kg -1 min -1 . After re-expansion of lavaged lung with 100% O 2 the DLT was replaced with standard 8.5 Portex cuffed single lumen endotracheal tube at the end of the procedure. The procedure took 4&½ hours with total affluent saline of 10.5 L, effluent fluid 9.0 and urine output 750 ml. Patient remained intu­bated and ventilated for an additional 16 hours to per­mit clearing of secretions and the trachea got extu­bated the next morning. After extubation the ABG showed PaO 2 61, SaO 2 92% with FiO 2 0.5 [Table­ 1], he was maintaining BP 100/60 mmHg off dopam­ine ,hence was shifted to ward from ICU.

This patient then underwent right lung lavage after 4 days with 17 L of normal saline with same anaes­thetic management using Broncho-cath 37 F( Mallinckrodt) left endobronchial DLT. The proce­dure was conducted after performing a 20 minutes test of OLV of left lung. This time SaO 2 could be main­tained at 90% and above throughout the procedure.[Table 2] There were less haemodynamic, temperature and metabolic fluctuations during this lavage. The pro­cedure took 6&½ hours with total affluent saline of 17 L in 15 cycles, effluent fluid 15.5L and urine output 850 ml. Like the previous lavage, DLT was replaced with Portex cuffed single lumen endotracheal tube at the end of the procedure and the trachea was extu­bated the next morning after a good chest toilet and overnight ventilation.


   Discussion Top


Bronchopulmonary lavage, introduced by Ramirez in late 1960s is still the gold standard therapy for PAP [1] and is usually indicated in PAP only for pa­tients with significant symptoms and hypoxemia. With the patient under general anaesthesia, the lungs are usu­ally lavaged one at a time with 3 to 5 days between lavages. The technique has improved over years en­hancing effective removal of accumulated material in lungs. It has been recently shown that recombinant Granulocyte-Macrophage colony stimulating factor (GM-CSF) 5µg kg -1 day -1 for 6-12 weeks appears to benefit a subset of adult patients with PAP and may represent alternative to whole lung lavage in treating this disease. [1],[2] Few cases are reported to be benefited by plasmapheresis. [1],[3] Our patient had received GM­CSF therapy before reaching our institute but had failed to respond clinically. His WBC count was 75,000/ mm 3 with neutrophils 97% following GM-CSF therapy.

It is advised to lavage the more affected lung first for allowing better lung to provide gas exchange. Left lung is lavaged first in equal involvement of both lungs, leaving the larger right lung to support gas exchange during OLV [4] .We conducted BPL on left lung first as both the lungs of this patient were equally affected.

Preoxygenation for 5 minutes before induction is extremely important, not merely as a part of routine protocol; but because failure of denitrogenation of the lung leaves nitrogen bubbles in alveoli and limits the effectiveness of lavage.

Traditionally the lavage is conducted in lateral decubitus to lavage dependent lung and to ventilate the nondependent lung to minimize the risk of spillage of saline to other lung .But this is associated with higher ventilation perfusion mismatch in a already severely hypoxic patient Therefore, unlike the previous reports Beccaria et al [5] ventilated dependent lung and lavaged the nondependent one to give better ventilation perfu­sion ratio. Andrew Perez and colleagues have performed last part of the lavage in prone position specifically to clear the posterior segment of lungs. In their study of six patients, right lung lavage of one patient had to be terminated because of displacement of DLT in prone. [6] We performed the procedure in supine position with lateral tilt using a wedge to elevate the ventilated lung as it was conducted in the cumbersome ICU cubicle and not on the usual operating room table, and patient being somewhat haemodynamically unstable requiring inotropes.

Before starting lavage a 20 minutes test of one lung ventilation was performed with high inspiratory oxygen fraction up to 1 and low positive end- expira­tory pressure of 5 cm H 2 O while the other lung was actively deflated and degassed as much as possible in order to reproduce the worst possible condition that could occur during lavage. In this way safety of the procedure was tested before proceeding to lavage. Recently a less complicated procedure, bronchofi­berscopic lobar lavage under local anaesthesia has been proposed for carefully selected patients. Cheng and colleagues underline the fact that this procedure is safe and does not require anaesthetic support, how­ever it is recommended only in milder disease or con­versely in particularly severe cases in which the physi­ological derangement of whole lung lavage especially during drainage phase would not be tolerated by pa­tient which is revealed after 20 minutes test of one lung ventilation [4],[7]. In critically ill patients extra-corporal membrane oxygenation can be used to support gas exchange during lavage. [4],[8]

Infusion of large volumes of saline in lungs is as­sociated with mediastinal shift, increased intrathoracic pressure, CVP, Pulmonary capillary wedge pressure, arterial oxygen tension and hypotension. Despite the increase in CVP and PCWP it has been postulated that ventricular filling is not increased, and may be actually compromised following impaired venous return to the thorax of unknown etiology. [9] Arterial oxygen tension increases during filling because blood flow to nonventilated lung is decreased by the lavage fluid infu­sion pressure. Hypotension, rise in CVP and rise in SaO 2 were classically noticed in our patient.

Associated special problems during the proce­dure are displacement of the DLT and a leak through the DLT resulting in spillage of lavage fluid into the ventilated lung. That is why it is mandatory to confirm the placement of the DLT by fiberoptic broncho­scope. The procedure has to be terminated immedi­ately and the DLT can be replaced with single lumen ETT in case of sudden displacement. Continuous moni­toring to detect the loss of lung isolation was done as follows:

  1. The appearance of bubbles in the lavage fluid draining from the lavaged side.
  2. Increased resistance to ventilation and appearance of rales and rhonchi on the ventilated side.


During the procedure, all the measures should be taken to avoid hypothermia since the procedure takes several hours to complete and with use of lavage fluid of ambient temperature. Temperature of the patient was maintained using lavage fluid warmed to body tempera­ture, warming blanket and i.v. fluid warmer.

Though post lavage radiographs show partial clearing of PAP by 6 weeks compared with baseline pre-wash radiograph, pulmonary mechanics and gas exchange improve rapidly after the lavage. [10] SaO 2 of our patient improved from 92% with 0.5 FiO 2 to 96% on room air in four days after the lavage and was dis­charged home.

Our case report illustrates that the rare disor­der of Pulmonary Alveolar Protienosis can be suc­cessfully managed with technique of Whole Lung Lavage with a good teamwork between anaesthesiologist, chest physician, respitatory therapiest and intensivist.



 
   References Top

1.Ioachimescu OC and Kavuru MS.Chronic Pulmonary alveolar proteinosis. Chronic Respiratory Disease 2006; 3:149-159.  Back to cited text no. 1      
2.Kavuru Mani S, Bonfield Tracy L,Thomassen Mary J. Pulmonary Alveolar Proteinosis. Textbook of respira­tory medicine 4 th edition. Elsevier Saunders 2004;59: 1716-1734.  Back to cited text no. 2      
3.Kavuru Mani S, Bonfield Tracey L and Thomassen Mary J. Plasmapheresis, GM-CSF, and alveolar proteinosis. American Journal of Respiratory and Critical Care Medi­cine 2003;167:1036-1037.  Back to cited text no. 3      
4.Alfery david D, Benumof JL, Spragg RG.Anesthesia for Bronchopulmonary lavage. Thoracic Anesthesia by Kaplan Joel A, Churchill Livingston 1983 :403-417  Back to cited text no. 4      
5.Beccaria M, Luiseti M, Rodi G et al. Long term benefit after whole long lavage in pulmonary alveolar proteinosis. Eur Respir J 2004;23:526-531  Back to cited text no. 5      
6.Perez Andrew and. Rogers Robert M. Enhanced Alveo­lar Clearance with Chest Percussion Therapy and Posi­tional Changes During Whole-Lung Lavage for Alveo­lar Proteinosis . Chest 2004;125: 2351-2356.  Back to cited text no. 6      
7.Shih-Lung Cheng, Hou-Tai Chang, Lau Hon-Ping, Lee Li-Na, and Yang Pan-Chyr. Treatment by Bronchofiberscopic Lobar Lavage. Chest 2002; 122: 1480-1485.  Back to cited text no. 7      
8.Sihoe A D, Nq V M, Liu R W, Cheng LC.Pulmonary alveolar proteinosis in extremis: the case for aggressive whole lung lavage with extracorporeal membrane oxy­genation support. . Heart Lung Circ 2008;17:69-72.  Back to cited text no. 8      
9.Swenson JD, Astle KL, Bailey PL. Reduction in left ven­tricular filling during bronchopulmonary lavage dem­onstrated by transesophageal echocardiography. Anesth Analg 1995; 81:634-637.  Back to cited text no. 9      
10.Gale M E, Karlinsky J B, Robins AG. Bronchopulmonary lavage in Pulmonary Alveolar Proteinosis:Chest Radio­graph Observations. AJR : 1986;146: 981-985.  Back to cited text no. 10      


    Figures

  [Figure 1]
 
 
    Tables

  [Table 1], [Table 2]



 

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