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Aetna Aetna
Clinical Policy Bulletin:
Lung Transplantation
Number: 0598


Policy

  1. Aetna considers lung transplantation medically necessary for any of the following qualifying conditions for members who meet the transplanting institution's selection criteria.  In the absence of an institution's selection criteria, members must meet both the general selection criteria (see section on General Selection Criteria) and any applicable disease-specific selection criteria (see Disease-Specific Selection Criteria accompanying the list of Qualifying Conditions below):

    Qualifying Conditions for Lung Transplantation (not an all-inclusive list):

    1. Alpha1-antitrypsin deficiency: Persons who meet the emphysema/alpha1-antitrypsin deficiency disease-specific selection criteria below
    2. Broncho-pulmonary dysplasia
    3. Congenital heart disease (Eisenmenger's defect or complex): Persons who meet the disease-specific criteria for Eisenmenger's below
    4. Cystic fibrosis: Persons who meet the disease-specific selection criteria for cystic fibrosis
    5. Graft-versus-host disease or failed primary lung graft
    6. Lymphangioleiomyomatosis (LAM) with end-stage pulmonary disease
    7. Obstructive lung disease (e.g., bronchiectasis, bronchiolitis obliterans, chronic obstructive pulmonary disease (COPD), emphysema): For persons with pulmonary fibrosis, see the disease-specific selection criteria for pulmonary fibrosis below
    8. Primary pulmonary hypertension: Persons who meet the disease-specific selection criteria for primary pulmonary hypertension.
    9. Restrictive lung disease (e.g., allergic alveolitis, asbestosis, collagen vascular disease, desquamative interstitial fibrosis, eosinophilic granuloma, idiopathic pulmonary fibrosis, post-chemotherapy, sarcoidosis, and systemic sclerosis [scleroderma]): For persons with sarcoidosis, see the disease-specific selection criteria below.

    Disease-Specific Selection Criteria:

    1. Lung transplant for cystic fibrosis (CF) is considered medically necessary for persons who meet the general selection criteria for lung transplantation and exhibit at least 2 of the following signs and symptoms of clinical deterioration:

      1. Cycling intravenous antibiotic therapy
      2. Decreasing forced expiratory volume in 1 second (FEV1)
      3. Development of carbon dioxide (CO2) retention (pCO2 greater than 50 mm Hg)
      4. FEV1 less than 30 % predicted
      5. Increasing frequency of hospital admission
      6. Increasing severe exacerbation of CF -- especially an episode requiring hospital admission
      7. Initiation of supplemental enteral feeding by percutaneous endoscopic gastrostomy or parenteral nutrition
      8. Non-invasive nocturnal mechanical ventilation
      9. Recurrent massive hemoptysis
      10. Worsening arterial-alveolar (A-a) gradient requiring increasing concentrations of inspired oxygen (FiO2) 
    2. Lung transplant for emphysema (including alpha 1-antitrypsin deficiency) is considered medically necessary for persons who meet the general criteria for lung transplantation and both of the following clinical criteria:

      1. Hospitalizations for exacerbation of COPD associated with hypercapnia in the preceding year.  Hypercapnia is defined as pCO2 greater than or equal to 50 mm Hg with hospitalizations and/or the following associated factors:

        1. Declining body mass index
        2. Increasing oxygen requirements
        3. Reduced serum albumin
        4. Presence of cor pulmonale (defined as clinical diagnosis by a physician or any 2 of the following:

          1. enlarged pulmonary arteries on chest X-ray  
          2. mean pulmonary artery pressure by right heart catheterization of greater than 25 mm Hg at rest or 30 mm Hg with exercise
          3. pedal edema or jugular venous distention
          4. right ventricular hypertrophy or right atrial enlargement on EKG
      2. FEV1 less than 30% predicted.

    3. Lung transplant for Eisenmenger's complex is considered medically necessary for persons who meet the general criteria for lung transplantation and any of the following disease-specific criteria:

      1. Marked deterioration in functional capacity (New York Heart Association (NYHA) Class III) 
      2. Pulmonary hypertension with mean pulmonary artery pressure by right heart catheterization greater than 25 mm Hg at rest or 30 mm Hg with exercise
      3. Signs of right ventricular failure -- progressive hepatomegaly, ascites.
    4. Lung transplant for pulmonary fibrosis is considered medically necessary for persons who meet the general criteria for lung transplantation and any of the following disease-specific criteria:

      1. Diffusing capacity for carbon monoxide (DLCO) less than 60 % predicted
      2. Presence of cor pulmonale (indicative of severe pulmonary fibrosis) or pulmonary hypertension
      3. Total lung capacity (TLC) less than 70 % predicted.
    5. Lung transplant for pulmonary hypertension is considered medically necessary for persons who meet the general criteria for lung transplantation plus any of the following criteria, and valvular disease has been excluded by echocardiography:

      1. Persons who are NYHA III, failing conventional vasodilators (calcium channel blockers or endothelin receptor antagonists)
      2. Persons who are NYHA III, and have initiated or being considered for initiation of parenteral or subcutaneous vasodilator therapy
      3. Pulmonary hypertension with mean pulmonary artery pressure by right heart catheterization of greater than 25 mm Hg at rest or 30 mm Hg with exercise, or pulmonary artery systolic pressure of 50 mm Hg or more defined by echocardiography or pulmonary angiography.

      Note: NYHA Class III for heart failure is defined as follows:

      Persons with cardiac disease resulting in marked limitation of physical activity.  They are comfortable at rest.  Less than ordinary activity (i.e., mild exertion) causes fatigue, palpitation, dyspnea, or anginal pain.

    6. Lung transplant for sarcoidosis is considered medically necessary for persons who meet the general criteria for lung transplantation plus any of the following disease-specific criteria:

      1. DLCO less than 60 % predicted
      2. Presence of cor pulmonale (indicative of severe pulmonary fibrosis) or pulmonary hypertension
      3. Total lung capacity less than 70 % predicted.

    General Selection Criteria:

    The member must meet the transplanting institution's selection criteria.  In the absence of an institution's selection criteria, all of the following selection criteria must be met, and none of the contraindications listed below should be present:

    1. Absence of acute or chronic active infection (pulmonary or non-pulmonary) that is not adequately treated; and
    2. Adequate cardiac status (e.g., no angiographic evidence of significant coronary artery disease, ejection fraction greater than 40 %, no myocardial infarction in last 6 months, negative stress test).  Persons with any cardiac symptoms may require heart catheterization to rule out significant heart disease; and
    3. Adequate functional status.  Under established guidelines, active rehabilitation is considered important to the success of transplantation.  Mechanically-ventilated or otherwise immobile persons are considered poor candidates for transplantation; and
    4. Adequate liver and kidney function, defined as a bilirubin of less than 2.5 mg/dL and a creatinine clearance of greater than 50 ml/min/kg; and
    5. Limited life expectancy of less than 2 years; and
    6. No active alcohol or chemical dependency that interferes with compliance to a strict treatment regimen.  Persons with a history of drug or alcohol abuse must be abstinent for at least 3 months before being considered an eligible transplant candidate; and
    7. No uncontrolled and/or untreated psychiatric disorders that interfere with compliance to a strict treatment regimen; and
    8. Absence of inadequately controlled HIV/AIDS infection, defined as 
      1. CD4 count greater than 200 cells/mm3 for greater than 6 months; and
      2. HIV-1 RNA (viral load) undetectable; and
      3. No other complications from AIDS, such as opportunistic infection (e.g., aspergillus, tuberculosis, coccidioidomycosis, resistant fungal infections) or neoplasms (e.g., Kaposi's sarcoma, non-Hodgkin's lymphoma); and
      4. On stable antiviral therapy greater than 3 months.

    Contraindications: Lung transplantation is considered experimental and investigational for persons with the following contraindications to lung transplant surgery because the safety and effectiveness of lung transplantation in persons with these contraindications has not been established:

    1. Malignancy involving the lung (primary or metastatic).  Persons with a history of non-pulmonary cancer must be in remission before being considered a lung transplant candidate.  Note: Because of disappointing results, lung transplantation is considered experimental and investigational as a treatment for bronchioloalveolar carcinoma.
    2. Multi-system disease.  Persons with potentially multi-system diseases such as systemic sclerosis (scleroderma), other collagen vascular diseases such as systemic lupus erythematosus, or sarcoidosis must be carefully evaluated to ensure that their disease is primarily confined to the lung.  Persons with diabetes must be carefully evaluated to rule out significant diabetic complications such as nephropathy, neuropathy or retinopathy.
    3. Other effective medical treatments or surgical options are available.
    4. Presence of gastrointestinal disease (e.g., bleeding peptic ulcer, chronic hepatitis, diverticulitis).
    5. Refractory uncontrolled hypertension.
    6. Single-lung transplantation is contraindicated in persons with chronic pulmonary infections (e.g., bronchiectasis, chronic bronchitis, and cystic fibrosis)
    7. Smoking.  Persons with a history of smoking must be abstinent for 6 months before being considered eligible for lung transplantation. 
  2. Aetna considers lobar (from living-related donors or cadaver donors) lung transplantation medically necessary for persons with end-stage pulmonary disease when selection criteria are met (see above).

  3. Aetna considers lung xenotransplantation (e.g., porcine xenografts) experimental and investigational for any pulmonary conditions because of insufficient evidence in the peer-reviewed literature.

  4. Aetna considers prophylactic anti-reflux surgery to improve lung function and survival in lung transplant recipients without gastroesophageal reflux disease as experimental and investigational because of insufficient evidence in the peer-reviewed literature.

  5. Aetna considers the TransMedics Organ Care System for preservation and transport of donor lungs experimental and investigational because its effectiveness has not been established.

See also CPB 0597 - Heart-Lung Transplant.



Background

Lung transplantation (LTX) has become a viable treatment option for carefully selected patients with end-stage pulmonary disease (ESPD).  Single, double, and lobar-lung transplantation have all been performed successfully for a variety of diseases.  Single-LTX appears to be most effective for patients with end-stage pulmonary fibrosis, while double-LTX is most effective for patients with end-stage chronic obstructive pulmonary disease (COPD) and cystic fibrosis (CF) in whom cardiac function has been preserved.  Lobar-LTX (from living donors or cadaver donors) is usually reserved for children or adolescents who are appropriate candidates for LTX and will not survive waiting for cadaver lungs.  Indications for LTX in pediatric patients include pulmonary vascular disease, bronchiolitis obliterans, broncho-pulmonary dysplasia, graft failure due to viral pneumonitis, and CF.

Chronic obstructive pulmonary disease and alpha 1-antitrypsin deficiency, the 2 principal causes of emphysema, are responsible for approximately 60 % of all single-LTX performed.  Other indications for single-LTX include primary pulmonary hypertension, Eisenmenger's syndrome, as well as a variety of interstitial lung diseases (e.g., interstitial pulmonary fibrosis).

Cystic fibrosis, emphysema, and alpha 1-antitrypsin deficiency are the most common indications for double-LTX, also known as bilateral single-LTX (sequential replacement of both lungs).  Comparing patients who have undergone en bloc double-LTX to patients who have undergone bilateral single-LTX, studies have shown a better outcome for those who have undergone the bilateral sequential procedure.  The latter is generally considered the procedure of choice for patients with any pulmonary disorder complicated by chronic airway infection, such as bronchiectasis, CF, and chronic bronchitis.  The possibility of spillover of infection from the native lung to the allograft precludes single-LTX in such patients.

Although LTX offers acceptable prospects for 5-year survival, chronic rejection and donor shortage remain to be major problems.  To address the problem of donor shortage, living-donor lobar-LTX has been performed with satisfactory intermediate survival and functional results.  In lobar-LTX, a lobe of the donor's lung is excised, sized appropriately for the recipient, and transplanted.  Common indications for living-donor bilateral lobar-LTX are CF and severe primary pulmonary hypertension.  Based on available scientific evidence, there is no significant difference in effectiveness between living-donor lobar-LTX and cadaver lobar-LTX.

There are currently 2 surgical therapies for the treatment of end-stage emphysema: LTX and lung volume reduction surgery (LVRS) (see CPB 0160 - Lung Volume Reduction Surgery).  Ideal candidates for LVRS are those with hyper-inflation, heterogeneous distribution of disease, forced expiratory volume in 1 second (FEV1) of more than 20 %, and normal PCO2.  Patients with diffuse disease, low FEV1, hypercapnia, and associated pulmonary hypertension are directed toward transplantation.  Moreover, LTX provides more satisfactory results than LVRS for patients with emphysema due to alpha1-antitrypsin deficiency.  Combinations of LTX and LVRS, simultaneously or sequentially, are feasible but rarely indicated.

Complications of LTX include re-implantation response and airway complications.  Rejection may occur in the hyper-acute, acute, or chronic settings and requires judicious management with immunosuppression.  Infection and malignancy remain potential complications of the commitment to lifelong systemic immunosuppression.  Obese (greater than 20 % of ideal body weight), cachectic (less than 80 % of ideal body weight), mechanically ventilated or otherwise immobile patients are considered poor candidates for transplantation.

There is a steadily increasing need for a greater supply of lung donors.  Xenotransplantation offers the possibility of an unlimited supply of lungs that could be readily available when needed.  However, antibody-mediated mechanisms cause the rejection of pig organs transplanted into non-human primates, and these mechanisms provide key immunological barriers that have yet to be overcome.  Although porcine hearts have functioned in heterotopic sites in non-human primates for periods of several weeks, no transplanted porcine lung has functioned for even 24 hours.  Currently, lung xenotransplantation is not a clinically applicable option, and is therefore considered an experimental and investigational procedure.

Amital and colleagues (2008) noted that LTX impairs surfactant activity, which may contribute to primary graft dysfunction (PGD).  In an open, randomized, controlled prospective study, these researchers examined if the administration of surfactant during transplantation serves as an effective preventive measure.  A total of 42 patients scheduled for single (n = 38) or double (n = 4) LTX were randomly assigned to receive, or not, intra-operative surfactant treatment.  In the treated group, bovine surfactant was administered at a dose of 20 mg phospholipids/kg body weight through bronchoscope after the establishment of bronchial anastomosis.  The groups were compared for oxygenation (PaO2/FiO2), chest X-ray findings, PGD grade, and outcome.  Compared with the untreated group, patients who received surfactant were characterized by better post-operative oxygenation mean PaO2/FiO2 (418.8 +/- 123.8 versus 277.9 +/- 165 mm Hg, p = 0.004), better chest radiograph score, a lower PGD grade (0.66 versus 1.86, p = 0.005), fewer cases of severe PGD (1 patient versus 12, p < 0.05), earlier extubation (by 2.2 hrs; 95 % confidence interval (CI): 1.1 to 4.3 hrs, p = 0.027), shorter intensive care unit stay (by 2.3 days; 95 % CI: 1.47 to 3.74 days, p = 0.001), and better vital capacity at 1 month (61 % versus 50 %, p = 0.022).  One treated and 2 untreated patients died during the first post-operative month.  The authors concluded that surfactant instillation during LTX improves oxygenation, prevents PGD, shortens intubation time, and enhances early post-transplantation recovery.  Moreover, they stated that further, larger studies are needed to evaluate if surfactant should be used routinely in LTX.

In LTX recipients, gastro-esophageal reflux disease (GERD) is associated with increased incidence of acute rejection, earlier onset of chronic rejection, and higher mortality.  Surgical treatment of GERD in LTX recipients seems to prevent early allograft dysfunction and improve overall survival.  A total (360 degrees) fundoplication is shown to be a safe and effective method for treating GERD in LTX recipients for this high-risk patient population.  The principal goal should be to minimize reflux of enteric contents that may lead to micro- or macro-aspiration events in this complicated group of patients.  Peri-operative care should involve a multi-disciplinary approach, including physicians and other health care providers familiar with the complexities of LTX recipients (Hartwig et al, 2005).

Molina et al (2009) identified outcomes in LTX recipients with clinical evidence of GERD.  Retrospective review of 162 LTX recipients at the authors' institution between January 1994 and June 2006 was performed.  Gastro-esophageal reflux disease was confirmed in symptomatic patients by esophago-gastro-duodenoscopy (EGD) and/or esophagography.  Occurrence of biopsy-proven obliterative bronchiolitis (OB) and bronchiolitis obliterans syndrome (BOS) were analyzed.  Kaplan-Meier analysis of survival and Cox proportional hazard analysis of risk factors were performed.  Gastro-esophageal reflux disease was diagnosed in 21 (13 %) of patients, usually following LTX (71 %).  There was no difference in mean survival (1,603 +/- 300 versus 1,422 +/- 131 days; log rank p > 0.05), or development of OB (5 % versus 6 %, respectively; p > 0.05) in patients with GERD compared with patients without GERD.  However, there was correlation between GERD and BOS (p = 0.01).  The authors concluded that symptomatic GERD is increased following LTX.  Patients with symptomatic GERD demonstrated an increased incidence of BOS, but survival was not affected in this study.  They stated that more sensitive and specific diagnostic tools should be implemented in all LTX recipients to investigate the impact of symptomatic and silent GERD and thus improve outcomes after LTX.

Burton et al (2009) stated that GERD in LTX recipients has gained increasing attention as a factor in allograft failure.  There are few data on the impact of fundoplication on survival or lung function, and less on its effect on symptoms or quality of life.  Patients undergoing fundoplication following LTX from 1999 to 2005 were included in the study.  Patient satisfaction, changes in GERD symptoms, and the presence of known side effects were assessed.  The effect on lung function, body mass index, and rate of progression to the BOS were recorded.  A total of 21 patients (13 males), in whom reflux was confirmed on objective criteria, were included, with a mean age of 43 years (range of 20 to 68).  Time between transplantation and fundoplication was 768 days (range of 145 to 1,524).  The indication for fundoplication was suspected micro-aspiration in 13 and symptoms of GERD in 8.  There was 1 peri-operative death, at day 17.  There were 3 other late deaths.  Fundoplication did not appear to affect progression to BOS stage 1, although it may have slowed progression to stage 2 and 3.  Forced expiratory volume-1 % predicted was 72.9 (20.9), 6 months prior to fundoplication and 70.4 (26.8), 6 months post-fundoplication, p = 0.33.  Body mass index decreased significantly in the 6 months following fundoplication (23 kg/m(2) versus 21 kg/m(2), p = 0.05).  Patients were satisfied with the outcome of the fundoplication (mean satisfaction score 8.8 out of 10).  Prevalence of GERD symptoms decreased significantly following surgery (11 of 14 versus 4 of 17, p = 0.002).  Fundoplication does not reverse any decline in lung function when performed at a late stage post-LTX in patients with objectively confirmed GERD.  It may, however, slow progression to the more advanced stages of BOS.  Reflux symptoms were well-controlled and patients were highly satisfied.  The authors stated that whether performing fundoplication early post-LTX in selected patients can prevent BOS and improve long-term outcomes requires formal evaluation.

King et al (2009) examined the relationship between BOS and GERD measured by esophageal impedance.  After the initiation of routine screening for GERD, 59 LTX recipients underwent ambulatory esophageal impedance monitoring.  Exposure to acid reflux and non-acid liquid reflux was recorded.  Clinical outcomes were reviewed to analyze any effect of reflux on the time to development of BOS.  A total of 37 patients (65 %) had abnormal acid reflux and 16 (27 %) had abnormal non-acid reflux.  There was no relationship between acid reflux and BOS.  The hazard ratio (HR) for development of BOS in the presence of abnormal non-acid reflux was 2.8 (p = 0.043).  The HR for development of BOS increased to 3.6 (p = 0.022) when the number of acute rejection episodes was also taken into account.  The authors concluded that GERD is prevalent in LTX recipients and may represent a modifiable risk factor for BOS.  This study found non-acid reflux, measured by esophageal impedance to be associated with the development of BOS.  They stated that prospective studies are now needed to investigate a causal association between GERD and the development of BOS and to establish the role of surgery for GERD in preventing progression to BOS.

Robertson et al (2010) noted that LTX is an accepted treatment strategy for end-stage lung disease; however, BOS is a major cause of morbidity and mortality.  These investigators reviewed the role of GERD in BOS and the evidence suggesting the benefits of anti-reflux surgery in improving lung function and survival.  There is a high prevalence of gastro-esophageal reflux in patients post-LTX.  This may be due to a high pre-operative incidence, vagal damage and immunosuppression.  Reflux in these patients is associated with a worse outcome, which may be due to micro-aspiration.  Anti-reflux surgery is safe in selected LTX recipients; however there has been 1 report of a post-operative mortality.  Evidence is conflicting but may suggest a benefit for patients undergoing anti-reflux surgery in terms of lung function and survival; there are no controlled studies.  The precise indications, timing, and choice of fundoplication are yet to be defined, and further studies are required.

Zheng et al (2011) examined the safety and possible benefits of laparoscopic anti-reflux surgery in pediatric patients following LTX and heart-lung transplantation.  An Institutional Review Board-approved retrospective chart review was performed to evaluate the outcomes and complications of laparoscopic anti-reflux surgery in pediatric LTX  and heart-lung transplant patients.  Spirometry data were collected for BOS staging using BOS criteria for children.  A total of 25 LTX and heart-lung transplants were performed between January 2003 and July 2009.  Eleven transplant recipients, including 6 double-lung and 5 heart-lung, with a median age of 11.7 years (range of 5.1 to 18.4 years), underwent a total of 12 laparoscopic Nissen fundoplications at a median of 427 days after transplant (range of 51 to 2310 days).  The diagnosis of GERD was made based upon clinical impression, pH probe study, gastric emptying study, and/or esophagram in all patients.  Three patients already had a gastrostomy tube in place and 2 had one placed at the time of fundoplication.  There were no conversions to open surgery, 30-day re-admissions, or 30-day mortalities.  Complications included 1 exploratory laparoscopy for free air 6 days after laparoscopic Nissen fundoplication for a gastric perforation that had spontaneously sealed.  Another patient required a revision laparoscopic Nissen 822 days following the initial fundoplication for a para-esophageal hernia and recurrent GERD.  The average length of hospital stay was 4.4 +/- 1.7 days.  Nine of the 12 fundoplications were performed in patients with baseline spirometry values prior to fundoplication and who could also complete spirometry reliably.  One of these 9 operations was associated with improvement in BOS stage 6 months after fundoplication; 7 were associated with no change in BOS stage; and 1 was associated with a decline in BOS stage.  The authors concluded that it is feasible to perform laparoscopic Nissen fundoplication in pediatric LTX and heart-lung transplant recipients without mortality or significant morbidity for the treatment of GERD.  The real effect on pulmonary function can not be assessed due to the small sample size and lack of reproducible spirometry in the younger patients.  The authors stated that additional studies are needed to elucidate the relationship between anti-reflux surgery and the potential for improving pulmonary allograft function and survival in children that has been previously observed in adult patients.

Robertson et al (2012) evaluated the safety of fundoplication in LTX recipients and its effects on quality of life.  Between June 1, 2008 and December 31, 2010, a prospective study of LTX recipients undergoing fundoplication was undertaken.  Quality of life was assessed before and after surgery.  Body mass index (BMI) and pulmonary function were followed-up.  A total of 16 patients, mean +/- SD age of 38 +/-11.9 yrs, underwent laparoscopic Nissen fundoplication.  There was no peri-operative mortality or major complications.  Mean +/- SD hospital stay was 2.6 +/- 0.9 days; 15 out of 16 patients were satisfied with the results of surgery post-fundoplication.  There was a significant improvement in reflux symptom index and DeMeester questionnaires and gastro-intestinal quality of life index scores at 6 months.  Mean BMI decreased significantly after fundoplication (p = 0.01).  Patients operated on for deteriorating lung function had a statistically significant decrease in the rate of lung function decline after fundoplication (p = 0.008).  The authors concluded that laparoscopic fundoplication is safe in selected LTX recipients.  Patient benefit is suggested by improved symptoms and satisfaction.  Thye stated that this procedure is acceptable, improves quality of life and may reduce deterioration of lung function.  These preliminary findings need to be validated by well-designed studies.

Fisichella and colleagues (2012) hypothesized that laparoscopic anti-reflux surgery (LARS) alters the pulmonary immune profile in LTX patients with GERD.  In 8 LTX patients with GERD, these researchers quantified and compared the pulmonary leukocyte differential and the concentration of inflammatory mediators in the broncho-alveolar lavage fluid (BALF) 4 weeks before LARS, 4 weeks after LARS, and 12 months after LTX.  Freedom from BOS (graded 1 to 3 according to the International Society of Heart and Lung Transplantation guidelines), FEV1 trends, and survival were also examined.  At 4 weeks after LARS, the percentages of neutrophils and lymphocytes in the BALF were reduced (from 6.6 % to 2.8 %, p = 0.049, and from 10.4 % to 2.4 %, p = 0.163, respectively).  The percentage of macrophages increased (from 74.8 % to 94.6 %, p = 0.077).  Finally, the BALF concentration of myeloperoxide and interleukin-1-beta tended to decrease (from 2,109 to 1,033 U/mg, p = 0.063, and from 4.1 to 0 pg/mg protein, p = 0.031, respectively), and the concentrations of interleukin-13 and interferon-gamma tended to increase (from 7.6 to 30.4 pg/mg protein, p = 0.078 and from 0 to 159.5 pg/mg protein, p = 0.031, respectively).  These trends were typically similar at 12 months after transplantation.  At a mean follow-up of 19.7 months, the survival rate was 75 % and the freedom from BOS was 75 %.  Overall, the FEV1 remained stable during the first year after transplantation.  The authors concluded that these preliminary findings indicated that LARS can restore the physiologic balance of pulmonary leukocyte populations and that the BALF concentration of pro-inflammatory mediators is altered early after LARS.  These results suggested that LARS could modulate the pulmonary inflammatory milieu in LTX patients with GERD.

There is great disparity between the supply of donor lungs and the number of potential lung transplant recipients.  The shortage of donor lungs for transplantation demands optimal utilization of the donor organ.  For many years hypothermic preservation has been the universal standard for organ preservation.  Although limited in terms of the duration of preservation, hypothermic preservation has had the major advantages of simplicity, portability and affordability.  Recently, organ preservation and transportation by normothermic perfusion has been reported to be superior over static cold storage in experimental settings; however, all devices examined were non-portable.  The Organ Care System (TransMedics, Inc., Andover, MA) is a portable device for preservation and transport of donor lungs.  However, its role in lung transplantation has not yet been established.

Van Raemdonck et al (2010) noted that the critical organ shortage has forced lung transplant teams to extend their donor criteria, thereby compromising a good early outcome in the recipient.  Better preservation solutions for longer storage are welcomed to further reduce incidence of primary graft dysfunction.  New ex-vivo techniques to assess and to condition lungs prior to transplantation are hoped to increase the number of available pulmonary grafts.  Although no prospective clinical trial has been carried out so far, clinical and experimental evidence suggest that an extracellular solution is currently the preservation fluid of choice for lung transplantation.  The combination of an antegrade and retrograde pulmonary flush and technique to control reperfusion and ventilation are becoming common practice, although the evidence to support this method is low.  Ex-vivo lung perfusion to assess and to re-condition lungs has been demonstrated to be well-tolerated and effective in small clinical series.  The author concluded that new extracellular preservation solutions have contributed in decreasing the incidence of primary graft dysfunction over the last decade leaving more room to extend the donor criteria and ischemic time.  Ex-vivo lung perfusion is now on the horizon as a potential method to prolong the preservation time and to resuscitate lungs of inferior quality.

Warnecke et al (2012) stated that cold flush and static cold storage is the standard preservation technique for donor lungs before transplantations.  Several research groups have assessed normothermic perfusion of donor lungs but all devices investigated were non-portable.  In a pilot study, these investigators reported first-in-man experience of the portable Organ Care System (OCS) Lung device for concomitant preservation, assessment, and transport of donor lungs.  Between Feb 18, and July 1, 2011, 12 patients were transplanted at 2 academic lung transplantation centers in Hanover, Germany and Madrid, Spain.  Lungs were perfused with low-potassium dextran solution, explanted, immediately connected to the OCS Lung, perfused with Steen's solution supplemented with 2 red-cell concentrates.  These researchers assessed donor and recipient characteristics and monitored extended criteria donor lung scores; primary graft dysfunction scores at 0, 24, 48, and 72 hrs; time on mechanical ventilation after surgery; length of stays in hospital and the intensive-care unit after surgery; blood gases; and survival of grafts and patients.  Eight donors were female and 4 were male (mean age of 44.5 years, range of 14 to 72).  Seven recipients were female and 5 were male (mean age of 50.0 years, range of 31 to 59).  The pre-harvest donor ratio of partial pressure of oxygen (PaO(2)) to fractional concentration of oxygen in inspired air (F(I)O(2)) was 463.9 (SD 91.4).  The final ratio of PaO(2) to F(I)O(2) measured with the OCS Lung was 471.58 (127.9).  The difference between these ratios was not significant (p = 0.72).  All grafts and patients survived to 30 days; all recipients recovered and were discharged from hospital.  The authors concluded that lungs can be safely preserved with the OCS Lung, resulting in complete organ use and successful transplantation in this series of high-risk recipients.  In November, 2011, the authors began recruitment for a prospective, randomized, multi-center trial (INSPIRE) to compare preservation with OCS Lung with standard cold storage.

Also, an UpToDate review on “Lung transplantation: Donor lung preservation” (Cypel et al, 2012) states that “The cold static preservation system described above was developed in an era with younger organ donors and good-quality organs.  However, in order to increase the availability of donor organs, older and sometimes injured donor organs are being used.  The use of suboptimal donor lungs and difficulties assessing lung function in donation after cardiac death have made it necessary to explore alternative preservation techniques.  Hypothermic preservation inhibits cellular metabolism and eliminates the possibility of substantial reparative processes occurring after donor organ injury.  For this reason, normothermic (37º C) or near-normothermic (25 to 34º C) ex vivo perfusion is becoming popular as a preservation alternative in kidney and liver transplantation.  Attempts at using a ventilating and perfusing machine for lung preservation have failed in the past, largely due to the development of lung edema and increases in pulmonary vascular resistance.  However, investigators have used an animal model to develop a perfusion system that allows evaluation of lung function ex vivo.  A key part of ex vivo perfusion is the identification of a specific solution (Steen® solution) that allows for ex vivo perfusion of lungs without development of pulmonary edema.  In an animal model and a single human case, after a short period (60 to 90 minutes) of ex vivo evaluation, lungs were successfully transplanted.  An acellular, ex vivo lung perfusion (EVLP) technique that can maintain donor lungs for at least 12 hours at body temperature without inducing injury has been tested in porcine and human lungs.  After prolonged EVLP, lung function after transplantation was excellent.  Using this acellular perfusion technique also allowed evaluation of lung function ex vivo.  However, another animal model of EVLP was less successful; six hours of EVLP resulted in impaired lung function, manifest by increased pulmonary vascular resistance (PVR) and increased airway pressures towards the end of the procedure.  A clinical trial is underway using normothermic ex vivo lung perfusion as a method to reassess and optimize donor lungs that are initially unsuitable for transplantation”.

TramsMedics is currently conducting a clinical trial “International Randomized Study of the TransMedics Organ Care System (OCS Lung) for Lung Preservation and Transplantation (INSPIRE)”, which compares preservation of donor lungs using OCS-Lung perfusion device to cold flush and storage (last verified December 2012).  http://clinicaltrials.gov/show/NCT01630434.

 
CPT Codes / HCPCS Codes / ICD-9 Codes
CPT codes covered if selection criteria are met:
32850
32851
32852
32853
32854
CPT codes not covered for indications listed in the CPB:
43257
43280
43281
43282
43325
43327
43328
43332
43333
43334
43335
43336
43337
ICD-9 codes covered if selection criteria are met:
135 Sarcoidosis [must be carefully evaluated to ensure diseases is primarily confined to lung]
273.4 Alpha-1-antitrypsin deficiency
277.00 - 277.09 Cystic fibrosis [contraindicated for single-lung transplant]
277.89 Other specified disorders of metabolism [eosinophilic granuloma]
279.50 - 279.53 Graft-versus-host disease
416.0 Primary pulmonary hypertension
446.20 - 446.29 Hypersensitivity angitis [must be carefully evaluated to ensure diseases is primarily confined to lung]
491.2 Obstructive chronic bronchitis [contraindicated for single-lung]
491.8 Other chronic bronchitis [contraindicated for single-lung]
492.8 Other emphysema
494.0 - 494.1 Bronchiectasis [contraindicated for single-lung]
495.4 - 495.9 Extrinsic allergic alveolitis
496 Chronic airway obstruction, not elsewhere classified
501 Asbestosis
515 Post-inflammatory pulmonary fibrosis
516.3 Idiopathic fibrosing alveolitis
516.4 Lymphangioleiomyomatosis [with end-stage pulmonary disease]
517.2 Lung involvement in systemic sclerosis [must be carefully evaluated to ensure diseases is primarily confined to lung]
517.8 Lung involvement in other diseases classified elsewhere
745.4 Ventricular septal defect [Eisenmenger's defect or complrx]
748.4 Congenital cystic lung
748.5 Agenesis, hypoplasia, and dysplasia of lung
748.61 Congenital bronchiectasis
770.7 Chronic respiratory disease arising in the perinatal period [bronchopulmonary dysplasia]
996.84 Complications of transplanted organ, lung
Other ICD-9 codes related to the CPB:
140.0 - 239.9 Neoplasms [non-pulmonary cancer must be in remission before consideration]
305.1 Tobacco use disorder [must be abstinent for 6 months before consideration]
416.9 Chronic pulmonary heart disease, unspecified [cor pulmonale]
428.0 Congestive heart failure, unspecified [right ventricular]
429.3 Cardiomegaly [right ventricular hypertrophy or right atrial enlargement]
780.79 Other malaise and fatigue
783.21 Abnormal loss of weight
785.1 Palpitations
786.09 Other dyspnea and respiratory abnormalities
786.30 Hemoptysis, unspecified
786.31 Acute idiopathic pulmonary hemorhage in infants [AIPHI]
786.39 Other hemoptysis
786.51 Precordial pain
789.1 Hepatomegaly
789.5 Ascites
799.0 Asphyxia
V15.82 History of tobacco use [must be abstinent for 6 months before consideration]
V42.6 Organ or tissue replaced by transplant, lung
V46.0 - V46.2 Other dependence on machines, aspirator, respirator, or supplemental oxygen
ICD-9 codes contraindicated for this CPB (not all-inclusive):
001.0 - 139.8 Infectious and parasitic diseases [acute or chronic active infection not adequately treated including HIV/AIDS and complications such as aspergillus, tuberculosis, coccidoidomycosis, or fungal]
162.2 - 162.9 Malignant neoplasm of bronchus and lung
176.0 - 176.9 Kaposi's sarcoma [complication from AIDS]
197.0 Secondary malignant neoplasm of lung
202.00 - 202.98 Non-Hodgkin's lymphoma [complication from AIDS]
231.0 Carcinoma in situ of bronchus and lung
250.40 - 250.43 Diabetes mellitus with renal manifestations
250.50 - 250.53 Diabetes mellitus with ophthalmic manifestations
250.40 - 250.43 Diabetes mellitus with neurologic manifestations
290.0 - 319 Mental disorders [uncontrolled and/or untreated that interfere with compliance including alcohol, chemical, or tobacco dependency]
401.0 - 401.9 Essential hypertension [refractory uncontrolled]
410.00 - 412 Myocardial infarction [in last 6 months]
414.00 - 414.06 Coronary atherosclerosis [significant]
531.00 - 533.91 Gastic ulcer
562.01 - 562.13 Diverticula of intestine
571.40 - 571.49 Chronic hepatitis
710.0 Systemic lupus erythematosus [must be carefully evaluated to ensure diseases is primarily confined to lung]
V10.11 Personal history of malignant neoplasm of bronchus and lung
There is no specific code for the TransMedics Organ Care System:


The above policy is based on the following references:
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  9. Cooper DK, Keogh AM, Brink J, et al. Report of the Xenotransplantation Advisory Committee of the International Society for Heart and Lung Transplantation: The present status of xenotransplantation and its potential role in the treatment of end-stage cardiac and pulmonary diseases. J Heart Lung Transplant. 2000;19(12):1125-1165.
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  15. Starnes VA, Barr ML, Schenkel FA, et al. Experience with living-donor lobar transplantation for indications other than cystic fibrosis. J Thorac Cardiovasc Surg. 1997;114(6):917-922.
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  17. Cohen RG, Barr ML, Schenkel FA, et al. Living-related donor lobectomy for bilateral lobar transplantation in patients with cystic fibrosis. Ann Thorac Surg. 1994;57(6):1423-1428.
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  22. Kelly J, Moss J. Lymphangioleiomyomatosis. eMedicine Pulmonology Topic 1348. Omaha, NE: eMedicine.com; updated December 31, 2001. Available at: http://www.emedicine.com/med/topic1348.htm. Accessed September 25, 2003.
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  24. Starnes VA, Bowdish ME, Woo MS, et al. A decade of living lobar lung transplantation: Recipient outcomes. J Thorac Cardiovasc Surg. 2004;127(1):114-122.
  25. Barlesi F, Doddoli C, Gimenez C, et al. Bronchioloalveolar carcinoma: Myths and realities in the surgical management. Eur J Cardiothorac Surg. 2003;24(1):159-164.
  26. Cox A, Zhong R. Current advances in xenotransplantation. Hepatobiliary Pancreat Dis Int. 2005;4(4):490-494.
  27. Raz DJ, He B, Rosell R, Jablons DM. Bronchioloalveolar carcinoma: A review. Clin Lung Cancer. 2006;7(5):313-322.
  28. National Institute for Health and Clinical Excellence (NICE). Living-donor lung transplantation for end-stage lung disease. Interventional Procedure Guidance 170. London, UK: NICE; 2006.
  29. Schuurman HJ, Pierson RN 3rd. Progress towards clinical xenotransplantation. Front Biosci. 2008;13:204-220.
  30. Date H, Yamane M, Toyooka S, et al. Current status and potential of living-donor lobar lung transplantation. Front Biosci. 2008;13:1433-1439.
  31. Amital A, Shitrit D, Raviv Y, et al. The use of surfactant in lung transplantation. Transplantation. 2008;86(11):1554-1559.
  32. Fan Y, Xiao YB, Weng YG. Tacrolimus versus cyclosporine for adult lung transplant recipients: A meta-analysis. Transplant Proc. 2009;41(5):1821-1824.
  33. Groves S, Galazka M, Johnson B, et al. Inhaled cyclosporine and pulmonary function in lung transplant recipients. J Aerosol Med Pulm Drug Deliv. 2010;23(1):31-39.
  34. Huddleston CB. Lung transplantation for pulmonary hypertension in children. Pediatr Crit Care Med. 2010;11(2 Suppl):S53-S56.
  35. Hartwig MG, Appel JZ, Davis RD. Antireflux surgery in the setting of lung transplantation: Strategies for treating gastroesophageal reflux disease in a high-risk population. Thorac Surg Clin. 2005;15(3):417-427.
  36. Molina EJ, Short S, Monteiro G, et al. Symptomatic gastroesophageal reflux disease after lung transplantation. Gen Thorac Cardiovasc Surg. 2009;57(12):647-653.
  37. Burton PR, Button B, Brown W, et al. Medium-term outcome of fundoplication after lung transplantation. Dis Esophagus. 2009;22(8):642-648.
  38. King BJ, Iyer H, Leidi AA, Carby MR. Gastroesophageal reflux in bronchiolitis obliterans syndrome: A new perspective. J Heart Lung Transplant. 2009;28(9):870-875.
  39. Robertson AG, Ward C, Pearson JP, et al. Lung transplantation, gastroesophageal reflux, and fundoplication. Ann Thorac Surg. 2010;89(2):653-660.
  40. Zheng C, Kane TD, Kurland G, et al. Feasibility of laparoscopic Nissen fundoplication after pediatric lung or heart-lung transplantation: Should this be the standard? Surg Endosc. 2011;25(1):249-254.
  41. Robertson AG, Krishnan A, Ward C, et al. Anti-reflux surgery in lung transplant recipients: Outcomes and effects on quality of life. Eur Respir J. 2012;39(3):691-697.
  42. Fisichella PM, Davis CS, Lowery E, et al. Pulmonary immune changes early after laparoscopic antireflux surgery in lung transplant patients with gastroesophageal reflux disease. J Surg Res. 2012;177(2):e65-e73.
  43. Van Raemdonck D. Thoracic organs: Current preservation technology and future prospects; part 1: Lung. Curr Opin Organ Transplant. 2010;15(2):150-155.
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  45. Cypel M, Waddell T, Keshavjee S. Lung transplantation: Donor lung preservation. Last reviewed January 2013. UpToDate Inc. Waltham, MA.


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