Graft Loss and CLAD-Onset Is Hastened by Viral Pneumonia After Lung Transplantation. Issue 11 (November 2016)
- Record Type:
- Journal Article
- Title:
- Graft Loss and CLAD-Onset Is Hastened by Viral Pneumonia After Lung Transplantation. Issue 11 (November 2016)
- Main Title:
- Graft Loss and CLAD-Onset Is Hastened by Viral Pneumonia After Lung Transplantation
- Authors:
- Allyn, Paul R.
Duffy, Erin L.
Humphries, Romney M.
Injean, Patil
Weigt, S. Samuel
Saggar, Rajan
Shino, Michael Y.
Lynch, Joseph P.
Ardehali, Abbas
Kubak, Bernard
Tseng, Chi-Hong
Belperio, John A.
Ross, David J.
Gregson, Aric L. - Abstract:
- Abstract : Background: Community-acquired respiratory virus (CARV) infections occur frequently after lung transplantation and may adversely impact outcomes. We hypothesized that while asymptomatic carriage would not increase the risk of chronic lung allograft dysfunction (CLAD) and graft loss, severe infection would. Methods: All lung transplant cases between January 2000 and July 2013 performed at our center were reviewed for respiratory viral samples. Each isolation of virus was classified according to clinical level of severity: asymptomatic, symptomatic without pneumonia, and viral pneumonia. Multivariate Cox modeling was used to assess the impact of CARV isolation on progression to CLAD and graft loss. Results: Four thousand four hundred eight specimens were collected from 563 total patients, with 139 patients producing 324 virus-positive specimens in 245 episodes of CARV infection. Overall, the risk of CLAD was elevated by viral infection (hazard ratio [HR], 1.64; P < 0.01). This risk, however, was due to viral pneumonia alone (HR, 3.94; P < 0.01), without significant impact from symptomatic viral infection (HR, 0.97; P = 0.94) nor from asymptomatic viral infection (HR, 0.99; P = 0.98). The risk of graft loss was not increased by asymptomatic CARV infection (HR, 0.74; P = 0.37) nor symptomatic CARV infection (HR, 1.39; P = 0.41). Viral pneumonia did, however, significantly increase the risk of graft loss (HR, 2.78; P < 0.01). Conclusions: With respect to CARV, onlyAbstract : Background: Community-acquired respiratory virus (CARV) infections occur frequently after lung transplantation and may adversely impact outcomes. We hypothesized that while asymptomatic carriage would not increase the risk of chronic lung allograft dysfunction (CLAD) and graft loss, severe infection would. Methods: All lung transplant cases between January 2000 and July 2013 performed at our center were reviewed for respiratory viral samples. Each isolation of virus was classified according to clinical level of severity: asymptomatic, symptomatic without pneumonia, and viral pneumonia. Multivariate Cox modeling was used to assess the impact of CARV isolation on progression to CLAD and graft loss. Results: Four thousand four hundred eight specimens were collected from 563 total patients, with 139 patients producing 324 virus-positive specimens in 245 episodes of CARV infection. Overall, the risk of CLAD was elevated by viral infection (hazard ratio [HR], 1.64; P < 0.01). This risk, however, was due to viral pneumonia alone (HR, 3.94; P < 0.01), without significant impact from symptomatic viral infection (HR, 0.97; P = 0.94) nor from asymptomatic viral infection (HR, 0.99; P = 0.98). The risk of graft loss was not increased by asymptomatic CARV infection (HR, 0.74; P = 0.37) nor symptomatic CARV infection (HR, 1.39; P = 0.41). Viral pneumonia did, however, significantly increase the risk of graft loss (HR, 2.78; P < 0.01). Conclusions: With respect to CARV, only viral pneumonia increased the risk of both CLAD and graft loss after lung transplantation. In the absence of pneumonia, respiratory viruses had no impact on measured outcomes. Abstract : Community-acquired viral pneumonia, especially from adenovirus, parainfluenza virus, and Coxsackie/echovirus, but not influenza and respiratory syncytial virus, increases the risk for chronic lung allograft dysfunction and graft loss. But, asymptomatic viral infection or even symptomatic viral infection without pneumonia do not. … (more)
- Is Part Of:
- Transplantation. Volume 100:Issue 11(2016)
- Journal:
- Transplantation
- Issue:
- Volume 100:Issue 11(2016)
- Issue Display:
- Volume 100, Issue 11 (2016)
- Year:
- 2016
- Volume:
- 100
- Issue:
- 11
- Issue Sort Value:
- 2016-0100-0011-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-11
- Subjects:
- Transplantation of organs, tissues, etc -- Periodicals
Transplantation immunology -- Periodicals
617.95 - Journal URLs:
- http://journals.lww.com/pages/default.aspx ↗
- DOI:
- 10.1097/TP.0000000000001346 ↗
- Languages:
- English
- ISSNs:
- 0041-1337
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9024.990000
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