Should cytomegalovirus be tested for in both blood and bronchoalveolar lavage fluid of patients at a high risk of CMV pneumonia after bone marrow transplantation?
Autor: | Salord Jm, Terrier P, E Gautier, Cyrille Tancrede, A. Ibrahim, Roittmann S, Fajac A, Bernaudin Jf, Charnoz I, J. H. Bourhis, Jose-Luis Pico, M. Hayat |
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Rok vydání: | 1997 |
Předmět: |
Ganciclovir
Human cytomegalovirus Foscarnet Male Lymphoma Pneumonia Viral Cytomegalovirus Opportunistic Infections Betaherpesvirinae Risk Factors medicine Humans Viremia Bone Marrow Transplantation Leukemia medicine.diagnostic_test biology business.industry Respiratory disease virus diseases Hematology medicine.disease biology.organism_classification respiratory tract diseases Pneumonia surgical procedures operative Bronchoalveolar lavage medicine.anatomical_structure Immunology Cytomegalovirus Infections Female Bone marrow business Bronchoalveolar Lavage Fluid medicine.drug |
Zdroj: | British journal of haematology. 98(1) |
ISSN: | 0007-1048 |
Popis: | To identify and treat patients at high risk of cytomegalovirus (CMV) pneumonia after bone marrow transplantation (BMT), we tested for CMV viraemia weekly, and performed broncho-alveolar lavage (BAL) on day 35 post-transplant in 63 recipients. 36 allogeneic BMT recipients were at a high risk of CMV pneumonia (25 CMV-seropositive recipients and 11 patients receiving marrow from a CMV-seropositive donor). Patients with a positive BAL or viraemia received a 14 d course of ganciclovir or foscarnet. CMV was detected in 29 (46%) of the 63 BMT recipients and excretion of CMV in blood and BAL was significantly linked. However, among the 29 patients who excreted the virus, only 10 (35%) shed CMV in blood and BAL at the same time: 19 patients (65%) had detectable CMV in blood (11 patients) or BAL (eight patients) only. Therefore, on the basis of viraemia or BAL alone, 21/29 patients (70%) and 18/29 patients (60%), respectively, would have received antiviral treatment. BAL increased the CMV detection rate by 13% (8/63 patients) relative to viraemia. With this strategy, the incidence of CMV pneumonia was reduced to 3% in allografted patients. Only two of the 19 autografted patients developed fatal CMV pneumonia. We avoided anti-CMV treatment in 54% of all the BMT recipients. In conclusion, CMV should be tested for in both blood and BAL fluid of BMT recipients at high risk of CMV pneumonia. |
Databáze: | OpenAIRE |
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