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1.
Bone Marrow Transplant ; 45(5): 945-50, 2010 May.
Article in English | MEDLINE | ID: mdl-19784077

ABSTRACT

Patients who undergo allogeneic hematopoietic SCT (HSCT) are prone to pulmonary infections. Between 1998 and 2004, a total of 450 patients underwent HSCT at Karolinska University Hospital, Huddinge. Pneumonia was diagnosed in 167 patients (37%), including 42 children. Bronchoalveolar lavage (BAL) was performed on 68 occasions in 57 patients (six children). In 110 patients (36 children) with pneumonia, BAL was not performed. BAL contributed to the diagnosis in 43 cases (63%) and to relevant findings in 53 cases: bacteria (n=13, 24%), viruses (n=28, 53%) and fungi (n=12, 23%). In 25 cases BAL was negative. In 15 of these cases, BAL was performed >or=4 days after chest X-ray, and in four cases not in the same segment as the infiltrations. The median time between radiographic findings and positive BAL was 2 (0-15) days, and a negative BAL 6 (1-30) days (P<0.001). Antimicrobial treatment was administered to 79% patients with positive findings, and to 92% with negative findings at the time of BAL. No serious complications due to the procedure were reported. BAL resulted in a changed treatment in 32/68 (47%) episodes of pneumonia. To conclude, BAL is a safe and useful diagnostic procedure that should be performed early after the onset of pneumonia following allogeneic HSCT.


Subject(s)
Bronchoalveolar Lavage/methods , Graft vs Host Disease/prevention & control , Pneumonia/therapy , Adolescent , Adult , Aged , Child , Child, Preschool , Female , Graft vs Host Disease/diagnosis , Graft vs Host Disease/therapy , Hematopoietic Stem Cell Transplantation , Humans , Infant , Infant, Newborn , Male , Middle Aged , Pneumonia/diagnosis , Tissue Donors , Transplantation, Homologous , Young Adult
2.
Acta Paediatr ; 92(8): 910-5, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12948065

ABSTRACT

AIM: To evaluate the response rate to antimycobacterial drug therapy in patients with cystic fibrosis (CF) suffering from infection by non-tuberculous mycobacteria (NTM). METHODS: Ten patients, aged 10-34 y, out of 180 CF patients, were diagnosed with NTM disease. They had been regularly checked and examined for pulmonary symptoms, and had had chest X-rays and sputum cultures (including for mycobacteria) performed. One additional 36-y-old female received her CF diagnosis soon after the NTM diagnosis. RESULTS: Mycobacterium avium-intracellulare complex (MAC) was found in 10 out of 11 patients and M. kansasii in 1 patient. Treatment with antimycobacterial drugs resulted in clinical improvement (weight gain or stabilization of weight and/or improved or stabilized lung function in 8 out of 11 patients) and mycobacterial culture turned negative in 10 out of 1. CONCLUSION: Promising results may be associated with early intervention with antimycobacterial therapy in CF patients.


Subject(s)
Antitubercular Agents/therapeutic use , Cystic Fibrosis/complications , Ethambutol/therapeutic use , Mycobacterium Infections, Nontuberculous/complications , Mycobacterium Infections, Nontuberculous/drug therapy , Adolescent , Adult , Amikacin/therapeutic use , Anti-Bacterial Agents/adverse effects , Anti-Bacterial Agents/therapeutic use , Antitubercular Agents/adverse effects , Child , Clarithromycin/therapeutic use , Cohort Studies , Cystic Fibrosis/drug therapy , Ethambutol/adverse effects , Female , Humans , Male , Mycobacterium avium Complex/isolation & purification , Mycobacterium avium-intracellulare Infection/complications , Mycobacterium avium-intracellulare Infection/drug therapy , Mycobacterium kansasii/isolation & purification , Retrospective Studies , Rifampin/adverse effects , Rifampin/therapeutic use , Streptomycin/therapeutic use
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