294 Good Outcome of RSV Infection without Ribavirin Treatment in Pediatric Bone Marrow Transplantation

Track: Poster Abstracts
Wednesday, February 11, 2015, 6:45 PM-7:45 PM
Grand Hall CD (Manchester Grand Hyatt)
Javier El-Bietar, MD , Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH
Adam Stuart Nelson, MD , Cincinnati Children's Hospital Medical Center, Cincinnati, OH
Gregory Wallace, DO , Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH
Christopher E Dandoy, MD, MSc , Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH
Sonata Jodele, MD , Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH
Kasiani C. Myers, MD , Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH
Stella M. Davies, MBBS, PhD, MRCP , Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH
Lara Danziger-Isakov, MD, MPH , Infectious Disease, Cincinnati Children's Hospital Medical Center, Cincinnati, OH
Presentation recording not available for download or distribution as requested by the presenting author.
Clinicians commonly use inhaled ribavirin to treat HSCT recipients with Respiratory Syncytial Virus (RSV); however, limited data exist to support this therapy. We evaluated 349 consecutive patients transplanted between June, 2008 and December, 2013.  Eighteen (5.2%) pediatric and young adult patients (6 months to 25 years of age) developed an RSV infection. Fifteen (83%) patients presented with an upper respiratory tract infection (URTI) identified a median of 151 (range 3 – 621) days post-HSCT and 3 (17%) presented with, or progressed to, a lower respiratory tract infection (LRTI) identified a median of 33 (range 10 – 117) days post-HSCT.  All 3 patients with LRTI had significant co-infections while 2/3 were less than 1 year of age at the time RSV was identified.  Fifteen (83%, 13/15 with URTI and 2/3 with LRTI) were still receiving immunosuppressants.  All 18 patients were lymphopenic (median 280, range 0 – 2120).   Eleven of 15 (73%) patients with URTI and all 3 patients with LRTI were receiving routine intravenous immunoglobulin (IVIG) supplementation every 1-2 weeks to maintain normal IGG levels after HSCT. RSV-targeted treatment included an increase in frequency or additional IVIG administration for 4/15 and 3/3 URTI and LRTI patients, respectively.  Three URTI patients and 2 LRTI patients receiving IVIG were also given palivizumab. No patients received inhaled ribavirin or died as a direct result of RSV infection suggesting that ribavirin may not be an essential component of RSV treatment in pediatric HSCT recipients.
Disclosures:
Nothing To Disclose