Burden of human metapneumovirus infections in patients with cancer: Risk factors and outcomes

  • Firas El Chaer
  • , Dimpy P. Shah
  • , Joumana Kmeid
  • , Ella J. Ariza-Heredia
  • , Chitra M. Hosing
  • , Victor E. Mulanovich
  • , Roy F. Chemaly

Producción científica: Articlerevisión exhaustiva

34 Citas (Scopus)

Resumen

BACKGROUND: Human metapneumovirus (hMPV) causes upper and lower respiratory tract infections (URIs and LRIs, respectively) in healthy and immunocompromised patients; however, its clinical burden in patients with cancer remains unknown. METHODS: In a retrospective study of all laboratory-confirmed hMPV infections treated at the authors’ institution between April 2012 and May 2015, clinical characteristics, risk factors for progression to an LRI, treatment, and outcomes in patients with cancer were determined. RESULTS: In total, 181 hMPV infections were identified in 90 patients (50%) with hematologic malignancies (HMs), in 57 (31%) hematopoietic cell transplantation (HCT) recipients, and in 34 patients (19%) with solid tumors. Most patients (92%) had a community-acquired infection and presented with URIs (67%), and 43% developed LRIs (59 presented with LRIs and 19 progressed from a URI to an LRI). On multivariable analysis, an underlying HM (adjusted odds ratio [aOR], 3.11; 95% confidence interval [CI], 1.12-8.64; P =.029), nosocomial infection (aOR, 26.9; 95% CI, 2.79-259.75; P =.004), and hypoxia (oxygen saturation [SpO2], ≤ 92%) at presentation (aOR, 9.61; 95% CI, 1.98-46.57; P =.005) were identified as independent factors associated with LRI. All-cause mortality at 30 days from hMPV diagnosis was low (4%), and patients with LRIs had a 10% mortality rate at day 30 from diagnosis; whereas patients with URIs had a 0% mortality rate. CONCLUSIONS: hMPV infections in patients with cancer may cause significant morbidity, especially for those with underlying HM who may develop an LRI. Despite high morbidity and the lack of directed antiviral therapy for hMPV infections, mortality at day 30 from this infection remained low in this studied population. Cancer 2017;123:2329–2337.

Idioma originalEnglish (US)
Páginas (desde-hasta)2329-2337
Número de páginas9
PublicaciónCancer
Volumen123
N.º12
DOI
EstadoPublished - jun 15 2017
Publicado de forma externa

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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