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Outcomes of Intravenous Immunoglobulin treatment of immunocompromised patients with viral respiratory infections.
Moughames, Eric; Sakayan, Sevag; Prichett, Laura; Runken, M Chris; Borst, Dawn; Tversky, Jody; Azar, Antoine.
Affiliation
  • Moughames E; Department of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland. Electronic address: emougha2@jhmi.edu.
  • Sakayan S; Ain Shams University, Faculty of Medicine, Cairo, Egypt.
  • Prichett L; Biostatistics, Epidemiology, and Data Management (BEAD) Core, Department of Pediatrics, Johns Hopkins School of Medicine, Baltimore, Maryland.
  • Runken MC; Grifols SSNA, Research Triangle Park, NC.
  • Borst D; Department of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
  • Tversky J; Department of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
  • Azar A; Department of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Article in En | MEDLINE | ID: mdl-39251021
ABSTRACT

BACKGROUND:

Limited guidelines exist for treating immunocompromised patients hospitalized for acute viral respiratory infection. Little is known about clinical and economic benefits of IVIG administration in patients with acute viral respiratory infections.

OBJECTIVE:

We compared clinical and economic outcomes among immunocompromised patients hospitalized with viral respiratory infections who received IVIG to those who did not.

METHODS:

We performed a retrospective cohort study on all patients hospitalized for a respiratory viral infection between 2011 and 2016 at two large academic centers including data on age, gender, virus species, immunosuppression type, and receipt of IVIG. Outcomes included death, hospital readmission, length of stay (LOS) in the hospital, and the intensive care unit (ICU).

RESULTS:

A total of 270 patient admissions were reviewed, and 35.6% received IVIG. The average age was 40.6 years, 50% were female and 74% were transplant patients. The most common virus was rhinovirus (50.7%). Use of IVIG was significantly associated with a shorter ICU LOS (ß=-0.534, P=0.012), and a longer hospital LOS (ß=0.887, P<0.01). IVIG administered within 48 hours of hospitalization (n=229) was associated with a shorter ICU LOS (ß=-2.08, P=0.001) and a shorter hospital LOS for patients hospitalized at least 2 days (ß=-0.461, P=0.007). There were no significant differences in readmission rates or death.

CONCLUSION:

This double-center, retrospective cohort analysis is one of the first studies to evaluate the effect of IVIG on immunocompromised patients hospitalized with respiratory viral infections. IVIG was associated with a shorter hospital and ICU LOS, especially when administered within 48 hours of admission.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ann Allergy Asthma Immunol Journal subject: ALERGIA E IMUNOLOGIA Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ann Allergy Asthma Immunol Journal subject: ALERGIA E IMUNOLOGIA Year: 2024 Document type: Article Country of publication: United States