Review of the Safety, Efficacy and Tolerability of Palivizumab in the Prevention of Severe Respiratory Syncytial Virus (RSV) Disease.

IF 2.2 Q2 HEALTH CARE SCIENCES & SERVICES Drug, Healthcare and Patient Safety Pub Date : 2023-09-11 eCollection Date: 2023-01-01 DOI:10.2147/DHPS.S348727
Shaun O'Hagan, Niamh Galway, Michael D Shields, Peter Mallett, Helen E Groves
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Abstract

Respiratory Syncytial Virus (RSV) is a major global cause of childhood morbidity and mortality. Palivizumab, a monoclonal antibody that provides passive immunity against RSV, is currently licensed for prophylactic use in specific "high-risk" populations, including congenital heart disease, bronchopulmonary dysplasia and prematurity. Available research suggests palivizumab use in these high-risk populations can lead to a reduction in RSV-related hospitalization. However, palivizumab has not been demonstrated to reduce mortality, adverse events or length of hospital stay related to RSV. In this article, we review the management of RSV, indications for palivizumab prophylaxis, the safety, cost-effectiveness and efficacy of this preventative medication, and emerging therapeutics that could revolutionize future prevention of this significant pathogen.

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帕利单抗预防严重呼吸道合胞病毒(RSV)疾病的安全性、有效性和耐受性综述。
呼吸道合胞病毒(RSV)是全球儿童发病率和死亡率的主要原因。帕利单抗是一种提供对呼吸道合胞病毒被动免疫的单克隆抗体,目前已获准在特定的“高危”人群中预防性使用,包括先天性心脏病、支气管肺发育不良和早产。现有研究表明,在这些高危人群中使用帕利单抗可以减少呼吸道合胞病毒相关的住院治疗。然而,帕利单抗尚未被证明可以降低与呼吸道合胞病毒相关的死亡率、不良事件或住院时间。在这篇文章中,我们回顾了呼吸道合胞病毒的管理、帕利单抗预防的适应症、这种预防性药物的安全性、成本效益和疗效,以及可能在未来彻底预防这种重要病原体的新兴疗法。
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来源期刊
Drug, Healthcare and Patient Safety
Drug, Healthcare and Patient Safety HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.10
自引率
0.00%
发文量
24
审稿时长
16 weeks
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