2019
DOI: 10.1080/21645515.2019.1621148
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The indications and safety of polyvalent immunoglobulin for post-exposure prophylaxis of hepatitis A, rubella and measles

Abstract: Derived from pooled blood donations, polyvalent immunoglobulins are used for post-exposure prophylaxis as one aspect of the public health management of hepatitis A, rubella and measles. This review summarizes the safety profile of these blood products and the current recommendations for their use for the prevention of hepatitis A, rubella and measles among people who have been exposed to these diseases. The current recommendations are drawn from the most recent publicly available national guidelines of the Uni… Show more

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Cited by 18 publications
(14 citation statements)
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“…And according to the dose of different, in different time has a protective effect. [24] Active immunization: Vaccines. The approval and widespread use of the 1990s HAV vaccine has paved the way for the prevention of this disease.…”
Section: Discussionmentioning
confidence: 99%
“…And according to the dose of different, in different time has a protective effect. [24] Active immunization: Vaccines. The approval and widespread use of the 1990s HAV vaccine has paved the way for the prevention of this disease.…”
Section: Discussionmentioning
confidence: 99%
“…195,196 Hyperimmune globulin is currently used for post-exposure prophylaxis in the treatment of several viral infections, including hepatitis B (HBV), rabies, tetanus toxin, varicella-zoster, rubella, measles, etc. 30,[197][198][199] The COVID-19 pandemic attracted much new research to develop therapeutic drug options, [200][201][202][203] including CPT 80,88,93,102,113,204 to treat patients as no specific medication is available. Initially, the US FDA approved and served EUA, 80,205 regarding CPT but later amended the earlier policy (September-2-2020).…”
Section: Discussionmentioning
confidence: 99%
“…Однако для производства и сертификации нового специфического иммуноглобулина, как и для производства новой вакцины, требуется достаточно длительное время. Крупнейшие мировые производители плазмы объединили свои усилия в CoVIg-9 Plasma Allianse для скорейшего получения и апробации такого гипериммунного иммуноглобулинового препарата, который позволил бы сделать терапию антителами против SARS-CoV-2 более стандартизированной и простой, но пока на фармацевтическом рынке его нет и неизвестно, когда он может появиться [35,36]. Для инициализации фракционирования и производства иммуноглобулина в России запас РП с высоким содержанием ВНА-антител должен быть значительным.…”
Section: Discussionunclassified