scholarly journals Effects of Antiviral Therapy and Glucocorticoid Therapy on Fever Duration in Pediatric Patients with Influenza

Medicina ◽  
2021 ◽  
Vol 57 (12) ◽  
pp. 1385
Author(s):  
Ji Yoon Han ◽  
Eun Ae Yang ◽  
Jung-Woo Rhim ◽  
Seung Beom Han

Background and Objectives: Considering developing resistance against neuraminidase inhibitors (NAIs) and their adverse reactions, restricted use of NAIs and use of alternative drugs should be considered for treating influenza. Although glucocorticoids (GCs) have been used for severe influenza, their effects on non-severe influenza have rarely been evaluated. This study aimed to evaluate the clinical responses to NAI therapy and GC therapy in pediatric patients with non-severe influenza. Materials and Methods: A total of 601 pediatric patients (<19 years of age) diagnosed with non-severe influenza were retrospectively recruited to evaluate the effects of NAI therapy and GC therapy. Post-admission fever duration and hospitalization duration were compared among four patient groups divided by the administered treatment: No therapy (n = 52), NAI therapy (n = 154), GC therapy (n = 123), and Both therapies (n = 272). Results: In a multivariate analysis with adjustment for confounding variables, the post-admission fever duration was not significantly different among the four patient groups. The post-admission fever duration tended to shorten with increasing age, longer pre-admission fever duration, and incidence of influenza A virus infection and lower respiratory tract infection. The type of administered treatment showed no significant effects on the post-admission fever duration in any subgroups according to patient age, pre-admission fever duration, influenza virus subtype, and clinical diagnosis. Conclusions: Symptomatic treatment rather than antiviral or GC therapy seems to be sufficient for patients with non-severe influenza, although the effects of NAI therapy and GC therapy according to their administered time and dose should be further evaluated.

2020 ◽  
Vol 15 (7) ◽  
pp. 441-453
Author(s):  
Ana Vazquez-Pagan ◽  
Rebekah Honce ◽  
Stacey Schultz-Cherry

Pregnant women are among the individuals at the highest risk for severe influenza virus infection. Infection of the mother during pregnancy increases the probability of adverse fetal outcomes such as small for gestational age, preterm birth and fetal death. Animal models of syngeneic and allogeneic mating can recapitulate the increased disease severity observed in pregnant women and are used to define the mechanism(s) of that increased severity. This review focuses on influenza A virus pathogenesis, the unique immunological landscape during pregnancy, the impact of maternal influenza virus infection on the fetus and the immune responses at the maternal–fetal interface. Finally, we summarize the importance of immunization and antiviral treatment in this population and highlight issues that warrant further investigation.


2021 ◽  
Vol 10 (10) ◽  
pp. 2056
Author(s):  
Frank Herbstreit ◽  
Marvin Overbeck ◽  
Marc Moritz Berger ◽  
Annabell Skarabis ◽  
Thorsten Brenner ◽  
...  

Infections with SARS-CoV-2 spread worldwide early in 2020. In previous winters, we had been treating patients with seasonal influenza. While creating a larger impact on the health care systems, comparisons regarding the intensive care unit (ICU) courses of both diseases are lacking. We compared patients with influenza and SARS-CoV-2 infections treated at a tertiary care facility offering treatment for acute respiratory distress syndrome (ARDS) and being a high-volume facility for extracorporeal membrane oxygenation (ECMO). Patients with COVID-19 during the first wave of the pandemic (n = 64) were compared to 64 patients with severe influenza from 2016 to 2020 at our ICU. All patients were treated using a standardized protocol. ECMO was used in cases of severe ARDS. Both groups had similar comorbidities. Time in ICU and mortality were not significantly different, yet mortality with ECMO was high amongst COVID-19 patients with approximately two-thirds not surviving. This is in contrast to a mortality of less than 40% in influenza patients with ECMO. Mortality was higher than estimated by SAPSII score on admission in both groups. Patients with COVID-19 were more likely to be male and non-smokers than those with influenza. The outcomes for patients with severe disease were similar. The study helps to understand similarities and differences between patients treated for severe influenza infections and COVID-19.


2018 ◽  
Vol 24 (3) ◽  
pp. 566-568
Author(s):  
Michael Payne ◽  
Danuta Skowronski ◽  
Suzana Sabaiduc ◽  
Linda Merrick ◽  
Christopher Lowe

2014 ◽  
Vol 20 (9) ◽  
Author(s):  
Zongqiu Chen ◽  
Hui Liu ◽  
Jianyun Lu ◽  
Lei Luo ◽  
Kuibiao Li ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Luca Hensen ◽  
Patricia T. Illing ◽  
E. Bridie Clemens ◽  
Thi H. O. Nguyen ◽  
Marios Koutsakos ◽  
...  

AbstractIndigenous people worldwide are at high risk of developing severe influenza disease. HLA-A*24:02 allele, highly prevalent in Indigenous populations, is associated with influenza-induced mortality, although the basis for this association is unclear. Here, we define CD8+ T-cell immune landscapes against influenza A (IAV) and B (IBV) viruses in HLA-A*24:02-expressing Indigenous and non-Indigenous individuals, human tissues, influenza-infected patients and HLA-A*24:02-transgenic mice. We identify immunodominant protective CD8+ T-cell epitopes, one towards IAV and six towards IBV, with A24/PB2550–558-specific CD8+ T cells being cross-reactive between IAV and IBV. Memory CD8+ T cells towards these specificities are present in blood (CD27+CD45RA− phenotype) and tissues (CD103+CD69+ phenotype) of healthy individuals, and effector CD27−CD45RA−PD-1+CD38+CD8+ T cells in IAV/IBV patients. Our data show influenza-specific CD8+ T-cell responses in Indigenous Australians, and advocate for T-cell-mediated vaccines that target and boost the breadth of IAV/IBV-specific CD8+ T cells to protect high-risk HLA-A*24:02-expressing Indigenous and non-Indigenous populations from severe influenza disease.


Author(s):  
Pınar YAZICI ÖZKAYA ◽  
Eşe Eda TURANLI ◽  
Hamdi METİN ◽  
Ayça Aydın UYSAL ◽  
Candan ÇİÇEK ◽  
...  

2021 ◽  
Author(s):  
Yaa-Hui Dong ◽  
Jo-Hsuan Wu ◽  
Jiun-Ling Wang ◽  
Ho-Min Chen ◽  
James L. Caffrey ◽  
...  

Abstract Purpose Angiotensin converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) may modulate ACE2 level and the risk of viral infections. However, studies of the risk of the severity of influenza associated with ACEIs or ARBs in the real-world settings were limited and the findings are conflicting. Methods This case-control study evaluated the risk of developing severe influenza disease associated with ACEIs and ARBs in hypertension patients hospitalized for influenza from a population-based Taiwanese database. Logistic regression models were conducted to estimate ORs and 95% CIs associated with ACEIs or ARBs within 30 days before hospitalization. Results We included 1,369 cases (severe influenza patients) and 4,107 matched controls (non-severe influenza patients). ORs for any use of ACEIs and ARBs were 1.15 (95% CI, 0.93–1.42) and 0.97 (0.84–1.12) versus nonuse. Similarly, no significant association was observed for monotherapy with ACEIs (1.47; 0.95–2.29) or ARBs (0·76; 0.53–1.10) versus nonuse. Combination therapy between calcium channel blockers (CCBs) and either ACEIs (1.57; 0.91–2.70) or ARBs (1.23; 0·93-1.62) were not significantly different from CCBs alone. Conclusions Our findings did not suggest an association between ACEIs and/or ARBs and the severity of influenza. Stable patients should maintain their anti-hypertensive regimens in the influenza epidemic era.


2011 ◽  
Vol 8 (2) ◽  
Author(s):  
Turgut Teke ◽  
Ümmiye Duran ◽  
Emin Maden ◽  
Kazım Gezginç ◽  
Mehmet D Yavşan ◽  
...  

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