scholarly journals Successful outcome of therapy of acute hepatitis C following sexual and parenteral exposure – report of two cases

2016 ◽  
Vol 3 ◽  
pp. 128-131
Author(s):  
Katarzyna Mazur-Melewska ◽  
Anna Mania ◽  
Pawel Kemnitz ◽  
Magdalena Figlerowicz ◽  
Wojciech Służewski
2002 ◽  
Vol 36 (11) ◽  
pp. 1715-1718 ◽  
Author(s):  
Ersan Özaslan ◽  
Rahmi Yılmaz ◽  
Halis Simsek ◽  
Gonca Tatar

OBJECTIVE: Due to their antiproliferative activity, the probable effects of interferons on a fetus are a concern. We report on a pregnant patient who developed acute hepatitis C during pregnancy and was treated with a short course of interferon alfa therapy with a successful outcome. CASE SUMMARY: A 26-year-old woman was diagnosed with acute hepatitis C at the 16th week of pregnancy. She received a total dose of 72 million units of interferon alfa-2b during a 2 1/2 month period. Although the therapy was discontinued due to adverse effects, a complete biochemical and virologic response was obtained. Premature labor occurred and healthy, but growth-restricted, twin infants were born transvaginally. At 18 months of age, they had normal development, with a negative hepatitis C serology. DISCUSSION: The rate of transmission of hepatitis C virus from mother to infant is within the range of 1–5%. Although acute hepatitis C during pregnancy is a very rare occurrence, the mother is at a great risk for chronic infection. There is scarce literature about the probable effects of interferon use during pregnancy due to a lack of controlled studies in this special population. A total of 8 infants, including ours, exposed to interferon alfa and/or ribavirin during pregnancy showed no congenital anomalies or malformations. CONCLUSIONS: Patients with chronic hepatitis whose therapy can be delayed should not be treated with interferon due to a lack of controlled studies. However, women exposed to interferon inadvertently during pregnancy may be encouraged to continue pregnancy. In patients with acute hepatitis C during pregnancy, the use of interferon therapy should be considered with close monitoring.


2001 ◽  
Vol 120 (5) ◽  
pp. A567-A567 ◽  
Author(s):  
E JAECKEL ◽  
M CORNBERG ◽  
T SANTANTONIO ◽  
J MAYER ◽  
H WEDEMEYER ◽  
...  

1992 ◽  
Vol 68 (06) ◽  
pp. 781-781 ◽  
Author(s):  
A Gerritzen ◽  
B Scholt ◽  
R Kaiser ◽  
K E Schneweis ◽  
H-H Brackmann ◽  
...  

Author(s):  
Tanvi Khera ◽  
Yanqin Du ◽  
Daniel Todt ◽  
Katja Deterding ◽  
Benedikt Strunz ◽  
...  

Abstract Background Treatment with direct acting antivirals (DAAs) in patients with chronic hepatitis C infection leads to partial restoration of soluble inflammatory mediators (SIMs). In contrast, we hypothesized that early DAA treatment of acute hepatitis C with DAAs may normalize most SIMs. Methods In this study, we made use of a unique cohort of acute symptomatic hepatitis C who cleared HCV with a 6-week course of ledipasvir/sofosbuvir. Plasma samples were used for proximity extension assay (PEA) measuring 92 proteins. Results Profound SIM alterations were observed in acute HCV patients, with marked upregulation of IL-6 and CXCL10 while certain mediators were down-regulated (e.g. MCP-4, IL-7). During treatment and follow-up, the majority of SIMs decreased but not all normalized (e.g. CDCP1, IL-18). Of note, SIMs that were down-regulated before DAA treatment remained suppressed while others that were initially unchanged, declined to lower values during treatment and follow-up (e.g.CD244). Conclusions Acute hepatitis C was associated with marked changes in the soluble inflammatory milieu as compared to both chronic hepatitis patients and healthy controls. Whereas early DAA treatment partly normalized this altered signature, long-lasting imprints of HCV remained. Thus, acute HCV-induced changes in the immune system may persist even after a short duration of viremia.


2005 ◽  
Vol 76 (4) ◽  
pp. 520-525 ◽  
Author(s):  
Maha M. El Gaafary ◽  
Claire Rekacewicz ◽  
Amira Gamal Abdel-Rahman ◽  
Mohamed Farouk Allam ◽  
Mostafa El Hosseiny ◽  
...  

1995 ◽  
Vol 108 (4) ◽  
pp. A1082 ◽  
Author(s):  
CJ Healey ◽  
J Watson ◽  
M. Durridge ◽  
N Snowdon ◽  
J Christie ◽  
...  

Hepatology ◽  
2002 ◽  
Vol 36 (4) ◽  
pp. 993-1000 ◽  
Author(s):  
Alberto Larghi ◽  
Massimo Zuin ◽  
Andrea Crosignani ◽  
Maria Lisa Ribero ◽  
Cristina Pipia ◽  
...  

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