2020
DOI: 10.1111/jvh.13308
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Response to direct‐acting antivirals for hepatitis C treatment in vertically HIV/HCV co‐infected patients

Abstract: Direct‐acting antivirals (DAAs) for HCV treatment have improved tolerance and efficacy among adults, but experience in vertical transmission is scarce. In our vertically HIV/HCV co‐infected youth cohort of 58 patients, DAA achieved excellent rates of cure among naïve and pretreated individuals. Treating vertically infected seems important as 29.6% displayed advanced fibrosis at treatment initiation.

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Cited by 9 publications
(13 citation statements)
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“…To date, direct acting antivirals (DAAs) have been approved for the treatment of all HCV-infected children aged 12 to 17 years. DAAs are a safe and effective option in perinatally infected HIV/HCV patients; therapy should be started early to prevent disease progression [ 91 , 92 ].…”
Section: Hepatopancreatic Disordersmentioning
confidence: 99%
“…To date, direct acting antivirals (DAAs) have been approved for the treatment of all HCV-infected children aged 12 to 17 years. DAAs are a safe and effective option in perinatally infected HIV/HCV patients; therapy should be started early to prevent disease progression [ 91 , 92 ].…”
Section: Hepatopancreatic Disordersmentioning
confidence: 99%
“…The FDA has cleared this combination of monoclonal antibodies to SARS-COV-2 on an emergency basis (REGEN-COV) for co-administration by intravenous or subcutaneous injection for the treatment of mild to moderate COVID-19 in individuals over 12 years of age and weighing no less than 40 kg who are at high risk for progression to severe COVID-19 [61,62]. Traditional risk groups would also include overweight patients or pregnant women, as well as those suffering from cardiovascular disease, hypertension or chronic respiratory disease (Table 1) [61,63,64].…”
Section: Casirivimab + Imdevimabmentioning
confidence: 99%
“…FDA clearance was based on interim Phase 1/2 results from a double-blind trial (COV-2067) in which 799 outpatients with mild to moderate COVID-19 were randomized in a blinded fashion to receive a single intravenous infusion of monoclonals or placebo. Outcomes were assessed 28 days after infusion [64] and viral load at day 7 was significantly lower with the monoclonal combination than with placebo. There was also less need for hospitalization, emergency department visit or teleconsultation within 28 days after infusion (2.8% vs. 6.5%).…”
Section: Combination Of Neutralizing Monoclonal Antibodies Brii-196 A...mentioning
confidence: 99%
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“…A 12-wk course with sofosbuvir/ledipasvir was found to allow autologous HSC-GT for the correction of severe combined immunodeficiency caused by adenosine deaminase deficiency as described in a pioneering study[ 59 ]. Pediatric studies have not yet replicated the encouraging results with DAA in adults with HIV/HCV coinfection[ 60 - 62 ], even when vertically transmitted[ 63 ], nor for the treatment of HCV in hemodialyzed[ 64 ] and kidney transplant patients[ 65 , 66 ].…”
Section: Hcv Treatment Of Hcv In Children At Riskmentioning
confidence: 99%