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HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 1107A<br />

of increasing the number of PWIDs treated with new oral DAAs<br />

was considered, including the annual number needed to treat<br />

in order to reduce the HCV-infected PWID population by 2030.<br />

Results: If the current transmission paradigm continues, there<br />

are projected to be 3,620 HCV infected PWIDs in 2030.<br />

Annually treating 40 HCV-infected PWIDs with new oral DAAs<br />

(1% of HCV-infected PWID population in 2014) resulted in a<br />

5% reduction in HCV-infected PWIDs by 2030, while annual<br />

treatment of 200 PWIDs (5% of 2014 population) resulted in a<br />

reduction of over 25% by 2030. Treating 387 PWIDs annually<br />

(17% of 2014 population) resulted in a >90% reduction in<br />

HCV-infected PWIDs by 2030. Targeting treatment to PWIDs<br />

engaged in OST and NEP would provide the greatest reduction<br />

in prevalence for the number of individuals treated (2.2 treated<br />

in OST/NEP to reduce prevalence by 1, as compared with 6.8<br />

treated in the general population). Conclusions: The results<br />

show that treating yet a small amount of PWIDs resulted in<br />

substantial decreases in the HCV infected PWID population by<br />

2030. Furthermore, the relative impact of treatment was greatest<br />

when focused on the population engaged in OST and NEP.<br />

Treatment is expected to increase the rate of reinfection; however,<br />

reinfection will decline as HCV prevalence decreases.<br />

This analysis supports the implementation of a screening and<br />

treatment strategy among PWIDs when combined with an<br />

expansion of harm reduction programs.<br />

Disclosures:<br />

Stefan Bourgeois - Advisory Committees or Review Panels: AbbVIe, Gilead; Consulting:<br />

Roche, MSD; Speaking and Teaching: Janssen, BMS<br />

Sarah Blach - Employment: Center for Disease Analysis<br />

Homie Razavi - Management Position: Center for Disease Analysis<br />

Geert Robaeys - Advisory Committees or Review Panels: Gilead; Speaking and<br />

Teaching: Merck, Janssens<br />

The following authors have nothing to disclose: Catharina Mathei, Christian<br />

Brixko, Jean-Pierre Mulkay, Thomas Sersté<br />

1843<br />

Non-Invasive Fibrosis Scores: Do They Predict Antiviral<br />

Treatment Response, Decompensation, Hepatocellular<br />

Carcinoma and Significant Liver Related Adverse Events<br />

in Chronic Hepatitis C?<br />

Ragesh B. Thandassery 1 , Madiha E. Soofi 1 , Anil John 1 , Samir S.<br />

Nairat 1 , Abdulrahman A. Alfadda 2 , Saad R. Al Kaabi 1 ; 1 Hamad<br />

Medical Corporation, Doha, Qatar; 2 King Faisal Specialist Hospital<br />

and Research Center, Riyadh, Saudi Arabia<br />

Background The role of non-invasive liver fibrosis scores (NIF)<br />

in predicting antiviral treatment (AVT) response and post treatment<br />

significant liver related events (SLRE) in chronic hepatitis<br />

C (CHC) is less studied. Aim To compare 12 simple NIF,<br />

derived from routine blood investigations, for predicting<br />

response to AVT and SLRE. Methods 1605 patients underwent<br />

liver biopsy (LB, Scheuer classification) and received AVT<br />

(pegylated interferon and ribavirin). 12 NIF [AST-platelet count<br />

ratio index (APRI), Fibrosis-4 (FIB-4) score, Lok score, GUCI<br />

score, Fibroalpha score, modified APRI, King score, AST-ALT<br />

ratio (AAR), Fibrosis Index (FI), Fibro score, Fibrosis cirrhosis<br />

index (FCI) and Globulin platelet index (GPI)] were calculated<br />

prior to AVT. AUROCs were calculated for each of these NIF<br />

for predicting non-response to AVT and development of SLRE<br />

(defined as development of any event requiring intervention;<br />

decompensation and hepatocellular carcinoma, HCC) on<br />

follow-up Results Mean age 41.9years, predominantly genotype<br />

4(65%).1089(67.8%) were responders, 482(30%) non<br />

responders and 34(2.1%) relapsers. After median follow-up of<br />

6580.5 patient-years; 52(3.2%) had decompensation (bleed-<br />

9, ascites-39, jaundice-22, hepatic encephalopathy-7, spontaneous<br />

bacterial peritonitis-10, hepatorenal syndrome-4),<br />

11(0.7%) had HCC and 60(3.7%) had SLRE. The predictive<br />

accuracy of NIF and LB for non-response to AVT was low.<br />

FibroQ, King score and FIB-4 showed high accuracy for predicting<br />

adverse events. For predicting decompensation, HCC<br />

and SLRE, FibroQ (0.88), King score (0.90) and FibroQ (0.87)<br />

had highest AUROC respectively. Conclusions Predictive accuracy<br />

of NIF for non-response to treatment was low. Some NIF<br />

have high accuracy for predicting development of decompensation,<br />

HCC and SLRE on follow-up. Application of these simple<br />

scores can improve assessment of liver prognosis in patients<br />

treated for CHC.<br />

Non-invasive scores in predicting post treatment events<br />

* AUROC(95% Confidence interval)<br />

Disclosures:<br />

The following authors have nothing to disclose: Ragesh B. Thandassery, Madiha<br />

E. Soofi, Anil John, Samir S. Nairat, Abdulrahman A. Alfadda, Saad R. Al Kaabi

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