Skip to main content
. Author manuscript; available in PMC: 2019 Jul 11.
Published in final edited form as: Sci Transl Med. 2018 Jul 11;10(449):eaao4496. doi: 10.1126/scitranslmed.aao4496

Table 1. Equation 1 parameters, values and sources.

Transmission probability was calculated based on Equation 1 (Eq. 1). The parameters VL, s, ρ, and q used in Eq. 1 are described together with values and their ranges. Sources are identified; either calculated in this study, taken from previously published data or estimated from experts familiar with practices employed by injecting drug users. IU, international units; HCV, hepatitis C virus; HDSS, high dead space syringe; LDSS, low dead space syringe; IQR, interquartile range (Q1-Q3).

Parameter Description [units] Value [Range] Scenario Source
n Number [#] of transferred HCV RNA IUs by contaminated syringe VL·ρ·s Calculated as described in text and in Fig. 1
VL Donor’s viral load in blood [RNA IU / mL] Variable
[0 to 6 log10 IU/mL]
Experimental Values input for testing
(Fig. 4 and Table 1)
Time-dependent: 3 primary acute-phase viral kinetic patterns Self-limiting, transient, chronic outcome (Figs. 5A, B and C) InC3 Study (1720)
Time-dependent: 3 reinfection viral kinetic patterns Self-limiting (Low and high titer) and chronic outcome (Figs. 5D, E and F)
s Donor blood as a fraction of the mixture with illicit drugs [%] 25% [5%−50%] Expert view
ρ HCV RNA carry-over 0.6%
[0.02 to 2.6%]
LDSS Estimated in the current study
(Fig. 2)
3.1%
[1.4 to 7.2%]
HDSS
0.12%
[0.003 to 0.8%]
LDSS + rinse
0.38%
[0.03 to 0.77%]
HDSS + rinse
q Ratio of infectious doses to HCV RNA IU 17% [IQR 7–33%] Table S2 based on published studies
(8, 9, 11, 21, 22)