Table 1.
Statistics on the epidemiology of HSK.
Statistics | Prevalence and percentages | References |
---|---|---|
Prevalence of HSK in US | 150 in 100,000, and 20K new cases annually | (Liesegang et al. 1989) |
Annual incidence in western countries | 10–30 per 100,000 | (Labetoulle et al. 2005, Liesegang et al. 1989, Young et al. 2010) |
% of people with antibodies to HSV-1 by middle age | More than 90% | (Liesegang. 2001b) |
% of primary HSV-1 infections that are asymptomatic and not recognized | More than 90% | (Liesegang. 2001b) |
% Recurrence at 1 yr, 2 yrs, 5 yrs, and 10 yrs | 9.6%, 22.9%, 40.0%, 67.0% | (Farooq and Shukla. 2012, Labetoulle et al. 2005, Liesegang. 2001b, Shuster et al. 1981, Stanzel et al. 2014) |
Global lifetime risk of developing HSK | 1% | (Reynaud et al. 2017) |
Patients who experience 2–5 relapses of HSK over their lifetime vs 6–15 relapses | 40% vs 11% | (Wishart et al. 1987) |
% of patients with HSK who develop severe complications | 15% | (Darougar et al. 1985) |
Incidence of ACV-resistant strains among immunocompetent patients | 0–0.6% | (Christophers et al. 1998, Nugier et al. 1992) |
Incidence of ACV-resistant strains among immunocompromised patients | 3–6% with 14% for bone marrow transplant recipients | (Christophers et al. 1998, Nugier et al. 1992) |