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. Author manuscript; available in PMC: 2024 Nov 1.
Published in final edited form as: Clin Microbiol Infect. 2023 Jul 31;29(11):1450.e1–1450.e7. doi: 10.1016/j.cmi.2023.07.026

Table 2.

Characteristics of HHV-6 detection

Summary Pre-LTV
N=376
Post-LTV
N=362
Patients with at least one HHV-6 test 63/376 (16.8) 46/362 (12.7)
 Patients with at least one HHV-6 test in blood 51/376 (13.6) 40/362 (11.1)
 Patients with at least one HHV-6 test in CSF 24/376 (6.4) 15/362 (4.1)
 Number of tests per patient, median (range) 1 (1, 9) 1 (1, 16)
 Days to first test (blood and/or CSF), median (IQR)a 38 (18, 58) 26 (13, 42)
Patients with at least one positive HHV-6 test among tested a 10/63 (15.9) 10/46 (21.7)
 Patients with at least one positive HHV-6 test in blooda 8/51 (15.7) 10/40 (25)
 Patients with at least one positive HHV-6 test in CSFa 2/24 (8.3) 2/15 (13.3)
 Days to first positive HHV-6 test (any site), median (IQR)b 37 (18, 58) 26.5 (25, 34)
 Number of positive HHV-6 tests in blood, median (IQR)c 1 (1,1) 2 (1,4)
HHV-6 viral load; log10 copies/mL, median (IQR)
 Viral load in blood at first positiveb 3.00 (2.40, 4.10) 2.70 (2.40, 5.00)
 Peak viral load in bloodb 3.17 (2.51, 4.14) 4.03 (2.89, 5.00)
 Peak viral load in CSFd 2.62 (2.40, 2.84) 3.39 (3.18, 3.61)
Patients treated for HHV-6 e, f 6/376 (1.6) 4/362 (1.1)

Results are reported as number with percentage in parenthesis unless specified otherwise.

CSF: cerebrospinal fluid, HHV-6: human herpesvirus-6, IQR: interquartile range, LTV: letermovir

a

Among tested patients

b

Among patients with a positive test (any site)

c

Among patients with a positive test in blood

d

Among patients with a positive test in CSF

e

Indications for treatment: in the pre-LTV cohort: neurological symptoms (n=5) (proven HHV-6 encephalitis (n=2), possible HHV-6 encephalitis (n=3)), rash (n=1); in the post-LTV cohort: altered mental status (n=3) (proven HHV-6 encephalitis (n=2), possible HHV-6 encephalitis (n=1)), delayed engraftment (n=1).

f

Antiviral therapy: ganciclovir in 5 patients in the pre-LTV cohort and 2 in the post-LTV cohort; foscarnet in 1 patient in the pre-LTV cohort and 2 in the post-LTV cohort.