TY - JOUR
T1 - Immune reconstitution inflammatory syndrome associated with toxoplasmic encephalitis in hiv-infected patients
T2 - a multicenter cohort study
AU - van Bilsen, Ward P H
AU - van den Berg, Charlotte H S B
AU - Rijnders, Bart J A
AU - Brinkman, Kees
AU - Mulder, Jan W.
AU - Gelinck, Luc B S
AU - Hoepelman, Andy I M
AU - Wit, Ferdinand W N M
AU - van de Beek, Diederik
AU - Prins, Jan M.
PY - 2017/6
Y1 - 2017/6
N2 - OBJECTIVES:: To investigate the incidence and risk factors of immune reconstitution inflammatory syndrome (IRIS) associated with toxoplasmic encephalitis (TE) in patients starting cART. DESIGN:: A historical multicenter cohort study. METHODS:: We included all HIV-infected patients diagnosed with TE in six Dutch hospitals between 1996 and 2016. Diagnosis of TE-IRIS was made using predefined IRIS criteria. We distinguished paradoxical TE-IRIS (worsening of underlying treated infection) from unmasking TE-IRIS (unmasking of subclinical infection after start of cART). We compared CD4 count, plasma viral load and timing of cART initiation between patients with and without paradoxical TE-IRIS. RESULTS:: 211 TE cases were included. Among 143 cases at risk for paradoxical TE-IRIS, we identified five cases of paradoxical TE-IRIS (3.5%). In six other cases we could not differentiate paradoxical TE-IRIS from recurrence of disease due to inadequate secondary Toxoplasma prophylaxis. There was no difference in time between start of TE treatment and cART initiation for patients who did or did not develop paradoxical TE-IRIS (p = 0.50). Within the group of 2228 patients who started cART while having a CD4 count below 200?×?10/L and receiving adequate primary prophylaxis, we identified eight cases of unmasking TE-IRIS (0.36%). Unmasking TE-IRIS could not be differentiated from a newly occurring TE in six other patients, as they were not receiving adequate primary prophylaxis against Toxoplasma. CONCLUSION:: Unmasking TE-IRIS was rare in this cohort, whereas paradoxical TE-IRIS did occur more often. We found no relationship between the timing of cART initiation and the occurrence of paradoxical TE-IRIS.
AB - OBJECTIVES:: To investigate the incidence and risk factors of immune reconstitution inflammatory syndrome (IRIS) associated with toxoplasmic encephalitis (TE) in patients starting cART. DESIGN:: A historical multicenter cohort study. METHODS:: We included all HIV-infected patients diagnosed with TE in six Dutch hospitals between 1996 and 2016. Diagnosis of TE-IRIS was made using predefined IRIS criteria. We distinguished paradoxical TE-IRIS (worsening of underlying treated infection) from unmasking TE-IRIS (unmasking of subclinical infection after start of cART). We compared CD4 count, plasma viral load and timing of cART initiation between patients with and without paradoxical TE-IRIS. RESULTS:: 211 TE cases were included. Among 143 cases at risk for paradoxical TE-IRIS, we identified five cases of paradoxical TE-IRIS (3.5%). In six other cases we could not differentiate paradoxical TE-IRIS from recurrence of disease due to inadequate secondary Toxoplasma prophylaxis. There was no difference in time between start of TE treatment and cART initiation for patients who did or did not develop paradoxical TE-IRIS (p = 0.50). Within the group of 2228 patients who started cART while having a CD4 count below 200?×?10/L and receiving adequate primary prophylaxis, we identified eight cases of unmasking TE-IRIS (0.36%). Unmasking TE-IRIS could not be differentiated from a newly occurring TE in six other patients, as they were not receiving adequate primary prophylaxis against Toxoplasma. CONCLUSION:: Unmasking TE-IRIS was rare in this cohort, whereas paradoxical TE-IRIS did occur more often. We found no relationship between the timing of cART initiation and the occurrence of paradoxical TE-IRIS.
KW - antiretroviral therapy
KW - HIV
KW - immune reconstitution inflammatory syndrome
KW - Netherlands
KW - toxoplasma
UR - http://www.scopus.com/inward/record.url?scp=85017182150&partnerID=8YFLogxK
U2 - 10.1097/QAD.0000000000001492
DO - 10.1097/QAD.0000000000001492
M3 - Article
C2 - 28375874
AN - SCOPUS:85017182150
SN - 0269-9370
VL - 31
SP - 1415
EP - 1424
JO - AIDS
JF - AIDS
IS - 10
ER -