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. Author manuscript; available in PMC: 2020 Jun 1.
Published in final edited form as: Semin Arthritis Rheum. 2018 Nov 3;48(6):1087–1092. doi: 10.1016/j.semarthrit.2018.10.018

Table 2.

PJP prophylaxis patterns among patients with new immunosuppressant drug starts, stratified by anchor immunosuppressant.

Anchor
immunossupressant
Specific drug bundle N Yes
prophylaxis
% No
prophylaxis
%
Highest risk Cyclophosphamide (CYC) 30 23 77% 7 23%
CYC alone 8 5 3
CYC + high-dose GC 13 9 4
CYC + Rituximab 9 9 0
Rituximab 41 28 68% 13 32%
Intermediate risk Rituximab alone 13 11 2
Rituximab + GC 23 16 7
Rituximab + other(s) 5 1 4
High-dose glucocorticoids (GC) 94 37 39% 57 61%
High-dose GC alone 27 5 22
High-dose GC + MMF 51 21 30
High-dose GC + other(s) 16 11 5
Lower risk Mycophenolate mofetil (MMF) 71 15 21% 56 79%
MMFalone 19 1 18
MMF + GC 48 14 34
MMF + other(s) 4 0 4
Azathioprine (AZA) 33 11 33% 22 67%
AZA alone 6 2 4
AZA + GC 27 9 18
Methotrexate (MTX) 47 10 21% 37 79%
MTX alone 14 1 13
MTX + GC 33 9 24

Anchor immunosuppresant: we created a hierarchy of drugs in order to categorize drug combinations according to risk of drug-conferred risk of PJP in the following order: cyclophosphamide (highest risk), rituximab, high-dose GC, MMF, AZA, and MTX (lowest risk).