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Late-onset Pneumocystis jirovecii pneumonia post-allogeneic stem cell transplantation after time-dependent discontinuation of prophylaxis.
Stavi, Vered; Desai, Nihar; Michelis, Fotios V; Kim, Dennis Dong Hwan; Kumar, Rajat; Lipton, Jeffrey Howard; Law, Arjun Datt.
Affiliation
  • Stavi V; Hans Messner Allogeneic Blood and Marrow Transplant Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
  • Desai N; Allogeneic Transplant Unit, Soroka University Medical Centre, Beersheba, Israel.
  • Michelis FV; Hans Messner Allogeneic Blood and Marrow Transplant Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
  • Kim DDH; Hans Messner Allogeneic Blood and Marrow Transplant Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
  • Kumar R; Hans Messner Allogeneic Blood and Marrow Transplant Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
  • Lipton JH; Hans Messner Allogeneic Blood and Marrow Transplant Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
  • Law AD; Hans Messner Allogeneic Blood and Marrow Transplant Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Eur J Haematol ; 112(3): 433-438, 2024 Mar.
Article in En | MEDLINE | ID: mdl-37947314
ABSTRACT

INTRODUCTION:

Pneumocystis jirovecii pneumonia (PJP) is a rare complication of hematopoietic stem cell transplantation (HSCT). Primary prophylaxis for 6-12 months post-HSCT is the standard approach. However, there is no consensus regarding the optimal duration of prophylaxis.

METHODS:

We identified patients who developed PJP more than 1-year post-HSCT. All patients had previously received 12 months of PJP prophylaxis. PJP was diagnosed based on clinical findings and the detection of P. jirovecii in bronchoalveolar lavage (BAL) using polymerase chain reaction (PCR). The CD4+ T-cell percentage was determined using flow cytometry. Data expressed as median (interquartile range).

RESULTS:

Ten patients developed PJP at 17.5 months (16-24 months) post-HSCT. PJP diagnosis occurred 5.5 months (3-15 months) after discontinuing prophylaxis. Eight patients received anti-thymocyte globulin (ATG) as graft versus host disease (GVHD) prophylaxis. At diagnosis, only one patient had lymphopenia; all patients had CD4+ T-lymphocyte counts ≥0.2 × 109 /L (median 0.337 × 109 /L). Three patients had concomitant bacterial infections. The clinical presentation was mild; only three required hospitalization, none of them required intensive care and there were no deaths.

CONCLUSION:

There is a need to develop risk-adapted prophylactic strategies in the contemporary era using ATG-based GVHD prophylaxis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia, Pneumocystis / Hematopoietic Stem Cell Transplantation / Pneumocystis carinii / Graft vs Host Disease Limits: Humans Language: En Journal: Eur J Haematol Journal subject: HEMATOLOGIA Year: 2024 Document type: Article Affiliation country: Canada Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia, Pneumocystis / Hematopoietic Stem Cell Transplantation / Pneumocystis carinii / Graft vs Host Disease Limits: Humans Language: En Journal: Eur J Haematol Journal subject: HEMATOLOGIA Year: 2024 Document type: Article Affiliation country: Canada Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM