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DOI 10.2169/internalmedicine.51.7418

Медицинская библиотека · Internal medicine (Tokyo, Japan) · 2012

Risk assessment for acute kidney injury after allogeneic hematopoietic stem cell transplantation based on Acute Kidney Injury Network criteria.

Mori Jinichi, Ohashi Kazuteru, Yamaguchi Takuhiro, Ando Minoru, Hirashima Yuka, Kobayashi Takeshi, Kakihana Kazuhiko, Sakamaki Hisashi

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Аннотация

OBJECTIVE

This is a retrospective study for risk assessment of acute kidney injury after allogeneic hematopoietic stem cell transplantation (allo HSCT) based on the Acute Kidney Injury Network (AKIN) criteria.

METHODS

Two hundred and eighty-nine consecutive patients who received allo HSCT were studied retrospectively to identify the risk factors for AKI according to the AKIN criteria. The incidence of AKI based on AKIN staging and overall survival (OS) was evaluated using Cox proportional hazard regression models treating each AKIN stage as a time-dependent covariate.

PATIENTS: We identified a total of 180 patients who developed AKI within 100 days after allo HSCT; AKI was classified as stage 1 in 88 patients (30.5%), stage 2 in 46 patients (15.9%) and stage 3 in 46 patients (15.9%).

RESULTS

Patients who developed stage 3 AKI had a significantly worse survival compared to those who developed no AKI or lower stage AKI (HR: 7.6, 95%CI: 4.8-12.1; p<0.001). Multivariate analysis for risks for developing AKI revealed an episode of sepsis or sinusoidal obstruction syndrome (SOS) and the use of liposomal amphotericin as a major cause of the severe stage of AKI.

CONCLUSION

On the basis of our analysis, sepsis, hemorrhagic cystitis, and acute GVHD were associated with severe AKI, and SOS was associated any stage of AKI.

Для цитирования: Mori Jinichi, Ohashi Kazuteru, Yamaguchi Takuhiro, Ando Minoru, Hirashima Yuka, Kobayashi Takeshi, Kakihana Kazuhiko, Sakamaki Hisashi. Risk assessment for acute kidney injury after allogeneic hematopoietic stem cell transplantation based on Acute Kidney Injury Network criteria.. Internal medicine (Tokyo, Japan). 2012. DOI: 10.2169/internalmedicine.51.7418.

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