TY - JOUR
T1 - Characteristics of Japanese patients with non-dialysis-dependent chronic kidney disease initiating treatment for anemia
T2 - a retrospective real-world database study
AU - Kokado, Yoshimasa
AU - Ishii, Manabu
AU - Ueta, Kiichiro
AU - Yamamoto, Hiroyuki
AU - Kumamaru, Hiraku
AU - Isshiki, Masaaki
AU - Demiya, Sven
AU - Miyata, Hiroaki
N1 - Funding Information:
This study was funded by Mitsubishi Tanabe Pharma Corporation Ltd. The sponsor funded the medical writing for preparation of the manuscript.
Funding Information:
Y.K., M.Ish. and K.U. have disclosed that they are employed by Mitsubishi Tanabe Pharma Corporation. M.Iss. and S.D. have disclosed that they are employed by IQVIA Solutions Japan KK. H.Y., H.K. and H.M. have disclosed that they received consultant fees from Mitsubishi Tanabe Pharma Corporation for this research project and are affiliated with the Department of Healthcare Quality Assessment at the University of Tokyo, which is a social collaboration program supported by National Clinical Database, Johnson & Johnson KK and Nipro Corporation. CMRO peer reviewers on this manuscript have no relevant financial or other relationships to disclose.
Funding Information:
The authors thank Krishant Chand of IQVIA Solutions Japan KK for performing data analyses and manuscript preparation. We also thank International Medical Translation Service Inc. for manuscript writing and editorial assistance.
Publisher Copyright:
© 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022
Y1 - 2022
N2 - Objective: Anemia is a common complication of chronic kidney disease (CKD). The aim of this study was to evaluate hemoglobin levels at the initiation of erythropoiesis stimulating agent (ESA) therapy in patients with non-dialysis-dependent CKD (NDD-CKD) and anemia using a large-scale administrative database in Japan. Methods: The longitudinal data of adult patients who initiated ESA therapy between April 2008 and December 2018 were extracted from a hospital-based administrative database. The primary outcome was hemoglobin level at the initiation of ESA therapy, whereas the exploratory outcome was hemoglobin level recorded 6 months after the onset of the ESA therapy. Results: A total of 4939 patients were included in the primary analysis. The mean hemoglobin level at the initiation of ESA therapy was 9.1 g/dL, which was lower than the level (11 g/dL) recommended for the initiation of treatment by the current Japanese treatment guidelines. Moreover, 42.1% and 15.0% of the patients had hemoglobin levels <9.0 and <8.0 g/dL, respectively, at the initiation of ESA therapy. In 2964 patients for whom hemoglobin levels at 6 months after the initiation of ESA therapy were available, the mean hemoglobin level increased to 10.3 g/dL, and 61.9% and 31.1% of these patients had hemoglobin levels ≥10.0 and ≥11.0 g/dL, respectively. Conclusion: This real-world database study revealed that hemoglobin levels at the initiation of ESA therapy in new users of ESA were lower than those recommended by treatment guidelines in Japan.
AB - Objective: Anemia is a common complication of chronic kidney disease (CKD). The aim of this study was to evaluate hemoglobin levels at the initiation of erythropoiesis stimulating agent (ESA) therapy in patients with non-dialysis-dependent CKD (NDD-CKD) and anemia using a large-scale administrative database in Japan. Methods: The longitudinal data of adult patients who initiated ESA therapy between April 2008 and December 2018 were extracted from a hospital-based administrative database. The primary outcome was hemoglobin level at the initiation of ESA therapy, whereas the exploratory outcome was hemoglobin level recorded 6 months after the onset of the ESA therapy. Results: A total of 4939 patients were included in the primary analysis. The mean hemoglobin level at the initiation of ESA therapy was 9.1 g/dL, which was lower than the level (11 g/dL) recommended for the initiation of treatment by the current Japanese treatment guidelines. Moreover, 42.1% and 15.0% of the patients had hemoglobin levels <9.0 and <8.0 g/dL, respectively, at the initiation of ESA therapy. In 2964 patients for whom hemoglobin levels at 6 months after the initiation of ESA therapy were available, the mean hemoglobin level increased to 10.3 g/dL, and 61.9% and 31.1% of these patients had hemoglobin levels ≥10.0 and ≥11.0 g/dL, respectively. Conclusion: This real-world database study revealed that hemoglobin levels at the initiation of ESA therapy in new users of ESA were lower than those recommended by treatment guidelines in Japan.
KW - Anemia
KW - chronic kidney disease
KW - erythropoiesis stimulating agent
KW - hemoglobin
KW - non-dialysis
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U2 - 10.1080/03007995.2022.2125256
DO - 10.1080/03007995.2022.2125256
M3 - Article
C2 - 36111421
AN - SCOPUS:85139976894
VL - 38
SP - 2175
EP - 2182
JO - Current Medical Research and Opinion
JF - Current Medical Research and Opinion
SN - 0300-7995
IS - 12
ER -