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重组人血小板生成素在成人原发免疫性血小板减少症患者围手术期的应用

OBJECTIVE: To evaluate the efficacy and safety of recombinant human thrombopoietin (rhTPO) treatment for primary immune thrombocytopenia (ITP) patients during the perioperative period. METHODS: Adult ITP patients who were refractory to first-line glucocorticoid therapy and underwent selective surger...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342530/
https://www.ncbi.nlm.nih.gov/pubmed/30929384
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.03.005
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collection PubMed
description OBJECTIVE: To evaluate the efficacy and safety of recombinant human thrombopoietin (rhTPO) treatment for primary immune thrombocytopenia (ITP) patients during the perioperative period. METHODS: Adult ITP patients who were refractory to first-line glucocorticoid therapy and underwent selective surgery were enrolled to be treated with rhTPO at the dosage of 1.5×10(4)U/d subcutaneously during the perioperative period. rhTPO treatment would not be terminated until one of the following conditions occurred: ①Platelet counts met the requirement of surgery; ②Platelet counts were ≥100×10(9)/L; ③Completed the 14 days of therapy. End points of the study were surgery rate, rhTPO therapy response rate, rescue therapy rate and adverse responses. RESULTS: 42 patients were enrolled from Jan. 1, 2016 to Jun. 30, 2018. 14 were male and 28 were female. The median age was 60 (25–73) years old. There were no newly diagnosed patients. 5 patients were persistent and 37 were chronic. 27 patients completed selective surgery. The surgery rate was 64.3% (27/42). Among them, 13 patients were under local anesthesia and 14 under general anesthesia. Of 42 cases receiving rhTPO therapy. 31 patients achieved responses, The overall response rate was of 73.8%. Among them, 24 patients achieved CR. The CR ratio was 77.4% (24/31). 7 achieved response. The response ratio was 22.6% (7/31). 11 patients did not respond to rhTPO therapy. The non-response rate was 26.2% (11/42). The median time to reach CR was 7 (3–16) days. The median time to reach the peak of platelet counts were 10 (3–21) days. rhTPO was used for a median of 7 (3–14) days. The median platelet counts of patients undergoing surgery before rhTPO therapy, before surgery and at day 7 after surgery were 33 (20–89) ×10(9)/L, 125 (78–245) ×10(9)/L and 72 (30–250) ×10(9)/L, respectively. The median peak of platelet counts was 149 (101–466) ×10(9)/L. No infection, bleeding, thromboembolism and therapy-related adverse responses occurred in the patients. CONCLUSION: rhTPO for ITP patients during the perioperative period is safe and effective.
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spelling pubmed-73425302020-07-16 重组人血小板生成素在成人原发免疫性血小板减少症患者围手术期的应用 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To evaluate the efficacy and safety of recombinant human thrombopoietin (rhTPO) treatment for primary immune thrombocytopenia (ITP) patients during the perioperative period. METHODS: Adult ITP patients who were refractory to first-line glucocorticoid therapy and underwent selective surgery were enrolled to be treated with rhTPO at the dosage of 1.5×10(4)U/d subcutaneously during the perioperative period. rhTPO treatment would not be terminated until one of the following conditions occurred: ①Platelet counts met the requirement of surgery; ②Platelet counts were ≥100×10(9)/L; ③Completed the 14 days of therapy. End points of the study were surgery rate, rhTPO therapy response rate, rescue therapy rate and adverse responses. RESULTS: 42 patients were enrolled from Jan. 1, 2016 to Jun. 30, 2018. 14 were male and 28 were female. The median age was 60 (25–73) years old. There were no newly diagnosed patients. 5 patients were persistent and 37 were chronic. 27 patients completed selective surgery. The surgery rate was 64.3% (27/42). Among them, 13 patients were under local anesthesia and 14 under general anesthesia. Of 42 cases receiving rhTPO therapy. 31 patients achieved responses, The overall response rate was of 73.8%. Among them, 24 patients achieved CR. The CR ratio was 77.4% (24/31). 7 achieved response. The response ratio was 22.6% (7/31). 11 patients did not respond to rhTPO therapy. The non-response rate was 26.2% (11/42). The median time to reach CR was 7 (3–16) days. The median time to reach the peak of platelet counts were 10 (3–21) days. rhTPO was used for a median of 7 (3–14) days. The median platelet counts of patients undergoing surgery before rhTPO therapy, before surgery and at day 7 after surgery were 33 (20–89) ×10(9)/L, 125 (78–245) ×10(9)/L and 72 (30–250) ×10(9)/L, respectively. The median peak of platelet counts was 149 (101–466) ×10(9)/L. No infection, bleeding, thromboembolism and therapy-related adverse responses occurred in the patients. CONCLUSION: rhTPO for ITP patients during the perioperative period is safe and effective. Editorial office of Chinese Journal of Hematology 2019-03 /pmc/articles/PMC7342530/ /pubmed/30929384 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.03.005 Text en 2019年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 论著
重组人血小板生成素在成人原发免疫性血小板减少症患者围手术期的应用
title 重组人血小板生成素在成人原发免疫性血小板减少症患者围手术期的应用
title_full 重组人血小板生成素在成人原发免疫性血小板减少症患者围手术期的应用
title_fullStr 重组人血小板生成素在成人原发免疫性血小板减少症患者围手术期的应用
title_full_unstemmed 重组人血小板生成素在成人原发免疫性血小板减少症患者围手术期的应用
title_short 重组人血小板生成素在成人原发免疫性血小板减少症患者围手术期的应用
title_sort 重组人血小板生成素在成人原发免疫性血小板减少症患者围手术期的应用
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342530/
https://www.ncbi.nlm.nih.gov/pubmed/30929384
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.03.005
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