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Prednisone plus IVIg compared with prednisone or IVIg for immune thrombocytopenia in pregnancy: a national retrospective cohort study.
Zhu, Xiao-Lu; Feng, Ru; Huang, Qiu-Sha; Liang, Mei-Ying; Jiang, Ming; Liu, Hui; Liu, Yi; Yao, Hong-Xia; Zhang, Lei; Qian, Shen-Xian; Yang, Tong-Hua; Zhang, Jing-Yu; Shen, Xu-Liang; Yang, Lin-Hua; Hu, Jian-Da; Huang, Ren-Wei; Jiang, Zhong-Xing; Wang, Jing-Wen; Zhang, Hong-Yu; Xiao, Zhen; Zhan, Si-Yan; Liu, Hui-Xin; Wang, Xing-Lin; Chang, Ying-Jun; Wang, Yu; Kong, Yuan; Xu, Lan-Ping; Liu, Kai-Yan; Zhang, Xiao-Hong; Yin, Cheng-Hong; Li, Yue-Ying; Wang, Qian-Fei; Wang, Jian-Liu; Huang, Xiao-Jun; Zhang, Xiao-Hui.
Afiliação
  • Zhu XL; Peking University People's Hospital, Beijing, P.R. China.
  • Feng R; Departments of Hematology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, P.R. China.
  • Huang QS; Peking University People's Hospital, Beijing, P.R. China.
  • Liang MY; Department of Obstetrics and Gynecology, Peking University People's Hospital, Beijing, P.R. China.
  • Jiang M; Center of Hematologic Diseases, First Affiliated Hospital of Xinjiang Medical University, Ürümqi, P.R. China.
  • Liu H; Departments of Hematology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, P.R. China.
  • Liu Y; Department of Hematology, Navy General Hospital, Beijing, P.R. China.
  • Yao HX; Department of Hematology, People's Hospital of Hainan Province, Haikou, P.R. China.
  • Zhang L; State Key Laboratory of Experimental Hematology, Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, P.R. China.
  • Qian SX; Department of Hematology, First People's Hospital of Hangzhou, Hangzhou, P.R. China.
  • Yang TH; Department of Hematology, First People's Hospital of Yunnan Province, Kunming, P.R. China.
  • Zhang JY; Department of Hematology, Hebei Institute of Hematology, The Second Hospital of Hebei Medical University, Shijiazhuang, P.R. China.
  • Shen XL; Department of Hematology, He Ping Central Hospital of the Changzhi Medical College, Changzhi, P.R. China.
  • Yang LH; Department of Hematology, Second Hospital of Shanxi Medical University, Taiyuan, P.R. China.
  • Hu JD; Fujian Institute of Hematology, Fujian Provincial Key Laboratory of Hematology, Fujian Medical University Union Hospital, Fuzhou, P.R. China.
  • Huang RW; Department of Hematology, Third Affiliated Hospital of Southern Medical University, Guangzhou, P.R. China.
  • Jiang ZX; Department of Hematology, First Affiliated Hospital of Zhengzhou University, Zhengzhou, P.R. China.
  • Wang JW; Department of Hematology, Beijing Tongren Hospital, Beijing, P.R. China.
  • Zhang HY; Department of Hematology, Peking University Shenzhen Hospital, Shenzhen, P.R. China.
  • Xiao Z; Department of Hematology, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, P.R. China.
  • Zhan SY; Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing, P.R. China.
  • Liu HX; Department of Clinical Epidemiology, Peking University People's Hospital, Beijing, P.R. China.
  • Wang XL; Peking University People's Hospital, Beijing, P.R. China.
  • Chang YJ; Peking University People's Hospital, Beijing, P.R. China.
  • Wang Y; Peking University People's Hospital, Beijing, P.R. China.
  • Kong Y; Peking University People's Hospital, Beijing, P.R. China.
  • Xu LP; Peking University People's Hospital, Beijing, P.R. China.
  • Liu KY; Peking University People's Hospital, Beijing, P.R. China.
  • Zhang XH; Department of Obstetrics and Gynecology, Peking University People's Hospital, Beijing, P.R. China.
  • Yin CH; Department of Internal Medicine, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, P.R. China.
  • Li YY; CAS Key Laboratory of Genomic and Precision Medicine, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences, China National Center for Bioinformation, Beijing, P.R. China.
  • Wang QF; CAS Key Laboratory of Genomic and Precision Medicine, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences, China National Center for Bioinformation, Beijing, P.R. China.
  • Wang JL; Department of Obstetrics and Gynecology, Peking University People's Hospital, Beijing, P.R. China.
  • Huang XJ; Peking University People's Hospital, Beijing, P.R. China.
  • Zhang XH; Peking University People's Hospital, Peking University Institute of Hematology, No. 11 Xizhimen South Street, Xicheng District, Beijing 100044, P.R. China.
Ther Adv Hematol ; 13: 20406207221095226, 2022.
Article em En | MEDLINE | ID: mdl-35510211
Background: The responses of intravenous immunoglobulin (IVIg) or corticosteroids as the initial treatment on pregnancy with ITP were unsatisfactory. This study aimed to assess the safety and effectiveness of prednisone plus IVIg versus prednisone or IVIg in pregnant patients with immune thrombocytopenia (ITP). Methods: Between 1 January 2010 and 31 December 2020, 970 pregnancies diagnosed with ITP at 19 collaborative centers in China were reviewed in this observational study. A total of 513 pregnancies (52.89%) received no intervention. Concerning the remaining pregnancies, 151 (33.04%) pregnancies received an initial treatment of prednisone plus IVIg, 105 (22.98%) pregnancies received IVIg alone, and 172 (37.64%) pregnancies only received prednisone. Results: Regarding the maternal response to the initial treatment, no differences were found among the three treatment groups (41.1% for prednisone plus IVIg, 33.1% for prednisone, and 38.1% for IVIg). However, a significant difference was observed in the time to response between the prednisone plus IVIg group (4.39 ± 2.54 days) and prednisone group (7.29 ± 5.01 days; p < 0.001), and between the IVIg group (6.71 ± 4.85 days) and prednisone group (p < 0.001). The median prednisone duration in the monotherapy group was 27 days (range, 8-195 days), whereas that in the combination group was 14 days (range, 6-85 days). No significant differences were found among these three treatment groups in neonatal outcomes, particularly concerning the neonatal platelet counts. The time to response in the combination treatment group was shorter than prednisone monotherapy. The duration of prednisone application in combination group was shorter than prednisone monotherapy. The combined therapy showed a lower predelivery platelet transfusion rate than IVIg alone. Conclusion: These findings suggest that prednisone plus IVIg may represent a potential combination therapy for pregnant patients with ITP.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article