The antipyretic efficacy and safety of propacetamol compared with dexibuprofen in febrile children: a multicenter, randomized, double-blind, comparative, phase 3 clinical trial

被引:15
|
作者
Choi, Seung Jun [1 ,2 ]
Moon, Sena [3 ]
Choi, Ui Yoon [3 ]
Chun, Yoon Hong [3 ]
Lee, Jung Hyun [3 ]
Rhim, Jung Woo [3 ]
Lee, Jin [4 ]
Kim, Hwang Min [5 ]
Jeong, Dae Chul [3 ,6 ]
机构
[1] Univ Ulsan, Childrens Hosp, Asan Med Ctr, Dept Pediat,Coll Med, Seoul, South Korea
[2] Catholic Univ Korea, Coll Med, Grad Sch Med, Seoul, South Korea
[3] Catholic Univ Korea, Coll Med, Dept Pediat, 222 Banpodaero, Seoul 06591, South Korea
[4] Hanjin Gen Hosp, Dept Pediat, Seoul, South Korea
[5] Yonsei Christian Hosp, Dept Pediat, Wonju, South Korea
[6] Catholic Univ Korea, Coll Med, Vaccine Biores Inst, Seoul, South Korea
来源
BMC PEDIATRICS | 2018年 / 18卷
关键词
Children; Dexibuprofen; Fever; Propacetamol; Upper respiratory tract infection; RESPIRATORY-TRACT INFECTION; PARACETAMOL; IBUPROFEN; ACETAMINOPHEN; FEVER; PHARMACOKINETICS; ANALGESIA; TOLERANCE; THERAPY; PYREXIA;
D O I
10.1186/s12887-018-1166-z
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: We aimed to compare the antipyretic efficacy, safety, and tolerability between oral dexibuprofen and intravenous propacetamol in children with upper respiratory tract infection (URTI) presenting with fever. Methods: Patients aging from 6 months to 14 years admitted for URTI with axillary body temperature >= 38.0 degrees C were enrolled and randomized into the study or control group. Patients in the study group were intravenously infused with propacetamol and subsequently oral placebo medication was administered. Patients in the control group were intravenously infused with 100 mL of 0.9% sodium chloride solution without propacetamol and then oral dexibuprofen was administered. We checked the body temperature of all patients at 0.5 h (hr), 1 h, 1.5 h, 2 h, 3 h, 4 h, and 6 h after oral placebo or dexibuprofen had been applied. Results: A total of 263 patients (125 in the study group) were finally enrolled. The body temperatures of patients in the study group were significantly lower until 2 h after administration (37.73 +/- 0.58 vs 38.36 +/- 0.69 degrees C (p < 0.001), 37. 37 +/- 0.53 vs 37.88 +/- 0.69 degrees C (p < 0.001), 37.27 +/- 0.60 vs 37.62 +/- 0.66 degrees C (p < 0.001), 37.25 +/- 0.62 vs 37.40 +/- 0.60 degrees C (p = 0.0452), at 0.5 h, 1 h, 1.5 h, and 2 h, respectively). The two groups showed no significant differences in terms of the range of body temperature decrease, the Area Under the Curve of body temperature change for antipyretic administration-and-time relationship, the maximum value of body temperature decrease during the 6 h test period, the number of patients whose body temperature normalized (< 37.0 degrees C), the mean time when first normalization of body temperature, and the development of adverse events including gastrointestinal problem, elevated liver enzyme, and thrombocytopenia. Conclusions: Intravenous propacetamol may be a safe and effective choice for pediatric URTI patients presenting with fever who are not able to take oral medications or need faster fever control.
引用
收藏
页数:7
相关论文
共 50 条
  • [1] The antipyretic efficacy and safety of propacetamol compared with dexibuprofen in febrile children: a multicenter, randomized, double-blind, comparative, phase 3 clinical trial
    Seung Jun Choi
    Sena Moon
    Ui Yoon Choi
    Yoon Hong Chun
    Jung Hyun Lee
    Jung Woo Rhim
    Jin Lee
    Hwang Min Kim
    Dae Chul Jeong
    BMC Pediatrics, 18
  • [2] Antipyretic efficacy and tolerability of a single intravenous dose of the acetaminophen prodrug propacetamol in children: A randomized, double-blind, placebo-controlled trial
    Walson, Philip D.
    Jones, Jim
    Chesney, Russell
    Rodarte, Alexander
    CLINICAL THERAPEUTICS, 2006, 28 (05) : 762 - 769
  • [3] Antipyretic Efficacy and Safety of Ibuprofen Versus Acetaminophen Suspension in Febrile Children: Results of 2 Randomized, Double-Blind, Single-Dose Studies
    Jayawardena, Shyamalie
    Kellstein, David
    CLINICAL PEDIATRICS, 2017, 56 (12) : 1120 - 1127
  • [4] Double-blind, randomized clinical trial for safety and efficacy of norfloxacin for shigellosis in children
    Bhattacharya, SK
    Bhattacharya, MK
    Dutta, D
    Dutta, S
    Deb, M
    Deb, A
    Das, KP
    Koley, H
    Nair, GB
    ACTA PAEDIATRICA, 1997, 86 (03) : 319 - 320
  • [5] Efficacy and safety of Qinxiang Qingjie oral solution for the treatment of influenza in children: a randomized, double-blind, multicenter clinical trial
    Hu, Siyuan
    Ma, Rong
    Shen, Kunling
    Xin, Deli
    Li, Xinmin
    Xu, Baoping
    Zhao, Xiaobing
    Feng, Ziwei
    Yan, Yongbin
    Xue, Zheng
    Zhang, Baoqing
    Li, Xueming
    Zheng, Yanmei
    Zhou, Hongxia
    Wu, Liqun
    Yang, Lili
    Xu, Hua
    Shao, Rongchang
    Yin, Yong
    Zhong, Chengliang
    Li, Han
    Cai, Qiuhan
    Xu, Yaqian
    TRANSLATIONAL PEDIATRICS, 2022, 11 (06) : 987 - +
  • [6] Comparative evaluation of the efficacy of intravenous paracetamol and ibuprofen on the treatment of tonsillopharyngitis with fever: A prospective, randomized controlled, double-blind clinical trial
    Oncel, Gizem
    Yilmaz, Atakan
    Sabirli, Ramazan
    Cimen, Yesim Kinaci
    Ozen, Mert
    Seyit, Murat
    Turkcuer, Ibrahim
    Cimen, Uzeyir
    TURKISH JOURNAL OF EMERGENCY MEDICINE, 2021, 21 (04): : 177 - 183
  • [7] The Efficacy and Safety of Pelubiprofen in the Treatment of Acute Upper Respiratory Tract Infection: A Multicenter, Randomized, Double-Blind, Non-Inferiority Phase III Clinical Trial Compared to Loxoprofen
    Jang, An Soo
    Kim, Sang Hoon
    Lee, Sang Pyo
    Na, Moon Jun
    Yoo, Kwang Ha
    Park, Chang Han
    Park, Seong Yeon
    Choi, Byoung Whui
    JOURNAL OF CLINICAL MEDICINE, 2025, 14 (05)
  • [8] Efficacy and Safety of Olanzapine in Children Receiving Highly Emetogenic Chemotherapy: A Randomized, Double-blind Placebo-controlled Phase 3 Trial
    Moothedath, Abdul W.
    Meena, Jagdish P.
    Gupta, Aditya K.
    Velpandian, Thirumurthy
    Pandey, Ravindra M.
    Seth, Rachna
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2022, 44 (08) : 446 - 453
  • [9] Efficacy and safety of herbal medicine (Binafuxi granules) for the common cold with fever: A multicenter, randomized, double-blind, placebo-controlled, phase II clinical trial
    Liu, Xuemei
    Min, Jie
    She, Bin
    Chen, Yan
    Li, Jun
    Huang, Lei
    Chen, Ju
    Luo, Ai
    Yang, Mei
    Li, Ting
    Wu, Yanqing
    Chen, Daohong
    Zhong, Hongli
    Liu, Wei
    Mao, Bing
    Jiang, Hongli
    INTEGRATIVE MEDICINE RESEARCH, 2023, 12 (03)
  • [10] Results of a randomized double-blind multicenter clinical trial of the efficacy and safety of the drug riamilovir for the prevention of COVID-19
    Sabitov, Alebai U.
    Lioznov, Dmitry A.
    Zhdanov, Konstantin V.
    Tihonova, Elena P.
    Esaulenko, Elena V.
    Sorokin, Pavel V.
    TERAPEVTICHESKII ARKHIV, 2024, 96 (03) : 280 - 285