Efficacy and safety of alternating norfloxacin and rifaximin as primary prophylaxis for spontaneous bacterial peritonitis in cirrhotic ascites: a prospective randomized open-label comparative multicenter study

被引:51
作者
Assem, M. [1 ]
Elsabaawy, M. [1 ]
Abdelrashed, M. [2 ]
Elemam, S. [3 ]
Khodeer, S. [4 ]
Hamed, W. [5 ]
Abdelaziz, A. [6 ]
El-Azab, G. [1 ]
机构
[1] Menoufia Univ, Natl Liver Inst, Hepatol Dept, Menoufia 52311, Egypt
[2] Al Noor Hosp, MOH, Dept Internal Med, Mecca, Saudi Arabia
[3] King Khalid Hosp, MOH, Dept Trop Med, Tabuk, Saudi Arabia
[4] Tanta Univ, Fac Med, Dept Internal Med, Tanta, Egypt
[5] Ain Shams Univ, Fac Med, Dept Trop Med, Cairo, Egypt
[6] Menoufia Univ, Natl Liver Inst, Dept Clin Pathol, Menoufia 52311, Egypt
关键词
Spontaneous bacterial peritonitis; Norfloxacin; Rifaximin; Primary prophylaxis; HEPATORENAL-SYNDROME; PREDICTIVE FACTORS; INTESTINAL DECONTAMINATION; PROTEIN-CONCENTRATION; CONSENSUS CONFERENCE; RENAL IMPAIRMENT; LIVER-CIRRHOSIS; DIAGNOSIS; MANAGEMENT; ALBUMIN;
D O I
10.1007/s12072-015-9688-z
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Primary prevention of spontaneous bacterial peritonitis (SBP) is an important strategy to reduce morbidity and mortality in cirrhotic patients with ascites. Efficacy and safety of alternating rifaximin and norfloxacin as primary prophylaxis is questionable. Three hundred thirty-four cirrhotic patients with high SAAG (a parts per thousand yen1.1) ascites, protein level in ascitic fluid less than 1.5 g/dL with advanced liver disease (Child-Pugh score > 9 points with serum bilirubin level > 3 mg/dL) or renal impairment (serum creatinine level > 1.2 mg/dL, blood urea nitrogen level > 25 mg/dL, or serum sodium level < 130 mEq/L) were included in an open-label, randomized study aimed at comparing alternating use of norfloxacin and rifaximin vs. norfloxacin or rifaximin alone as primary prophylaxis for SBP. Both intention-to-treat and per-protocol efficacy analyses were done after 6 months of treatment by assessment of ascitic fluid neutrophil count. Safety analysis was done for all intention-to-treat populations. Alternating norfloxacin and rifaximin showed superior prophylaxis by intention-to-treat (74.7 vs. 56.4 % vs. 68.3 %, p < 0.048). Pairwise analysis showed that alternating regimen had lower probability to develop SBP when compared to a norfloxacin-based regimen in intention-to-treat (p = 0.016) and per protocol analysis (p = 0.039). There was no difference among the studied groups regarding the incidence and severity of adverse events reported. Alternating norfloxacin- and rifaximin-based primary prophylaxis for SBP showed higher efficacy with the same safety profile when compared with monotherapy of norfloxacin.
引用
收藏
页码:377 / 385
页数:9
相关论文
共 28 条
  • [21] Efficacy and safety of ferric citrate on hyperphosphatemia among Chinese patients with chronic kidney disease undergoing hemodialysis: a phase III multicenter randomized open-label active-drug controlled study
    Wang, Yong
    Chen, Xiangmei
    Zhu, Hanyu
    Guo, Zhiyong
    Yang, Yibin
    Luo, Ping
    He, Yani
    Xu, Yan
    Ji, Daxi
    Gao, Xinlu
    Sun, Xiuli
    Xing, Changying
    Wang, Yu
    Wang, Xiaohui
    Zhao, Shuping
    Guan, Yan
    Lin, Hongli
    Zhong, Aimin
    Shui, Hua
    Shao, Fengmin
    Lv, Lu
    Yan, Yuehong
    Sun, Xiaokun
    Zhang, Lei
    AMERICAN JOURNAL OF NEPHROLOGY, 2023, 54 (11-12) : 479 - 488
  • [22] Efficacy and safety of combination therapy with mirodenafil and α1-blocker for benign prostatic hyperplasia-induced lower urinary tract symptoms accompanied by erectile dysfunction: a multicenter, open-label, prospective study
    Lee, J. Y.
    Cho, S. Y.
    Oh, C. Y.
    Ha, U. S.
    Lee, S. H.
    Park, S. Y.
    Moon, H. S.
    Lee, S. W.
    INTERNATIONAL JOURNAL OF IMPOTENCE RESEARCH, 2011, 23 (06) : 249 - 256
  • [23] Effects on agitation with rivastigmine patch monotherapy and combination therapy with memantine in mild to moderate Alzheimer's disease: a multicenter 24-week prospective randomized open-label study (the Korean EXelon Patch and combination with mEmantine Comparative Trial study)
    Yoon, Soo J.
    Choi, Seong H.
    Na, Hae R.
    Park, Kyung-Won
    Kim, Eun-Joo
    Han, Hyun J.
    Lee, Jae-Hong
    Shim, Young S.
    Na, Duk L.
    GERIATRICS & GERONTOLOGY INTERNATIONAL, 2017, 17 (03) : 494 - 499
  • [24] I-ADD Study: Assessment of Efficacy and Safety Profile of Irbesartan/Amlodipine Fixed-Dose Combination Therapy Compared With Irbesartan Monotherapy in Hypertensive Patients Uncontrolled With Irbesartan 150 mg Monotherapy: A Multicenter, Phase III, Prospective, Randomized, Open-Label With Blinded End Point Evaluation Study
    Bobrie, Guillaume
    CLINICAL THERAPEUTICS, 2012, 34 (08) : 1720 - 1734
  • [25] I-COMBINE Study: Assessment of Efficacy and Safety Profile of Irbesartan/Amlodipine Fixed-Dose Combination Therapy Compared With Amlodipine Monotherapy in Hypertensive Patients Uncontrolled With Amlodipine 5 mg Monotherapy: A Multicenter, Phase III, Prospective, Randomized, Open-Label With Blinded-End Point Evaluation Study
    Bobrie, Guillaume
    CLINICAL THERAPEUTICS, 2012, 34 (08) : 1705 - 1719
  • [26] Efficacy and safety of margetuximab plus chemotherapy vs. trastuzumab plus chemotherapy in Chinese patients with pretreated HER2-positive advanced metastatic breast cancer: results from a randomized, open-label, multicenter, phase II bridging study
    Zhang, Qingyuan
    Ouyang, Quchang
    Li, Wei
    Chiu, Joanne
    Yan, Min
    Lu, Yen-Shen
    Sun, Sanyuan
    Li, Huiping
    Du, Yingying
    Wang, Xujuan
    Sun, Tao
    Yin, Yongmei
    Wang, Haibo
    Ye, Feng
    Shen, Kunwei
    Wang, Jingfen
    Pan, Yueyin
    Wang, Shusen
    Yang, Jin
    Wu, Xiaohong
    Dai, Ming-Shen
    Cheng, Jing
    Teng, Yuee
    Su, Fang
    Wu, Xinhong
    He, Jingdong
    Fu, Peifen
    Yang, Lulu
    Xin, Yuan
    Wang, Xiaojia
    Jiang, Zefei
    TRANSLATIONAL BREAST CANCER RESEARCH, 2022, 3
  • [27] Long-term efficacy and safety of oxycodone-naloxone prolonged-release formulation (up to 180/90 mg daily) - results of the open-label extension phase of a phase III multicenter, multiple-dose, randomized, controlled study
    Dupoiron, D.
    Stachowiak, A.
    Loewenstein, O.
    Ellery, A.
    Kremers, W.
    Bosse, B.
    Hopp, M.
    EUROPEAN JOURNAL OF PAIN, 2017, 21 (09) : 1485 - 1494
  • [28] Efficacy and safety of selective JAK 1 inhibitor filgotinib in active rheumatoid arthritis patients with inadequate response to methotrexate: comparative study with filgotinib and tocilizumab examined by clinical index as well as musculoskeletal ultrasound assessment (TRANSFORM study): study protocol for a randomized, open-label, parallel-group, multicenter, and non-inferiority clinical trial
    Shimizu, Toshimasa
    Kawashiri, Shin-ya
    Morimoto, Shimpei
    Kawazoe, Yurika
    Kuroda, Shohei
    Kawasaki, Rina
    Ito, Yasuko
    Kiya, Rieko
    Sato, Shuntaro
    Yamamoto, Hiroshi
    Kawakami, Atsushi
    TRIALS, 2023, 24 (01)