The longitudinal outcomes of applying non-selective beta-blockers in portal hypertension: real-world multicenter study

Background/Aim We investigated the effect of non-selective β-blockers (NSBB) in real-world situations and whether low-dose NSBB is beneficial compared to maximally tolerated doses. Methods We performed a retrospective study of 740 patients with cirrhosis requiring prophylactic treatment of esophagea...

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Vydáno v:Hepatology international Ročník 15; číslo 2; s. 424 - 436
Hlavní autoři: Kang, Seong Hee, Lee, Minjong, Kim, Moon Young, Lee, Jun Hyeok, Jun, Baek Gyu, Kim, Tae Suk, Choi, Dae Hee, Suk, Ki Tae, Kim, Young Don, Cheon, Gab Jin, Kim, Dong Joon, Baik, Soon Koo
Médium: Journal Article
Jazyk:angličtina
Vydáno: New Delhi Springer India 01.04.2021
Springer Nature B.V
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ISSN:1936-0533, 1936-0541, 1936-0541
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Abstract Background/Aim We investigated the effect of non-selective β-blockers (NSBB) in real-world situations and whether low-dose NSBB is beneficial compared to maximally tolerated doses. Methods We performed a retrospective study of 740 patients with cirrhosis requiring prophylactic treatment of esophageal varices: 473 primary prophylaxis (PP: NSBB = 349, non-NSBB = 124) and 267 secondary prophylaxis (SP: NSBB = 200, non-NSBB = 67). The NSBB group was divided into low-dose (≤ 80 mg/day) and high-dose (> 80 mg/day). Results In the PP group, NSBB treatment reduced mortality and showed the most pronounced effect in patients with moderate/severe ascites (hazard ratio [HR], 0.46; p  < 0.01), HVPG ≥ 16 mmHg (HR, 0.53; p  = 0.04), or CTP class B/C (HR, 0.46; p  < 0.01) but not in those with no/mild ascites, HVPG < 16 mmHg, or CTP class A. Low-dose NSBB group showed a significant reduction in mortality compared with non-NSBB (moderate/severe ascites: HR, 0.61; p  = 0.02 and CTP class B/C: HR, 0.41; p  < 0.01) and the effect size was stronger than the high-dose NSBB. NSBB was associated with a reduced risk of infection (HR, 0.36; p  = 0.01). In the SP group, NSBB prolonged survival in patients with moderate/severe ascites (HR, 0.56; p  = 0.02), HVPG ≥ 16 mmHg (HR, 0.42; p  < 0.01), or CTP class B/C (HR, 0.52; p  < 0.01). Low-dose NSBB was more beneficial with 56% risk reduction ( p  < 0.01) of mortality compared with 33% risk reduction in the high-dose NSBB ( p  = 0.05). Conclusion NSBB therapy was associated with longer survival in PP and SP groups who had an advanced stage of cirrhosis. Moreover, low-dose NSBB exhibited a better benefit than a standard-titrated high-dose NSBB with better tolerability.
AbstractList Background/AimWe investigated the effect of non-selective β-blockers (NSBB) in real-world situations and whether low-dose NSBB is beneficial compared to maximally tolerated doses.MethodsWe performed a retrospective study of 740 patients with cirrhosis requiring prophylactic treatment of esophageal varices: 473 primary prophylaxis (PP: NSBB = 349, non-NSBB = 124) and 267 secondary prophylaxis (SP: NSBB = 200, non-NSBB = 67). The NSBB group was divided into low-dose (≤ 80 mg/day) and high-dose (> 80 mg/day).ResultsIn the PP group, NSBB treatment reduced mortality and showed the most pronounced effect in patients with moderate/severe ascites (hazard ratio [HR], 0.46; p < 0.01), HVPG ≥ 16 mmHg (HR, 0.53; p = 0.04), or CTP class B/C (HR, 0.46; p < 0.01) but not in those with no/mild ascites, HVPG < 16 mmHg, or CTP class A. Low-dose NSBB group showed a significant reduction in mortality compared with non-NSBB (moderate/severe ascites: HR, 0.61; p = 0.02 and CTP class B/C: HR, 0.41; p < 0.01) and the effect size was stronger than the high-dose NSBB. NSBB was associated with a reduced risk of infection (HR, 0.36; p = 0.01). In the SP group, NSBB prolonged survival in patients with moderate/severe ascites (HR, 0.56; p = 0.02), HVPG ≥ 16 mmHg (HR, 0.42; p < 0.01), or CTP class B/C (HR, 0.52; p < 0.01). Low-dose NSBB was more beneficial with 56% risk reduction (p < 0.01) of mortality compared with 33% risk reduction in the high-dose NSBB (p = 0.05).ConclusionNSBB therapy was associated with longer survival in PP and SP groups who had an advanced stage of cirrhosis. Moreover, low-dose NSBB exhibited a better benefit than a standard-titrated high-dose NSBB with better tolerability.
We investigated the effect of non-selective β-blockers (NSBB) in real-world situations and whether low-dose NSBB is beneficial compared to maximally tolerated doses.BACKGROUND/AIMWe investigated the effect of non-selective β-blockers (NSBB) in real-world situations and whether low-dose NSBB is beneficial compared to maximally tolerated doses.We performed a retrospective study of 740 patients with cirrhosis requiring prophylactic treatment of esophageal varices: 473 primary prophylaxis (PP: NSBB = 349, non-NSBB = 124) and 267 secondary prophylaxis (SP: NSBB = 200, non-NSBB = 67). The NSBB group was divided into low-dose (≤ 80 mg/day) and high-dose (> 80 mg/day).METHODSWe performed a retrospective study of 740 patients with cirrhosis requiring prophylactic treatment of esophageal varices: 473 primary prophylaxis (PP: NSBB = 349, non-NSBB = 124) and 267 secondary prophylaxis (SP: NSBB = 200, non-NSBB = 67). The NSBB group was divided into low-dose (≤ 80 mg/day) and high-dose (> 80 mg/day).In the PP group, NSBB treatment reduced mortality and showed the most pronounced effect in patients with moderate/severe ascites (hazard ratio [HR], 0.46; p < 0.01), HVPG ≥ 16 mmHg (HR, 0.53; p = 0.04), or CTP class B/C (HR, 0.46; p < 0.01) but not in those with no/mild ascites, HVPG < 16 mmHg, or CTP class A. Low-dose NSBB group showed a significant reduction in mortality compared with non-NSBB (moderate/severe ascites: HR, 0.61; p = 0.02 and CTP class B/C: HR, 0.41; p < 0.01) and the effect size was stronger than the high-dose NSBB. NSBB was associated with a reduced risk of infection (HR, 0.36; p = 0.01). In the SP group, NSBB prolonged survival in patients with moderate/severe ascites (HR, 0.56; p = 0.02), HVPG ≥ 16 mmHg (HR, 0.42; p < 0.01), or CTP class B/C (HR, 0.52; p < 0.01). Low-dose NSBB was more beneficial with 56% risk reduction (p < 0.01) of mortality compared with 33% risk reduction in the high-dose NSBB (p = 0.05).RESULTSIn the PP group, NSBB treatment reduced mortality and showed the most pronounced effect in patients with moderate/severe ascites (hazard ratio [HR], 0.46; p < 0.01), HVPG ≥ 16 mmHg (HR, 0.53; p = 0.04), or CTP class B/C (HR, 0.46; p < 0.01) but not in those with no/mild ascites, HVPG < 16 mmHg, or CTP class A. Low-dose NSBB group showed a significant reduction in mortality compared with non-NSBB (moderate/severe ascites: HR, 0.61; p = 0.02 and CTP class B/C: HR, 0.41; p < 0.01) and the effect size was stronger than the high-dose NSBB. NSBB was associated with a reduced risk of infection (HR, 0.36; p = 0.01). In the SP group, NSBB prolonged survival in patients with moderate/severe ascites (HR, 0.56; p = 0.02), HVPG ≥ 16 mmHg (HR, 0.42; p < 0.01), or CTP class B/C (HR, 0.52; p < 0.01). Low-dose NSBB was more beneficial with 56% risk reduction (p < 0.01) of mortality compared with 33% risk reduction in the high-dose NSBB (p = 0.05).NSBB therapy was associated with longer survival in PP and SP groups who had an advanced stage of cirrhosis. Moreover, low-dose NSBB exhibited a better benefit than a standard-titrated high-dose NSBB with better tolerability.CONCLUSIONNSBB therapy was associated with longer survival in PP and SP groups who had an advanced stage of cirrhosis. Moreover, low-dose NSBB exhibited a better benefit than a standard-titrated high-dose NSBB with better tolerability.
We investigated the effect of non-selective β-blockers (NSBB) in real-world situations and whether low-dose NSBB is beneficial compared to maximally tolerated doses. We performed a retrospective study of 740 patients with cirrhosis requiring prophylactic treatment of esophageal varices: 473 primary prophylaxis (PP: NSBB = 349, non-NSBB = 124) and 267 secondary prophylaxis (SP: NSBB = 200, non-NSBB = 67). The NSBB group was divided into low-dose (≤ 80 mg/day) and high-dose (> 80 mg/day). In the PP group, NSBB treatment reduced mortality and showed the most pronounced effect in patients with moderate/severe ascites (hazard ratio [HR], 0.46; p < 0.01), HVPG ≥ 16 mmHg (HR, 0.53; p = 0.04), or CTP class B/C (HR, 0.46; p < 0.01) but not in those with no/mild ascites, HVPG < 16 mmHg, or CTP class A. Low-dose NSBB group showed a significant reduction in mortality compared with non-NSBB (moderate/severe ascites: HR, 0.61; p = 0.02 and CTP class B/C: HR, 0.41; p < 0.01) and the effect size was stronger than the high-dose NSBB. NSBB was associated with a reduced risk of infection (HR, 0.36; p = 0.01). In the SP group, NSBB prolonged survival in patients with moderate/severe ascites (HR, 0.56; p = 0.02), HVPG ≥ 16 mmHg (HR, 0.42; p < 0.01), or CTP class B/C (HR, 0.52; p < 0.01). Low-dose NSBB was more beneficial with 56% risk reduction (p < 0.01) of mortality compared with 33% risk reduction in the high-dose NSBB (p = 0.05). NSBB therapy was associated with longer survival in PP and SP groups who had an advanced stage of cirrhosis. Moreover, low-dose NSBB exhibited a better benefit than a standard-titrated high-dose NSBB with better tolerability.
Background/Aim We investigated the effect of non-selective β-blockers (NSBB) in real-world situations and whether low-dose NSBB is beneficial compared to maximally tolerated doses. Methods We performed a retrospective study of 740 patients with cirrhosis requiring prophylactic treatment of esophageal varices: 473 primary prophylaxis (PP: NSBB = 349, non-NSBB = 124) and 267 secondary prophylaxis (SP: NSBB = 200, non-NSBB = 67). The NSBB group was divided into low-dose (≤ 80 mg/day) and high-dose (> 80 mg/day). Results In the PP group, NSBB treatment reduced mortality and showed the most pronounced effect in patients with moderate/severe ascites (hazard ratio [HR], 0.46; p  < 0.01), HVPG ≥ 16 mmHg (HR, 0.53; p  = 0.04), or CTP class B/C (HR, 0.46; p  < 0.01) but not in those with no/mild ascites, HVPG < 16 mmHg, or CTP class A. Low-dose NSBB group showed a significant reduction in mortality compared with non-NSBB (moderate/severe ascites: HR, 0.61; p  = 0.02 and CTP class B/C: HR, 0.41; p  < 0.01) and the effect size was stronger than the high-dose NSBB. NSBB was associated with a reduced risk of infection (HR, 0.36; p  = 0.01). In the SP group, NSBB prolonged survival in patients with moderate/severe ascites (HR, 0.56; p  = 0.02), HVPG ≥ 16 mmHg (HR, 0.42; p  < 0.01), or CTP class B/C (HR, 0.52; p  < 0.01). Low-dose NSBB was more beneficial with 56% risk reduction ( p  < 0.01) of mortality compared with 33% risk reduction in the high-dose NSBB ( p  = 0.05). Conclusion NSBB therapy was associated with longer survival in PP and SP groups who had an advanced stage of cirrhosis. Moreover, low-dose NSBB exhibited a better benefit than a standard-titrated high-dose NSBB with better tolerability.
Author Kim, Dong Joon
Kang, Seong Hee
Lee, Minjong
Lee, Jun Hyeok
Jun, Baek Gyu
Kim, Young Don
Cheon, Gab Jin
Kim, Tae Suk
Choi, Dae Hee
Baik, Soon Koo
Kim, Moon Young
Suk, Ki Tae
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  surname: Kang
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  organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Yonsei University Wonju College of Medicine, Regenerative Medicine Research Center, Yonsei University Wonju College of Medicine, Cell Therapy and Tissue Engineering Center, Yonsei University Wonju College of Medicine
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  organization: School of Medicine, Ewha Womans University, Department of Internal Medicine, Kangwon National University Hospital
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  givenname: Moon Young
  orcidid: 0000-0002-2501-2206
  surname: Kim
  fullname: Kim, Moon Young
  email: drkimmy@yonsei.ac.kr
  organization: Division of Gastroenterology and Hepatology, Department of Internal Medicine, Yonsei University Wonju College of Medicine, Regenerative Medicine Research Center, Yonsei University Wonju College of Medicine, Cell Therapy and Tissue Engineering Center, Yonsei University Wonju College of Medicine
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  fullname: Kim, Tae Suk
  organization: Department of Internal Medicine, Kangwon National University Hospital
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  fullname: Choi, Dae Hee
  organization: Department of Internal Medicine, Kangwon National University Hospital
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  givenname: Ki Tae
  surname: Suk
  fullname: Suk, Ki Tae
  organization: Department of Internal Medicine, Hallym University College of Medicine
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  surname: Kim
  fullname: Kim, Young Don
  organization: Department of Internal Medicine, University of Ulsan College of Medicine
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Issue 2
Keywords Treatment
Portal hypertension
Hepatic venous pressure gradient
Severity
Ascites
Liver cirrhosis
Survival
Low-dose non-selective β-blockers
Nonselective β-blockers
Esophageal varix
Language English
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crossref_citationtrail_10_1007_s12072_021_10160_3
springer_journals_10_1007_s12072_021_10160_3
PublicationCentury 2000
PublicationDate 2021-04-01
PublicationDateYYYYMMDD 2021-04-01
PublicationDate_xml – month: 04
  year: 2021
  text: 2021-04-01
  day: 01
PublicationDecade 2020
PublicationPlace New Delhi
PublicationPlace_xml – name: New Delhi
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PublicationTitle Hepatology international
PublicationTitleAbbrev Hepatol Int
PublicationTitleAlternate Hepatol Int
PublicationYear 2021
Publisher Springer India
Springer Nature B.V
Publisher_xml – name: Springer India
– name: Springer Nature B.V
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Snippet Background/Aim We investigated the effect of non-selective β-blockers (NSBB) in real-world situations and whether low-dose NSBB is beneficial compared to...
We investigated the effect of non-selective β-blockers (NSBB) in real-world situations and whether low-dose NSBB is beneficial compared to maximally tolerated...
Background/AimWe investigated the effect of non-selective β-blockers (NSBB) in real-world situations and whether low-dose NSBB is beneficial compared to...
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SubjectTerms Ascites
Beta blockers
Cirrhosis
Colorectal Surgery
Disease prevention
Esophagus
Health risks
Hepatology
Hypertension
Liver cirrhosis
Medicine
Medicine & Public Health
Mortality
Original Article
Prophylaxis
Risk management
Risk reduction
Surgery
Survival
Title The longitudinal outcomes of applying non-selective beta-blockers in portal hypertension: real-world multicenter study
URI https://link.springer.com/article/10.1007/s12072-021-10160-3
https://www.ncbi.nlm.nih.gov/pubmed/33860898
https://www.proquest.com/docview/2531566170
https://www.proquest.com/docview/2514605109
Volume 15
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