High Dose Oral Furosemide With Salt Ingestion In The Treatment Of Refractory Ascites Of Liver Cirrhosis
dc.authorscopusid | 24470317500 | |
dc.authorscopusid | 58602450200 | |
dc.authorscopusid | 56478465500 | |
dc.authorscopusid | 25641781500 | |
dc.authorscopusid | 35796175800 | |
dc.authorscopusid | 7004054394 | |
dc.contributor.author | Yakar, Tolga | |
dc.contributor.author | Demir, Mehmet | |
dc.contributor.author | Dogan, Ozlem | |
dc.contributor.author | Parlakgumus, Alper | |
dc.contributor.author | Ozer, Birol | |
dc.contributor.author | Serin, Ender | |
dc.date.accessioned | 2024-09-19T15:49:43Z | |
dc.date.available | 2024-09-19T15:49:43Z | |
dc.date.issued | 2016 | |
dc.department | Hatay Mustafa Kemal Üniversitesi | en_US |
dc.description.abstract | Purpose: We aimed to evaluate and compare the efficacy and safety of high-dose furosemide+salt orally by comparing HSS+ furosemide (i.v.) and repeated paracentesis in patients with RA. Methods: This was a prospective study of 78 cirrhotic patients with RA, randomized into three groups: Group A (n= 25) i.v. furosemide (200-300 mg bid) and 3% hypotonic saline solution (HSS) (once or twice a day); Group B (n= 26) oral furosemide tablets (360-520 mg bid) and salt (2.5 g bid); and, Group C (n= 27) repeated large-volume-paracentesis (RLVP) with albumin infusion. Patients without hyperkalemia were administrated 100 mg of spironolactone/day. During the follow-up; INR, creatinine, and total bilirubin levels were measured to determine the change in MELD (model of end stage liver disease) score. Results: Hepatic encephalopathy (HE), severe episodes of spontaneous bacterial peritonitis (SBP) and pleural effusions (PE) occurred more frequently in Group C. Improvement in Child-Pugh and MELD score was better in Group A and B than Group C. In Group B, improvements were seen in the Child-Pugh and MELD score, reduction in body weight, duration and number of hospitalization. In Groups A and B, remarkable increases in diuresis were observed (706±116 to 2425±633 mL and 691±111 to 2405±772 mL) and serum sodium levels also improved. HE and SBP were occurred more often in group C (p<0.002). Hospitalization decreased significantly in Group B (p<0.001). There was no significant difference in survival among groups. Conclusion: High dose oral furosemide with salt ingestion may be an alternative, effective, safe and well-tolerated method of therapy for RA © 2016. Clinical and Investigative Medicine. All Rights Reserved. | en_US |
dc.identifier.doi | 10.25011/CIM.V39I6.27502 | |
dc.identifier.endpage | 60 | en_US |
dc.identifier.issn | 0147-958X | |
dc.identifier.issue | 6 | en_US |
dc.identifier.pmid | 27917793 | en_US |
dc.identifier.scopus | 2-s2.0-85047594085 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 52 | en_US |
dc.identifier.uri | https://doi.org/10.25011/CIM.V39I6.27502 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12483/15356 | |
dc.identifier.volume | 39 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | The Canadian Society for Clinical Investigation | en_US |
dc.relation.ispartof | Clinical and Investigative Medicine | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Administration, Oral | en_US |
dc.subject | Adult | en_US |
dc.subject | Aged | en_US |
dc.subject | Aged, 80 and over | en_US |
dc.subject | Albumins | en_US |
dc.subject | Ascites | en_US |
dc.subject | Bilirubin | en_US |
dc.subject | Creatinine | en_US |
dc.subject | End Stage Liver Disease | en_US |
dc.subject | Female | en_US |
dc.subject | Furosemide | en_US |
dc.subject | Hepatic Encephalopathy | en_US |
dc.subject | Hospitalization | en_US |
dc.subject | Humans | en_US |
dc.subject | Hyperkalemia | en_US |
dc.subject | International Normalized Ratio | en_US |
dc.subject | Liver Cirrhosis | en_US |
dc.subject | Male | en_US |
dc.subject | Middle Aged | en_US |
dc.subject | Paracentesis | en_US |
dc.subject | Peritonitis | en_US |
dc.subject | Pleural Effusion | en_US |
dc.subject | Prospective Studies | en_US |
dc.subject | Sodium Chloride | en_US |
dc.subject | Sodium Potassium Chloride Symporter Inhibitors | en_US |
dc.subject | Spironolactone | en_US |
dc.subject | Treatment Outcome | en_US |
dc.subject | albuminoid | en_US |
dc.subject | bilirubin | en_US |
dc.subject | creatinine | en_US |
dc.subject | furosemide | en_US |
dc.subject | loop diuretic agent | en_US |
dc.subject | sodium chloride | en_US |
dc.subject | spironolactone | en_US |
dc.subject | adult | en_US |
dc.subject | aged | en_US |
dc.subject | ascites | en_US |
dc.subject | blood | en_US |
dc.subject | chemically induced | en_US |
dc.subject | chemistry | en_US |
dc.subject | complication | en_US |
dc.subject | controlled study | en_US |
dc.subject | end stage liver disease | en_US |
dc.subject | female | en_US |
dc.subject | hepatic encephalopathy | en_US |
dc.subject | hospitalization | en_US |
dc.subject | human | en_US |
dc.subject | hyperkalemia | en_US |
dc.subject | international normalized ratio | en_US |
dc.subject | liver cirrhosis | en_US |
dc.subject | male | en_US |
dc.subject | microbiology | en_US |
dc.subject | middle aged | en_US |
dc.subject | oral drug administration | en_US |
dc.subject | paracentesis | en_US |
dc.subject | peritonitis | en_US |
dc.subject | pleura effusion | en_US |
dc.subject | prospective study | en_US |
dc.subject | randomized controlled trial | en_US |
dc.subject | treatment outcome | en_US |
dc.subject | very elderly | en_US |
dc.title | High Dose Oral Furosemide With Salt Ingestion In The Treatment Of Refractory Ascites Of Liver Cirrhosis | en_US |
dc.type | Article | en_US |