Primary biliary cirrhosis: 12-year experience of observation

Aim. To ascertain initial signs of primary biliary cirrhosis (PBC), criteria of its early diagnosis, variants of the course, clinical picture and life quality of PBC patients. Material and methods. 128 PBC patients were examined in the Central Research Institute of Gastroenterology from 1991 to 2002...

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Main Authors: E V Golovanova, L Yu Ilchenko, Т М Tsaregorodtseva, T I Serova, R В Gudkova, S D Shepeleva, V D Tkachev
Format: Article
Language:Russian
Published: "Consilium Medicum" Publishing house 2003-02-01
Series:Терапевтический архив
Subjects:
Online Access:https://ter-arkhiv.ru/0040-3660/article/view/29308
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spelling doaj-c0e5b1c8c38e4262b9a43080f99253692020-11-25T02:38:47Zrus"Consilium Medicum" Publishing houseТерапевтический архив0040-36602309-53422003-02-01782263026344Primary biliary cirrhosis: 12-year experience of observationE V GolovanovaL Yu IlchenkoТ М TsaregorodtsevaT I SerovaR В GudkovaS D ShepelevaV D TkachevAim. To ascertain initial signs of primary biliary cirrhosis (PBC), criteria of its early diagnosis, variants of the course, clinical picture and life quality of PBC patients. Material and methods. 128 PBC patients were examined in the Central Research Institute of Gastroenterology from 1991 to 2002. Quality of life was assessed by SF-36 questionnaire adapted for patients with chronic cholestatic diseases of the liver. Results. The patients complained of skin pruritus (80%), jaundice (66%), fatigue (68.8%), weight loss (24.6%o). The disease manifested with skin pruritis in 75.8%, jaundice - in 12.5% patients. Decompensated hepatic cirrhosis (Child-Pugh C) at first hospitalisation was diagnosed in 11.7% cases. The earlest and most significant biochemical markers of PBS were high activity of gammaglutamiltranspeptidase (GGTP) and alkaline phosphatase (AP). IgM level was high in 70.5% cases. Anfimitochondrial antibodies were detected in 83.6% examinees. Overlapping with autoimmune hepatitis was seen in 9.4%. One-third of the patients had systemic symptoms. Quality of life deteriorated. Conclusion. PBC may be long asymptomatic. The absence of skin pruritus is not a sure sign of the disease absence. To detect PBC early, young and middle-aged women with unexplained weakness or skin pruritus should undergo a comprehensive examination including measurements of GGTP, AP, AM A, IgM, morphological investigation of liver tissue. PBC patients had low quality of life. This should be accounted for when treating patients, in determination of their working ability and for early referral for liver transplantation.https://ter-arkhiv.ru/0040-3660/article/view/29308primary biliary cirrhosisantimitochondrial antibodiesquality of life
collection DOAJ
language Russian
format Article
sources DOAJ
author E V Golovanova
L Yu Ilchenko
Т М Tsaregorodtseva
T I Serova
R В Gudkova
S D Shepeleva
V D Tkachev
spellingShingle E V Golovanova
L Yu Ilchenko
Т М Tsaregorodtseva
T I Serova
R В Gudkova
S D Shepeleva
V D Tkachev
Primary biliary cirrhosis: 12-year experience of observation
Терапевтический архив
primary biliary cirrhosis
antimitochondrial antibodies
quality of life
author_facet E V Golovanova
L Yu Ilchenko
Т М Tsaregorodtseva
T I Serova
R В Gudkova
S D Shepeleva
V D Tkachev
author_sort E V Golovanova
title Primary biliary cirrhosis: 12-year experience of observation
title_short Primary biliary cirrhosis: 12-year experience of observation
title_full Primary biliary cirrhosis: 12-year experience of observation
title_fullStr Primary biliary cirrhosis: 12-year experience of observation
title_full_unstemmed Primary biliary cirrhosis: 12-year experience of observation
title_sort primary biliary cirrhosis: 12-year experience of observation
publisher "Consilium Medicum" Publishing house
series Терапевтический архив
issn 0040-3660
2309-5342
publishDate 2003-02-01
description Aim. To ascertain initial signs of primary biliary cirrhosis (PBC), criteria of its early diagnosis, variants of the course, clinical picture and life quality of PBC patients. Material and methods. 128 PBC patients were examined in the Central Research Institute of Gastroenterology from 1991 to 2002. Quality of life was assessed by SF-36 questionnaire adapted for patients with chronic cholestatic diseases of the liver. Results. The patients complained of skin pruritus (80%), jaundice (66%), fatigue (68.8%), weight loss (24.6%o). The disease manifested with skin pruritis in 75.8%, jaundice - in 12.5% patients. Decompensated hepatic cirrhosis (Child-Pugh C) at first hospitalisation was diagnosed in 11.7% cases. The earlest and most significant biochemical markers of PBS were high activity of gammaglutamiltranspeptidase (GGTP) and alkaline phosphatase (AP). IgM level was high in 70.5% cases. Anfimitochondrial antibodies were detected in 83.6% examinees. Overlapping with autoimmune hepatitis was seen in 9.4%. One-third of the patients had systemic symptoms. Quality of life deteriorated. Conclusion. PBC may be long asymptomatic. The absence of skin pruritus is not a sure sign of the disease absence. To detect PBC early, young and middle-aged women with unexplained weakness or skin pruritus should undergo a comprehensive examination including measurements of GGTP, AP, AM A, IgM, morphological investigation of liver tissue. PBC patients had low quality of life. This should be accounted for when treating patients, in determination of their working ability and for early referral for liver transplantation.
topic primary biliary cirrhosis
antimitochondrial antibodies
quality of life
url https://ter-arkhiv.ru/0040-3660/article/view/29308
work_keys_str_mv AT evgolovanova primarybiliarycirrhosis12yearexperienceofobservation
AT lyuilchenko primarybiliarycirrhosis12yearexperienceofobservation
AT tmtsaregorodtseva primarybiliarycirrhosis12yearexperienceofobservation
AT tiserova primarybiliarycirrhosis12yearexperienceofobservation
AT rvgudkova primarybiliarycirrhosis12yearexperienceofobservation
AT sdshepeleva primarybiliarycirrhosis12yearexperienceofobservation
AT vdtkachev primarybiliarycirrhosis12yearexperienceofobservation
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