FIELD: medicine.
SUBSTANCE: clinical and physiological examinations are done on a patient, as well as determination and quantitative grading of subsequent evaluation criteria, which include determination of somatic protein deficiency, determination of visceral protein deficiency from the level of serum albumin, determination of ascite intensity, determination of neurologic status, evaluation of central hemodynamics and determination of presence of jaundice from the level of bilirubin. Functional class is then determined from groups and transition groups A, A-B, B, B-C, C, to which the patient relates on presence of more than 3 parametres, corresponding to any given functional class, where group A is characterised by the following parametres: somatic protein deficiency 0-5%, visceral protein deficiency from the level of serum albumin >40, absence of ascite from USD data, neurologic status - absence of clinical and EEG encephalopathy features, central hemodynamic state - normal parametres, absence jaundice from the level of bilirubin, where functional class of this group characterises compensation stage of chronic hepatocellular impairment. Group A-B is characterised by the following parametres: somatic protein deficiency 5-10%, visceral protein deficiency from the level of serum albumin 40-35, absence of ascite from USD data, neurologic status - absence of clinical and EEG encephalopathy features, central hemodynamic state - normokinetic, increase in total peripheral resistance, presence of transient jaundice from the level of bilirubin, where functional class of this group characterises stage of relative compensation of chronic hepatocellular impairment. Group B is characterised by the following parametres: somatic protein deficiency 10-15%, visceral protein deficiency from the level of serum albumin 35-30, presence of ascite percussion in inclined places, neurologic status - presence of astenisation, central hemodynamic state - hyperkinetic, increase in circulating blood volume, more than 60 ml carbohydrates, presence of light jaundice from bilirubinemia, consisting of 1.5-2 doses, where functional class of this group characterises a stage of subcompensated chronic hepatocellular impairment. Group B-C is characterised by the following parametres: somatic protein deficiency 15-20%, visceral protein deficiency from the level of serum albumin 30-25, presence of moderate ascite - 1 stage of abdominal cavity, neurologic status - presence of latent encephalopathy, central hemodynamic state - normo-hypokinetic, positive sample volumes, 60-40 ml carbohydrates, mild jaundice from bilirubinemia, consisting of 3 doses, where functional class of this group characterises a stage of relative or early decompensation. Group C is characterised by the following parametres: somatic protein deficiency over 20%, visceral protein deficiency from the level of serum albumin less than 25, presence of intense ascite of 2 stages of abdominal cavity and more, neurologic status - acute encephalopathy of 1-2 degree, central hemodynamic state - reduction of all hemodynamic parametres, less than 40 ml carbohydrates, presence of severe jaundice from bilirubinemia consisting of more than 3 doses, where functional class of this group characterises stage of complete decompensation of chronic hepatocellular impairment.
EFFECT: increased accuracy of diagnosing liver diseases, accuracy of predicting course of a disease and extent of surgery.
3 tbl, 1 dwg
Title | Year | Author | Number |
---|---|---|---|
BIOTRANSPLANT, TREATMENT METHOD OF CHRONIC LIVER DISEASES AND TREATMENT METHOD OF LIVER CIRRHOSIS AND PORTAL HYPERTENSION | 2007 |
|
RU2368384C2 |
METHOD FOR SEVERITY DIAGNOSIS OF LIVER CIRRHOSIS OF MIXED ETIOLOGY | 2016 |
|
RU2632101C1 |
CHILD-PUGH METHOD FOR DIAGNOSTICS OF C CLASS LIVER CIRRHOSIS OF ALCOHOL GENESIS | 2016 |
|
RU2618415C1 |
METHOD FOR MIXED (HCV+ALCOHOL) ETIOLOGY LIVER CIRRHOSIS FORMATION FORECASTING | 2016 |
|
RU2618418C1 |
DIAGNOSTIC TECHNIQUE FOR SEVERITY OF VIRAL AND ALCOHOLIC CIRRHOSIS | 2010 |
|
RU2430682C1 |
METHOD OF NONINVASIVE ESTIMATION OF FUNCTIONING LIVER PULP DIMENSION IN PATIENTS WITH CIRRHOSIS AND PORTAL HYPERTENSION | 2008 |
|
RU2406445C2 |
METHOD OF DETERMINING DEGREE OF SEVERITY OF TISSUE HYPOXIA IN CHRONIC DIFFUSE HEPATIC DISEASE | 2011 |
|
RU2463611C1 |
METHOD FOR PREDICTION OF FATAL OUTCOMES IN PATIENTS SUFFERING VIRAL OR ALCOHOLIC CIRRHOSIS | 2011 |
|
RU2465818C1 |
DIAGNOSIS METHOD FOR LIVER CIRRHOSIS CLASS | 2021 |
|
RU2766768C1 |
METHOD OF PREDICTING AN INCREASED RISK OF DECOMPENSATION OF LIVER CIRRHOSIS OR THE DEVELOPMENT OF HEPATOCELLULAR CARCINOMA IN PATIENTS WITH LIVER CIRRHOSIS IN THE OUTCOME OF CHRONIC HEPATITIS C AFTER ACHIEVING A SUSTAINED VIROLOGIC RESPONSE | 2022 |
|
RU2800251C1 |
Authors
Dates
2009-08-10—Published
2007-12-26—Filed