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Pemeriksaan Fungsi Hati dr.Diah Puspita Rini, SpPK Liver 1. Biochemycal hepatocyte system: - protein & lipoprotein synthesis - aerob/anaerob metabolism glucose - glycogen synthesis & breakdown - iron & vitamin storage, drug metabolism - synthesis & clearance of hormone 2. Hepatobiliary system: - bilirubin metabolism 3. Reticuloendothelial system: - Kupffer cells FUNCTIONS OF THE LIVER • Regulating blood glucose level by making glycogen, which is stored in hepatocytes. • Synthesizing blood glucose from amino acids of lactate through gluconeogenesis. • Converting ammonia produced from gluconeogenetic by-products and bacteria to urea • Synthesizing plasma proteins such as albumin, globulins, clotting factors, and lipoproteins. • Breaking down fatty acids into ketone bodies • Storing vitamins and trace metals • Affecting drug metabolism and detoxification • Secreting bile Manfaat Tes Fungsi Hati 1. Deteksi penyebab - gangguan fungsi hati - penyakit hati 2. Derajat gangguan fungsi/penyakit hati 3. Evaluasi : Perjalanan Penyakit Hasil terapi Prognosis Keterbatasan TFH 1. Fungsi metabolik hati beragam 2. Kapasitas cadangan fungsi hati besar 3. Korelasi dg derajat kerusakan hati tidak linier 4. Sensitivitas thd kerusakan jar hati tidak sama 5. Spesifisitas tidak sama → tdk ada tes tunggal yg dpt mendeteksi seluruh penyakit hati Macam Tes Fungsi hati 1. Tes mengetahui gangguan fungsi “Uptake” : bilirubin konjugasi : bilirubin ekskresi : bilirubin, asam empedu sintesis : albumin faktor koagulasi kolinesterase 2. Tes integritas sel : AST, ALT, LDH 3. Tes kolestasis : Bilirubin, ALP, γ GT, 5’NT 4. Tes etiologi – Marker hepatitis – Tumor marker : CEA, AFP BILIRUBIN - Unconjugated bilirubin : Not water soluble Toxic to cells –Bound to albumin making it soluble in plasma –Transported through plasma to liver for excretion Conjugated bilirubin : 1. Water soluble 2. Less toxic to cells 3. Can pass glomerular filtering membrane Not found in plasma unless •Liver cell injury •Obstruction Then will be found in urine •Bilirubin dipstick: (+) Gangguan Metabolisme Bilirubin • Icterus/Jaundice: keadaan yang disebabkan peningkatan bilirubin plasma – Pre hepatik: anemia hemolitik – Hepatik: kerusakan hepatoselular – Post hepatik: batu empedu, tumor pankreas • Klinis : bila bilirubin total > 2.5mg/dl ICTERUS (JAUNDICE) bila bilirubin unconjugated > 15 mg/dl KERN ICTERUS (terutama pada bayi) Gangguan metabolisme bilirubin 3 2 1 10 10 Peningkatan Unconjugated Bilirubin 1.Peningkatan produksi: Hemolisis 2.Gangguan uptake : sindroma Gilbert’s 3. Gangguan konjugasi : - Neonatal jaundice enzim glukuronil-transferase belum aktif - penyakit hati yang berat (hepatitis, sepsis) - beberapa macam obat : *kloramfenikol *pregnanediol breast-milk jaundice - defisiensi glukuronil transferase herediter sindroma Criggler Najjar Peningkatan Conjugated Bilirubin • • • • Kolestasis intra dan ekstra hepatik Hepatitis, sirosis hepatis Atresia bilier Kelainan kongenital, ggn ekskresi: - Sindroma ROTOR - Sindroma DUBIN-JOHNSON Ciri Klinis Hemolitik Hepatoseluler Obstruktif Warna kulit Kuning pucat Kuning muda-tua kuning Warna urine normal Gelap Gelap Warna feses Normal/gelap Pucat (sterkobilin ↓) Warna ≈ dempul Pruritus - - Menetap Bilirubin indirek ↑ ↑ ↑ Bilirubin direk N ↑ ↑ Bilirubin urine - ↑ ↑ Urobilinogen urine ↑ Sedikit meningkat ↓ Analisis Laboratorium Bilirubin Nilai yang akurat tergantung dari pengambilan dan penanganan spesimen yang benar Sampel tidak hemolisis (hasil akan rendah palsu karena adanya interference) Tidak lipemia (lebih utama sampel dalam keadaan puasa) Light sensitive (cahaya merusak bilirubin) • BilirubinTotal : diukur dari kedua macam bilirubin (unconjugated and conjugated) • Bilirubin Direct : hanya mengukur conjugated bilirubin • Parameter dihitung : Total – direct = unconjugated (indirect) Expected Values: Adults •Total bilirubin: 0.2 – 1.0 mg/dl •Conjugated bilirubin: 0.0 - 0.2 mg/dl •Unconjugated bilirubin: 0.2 – 0.8 mg/dl •Urine bilirubin: negative Expected Values: Infants Total bilirubin Premature Full Term 24 hours 1 – 6 mg/dl 2 – 6 mg/dl 48 hours 6 – 8 mg/dl 6 – 7 mg/dl 3-5 days 10 – 12 mg/dl 4 – 6 mg/dl FUNGSI SINTESIS HATI • Sintesis – Total protein – Albumin – Protein koagulasi /faktor koagulasi • Banyak disintesis di hati • Membutuhkan vitamin K untuk sintesisnya – Cholinesterase Perubahan Fraksi Protein Pada Penyakit Hati ALBUMIN ↓ Kapasitas cadangan sintesis protein besar, bila Albumin berarti KERUSAKAN HEPATOSIT LUAS/BERAT Waktu Paruh albumin : cukup lama ( 20 hr ) bila albumin → kerusakan hepatosit berlangsung lama GLOBULIN ↑ terutama globulin - respon terhadap inflamasi - kompensasi FAKTOR KOAGULASI PLASMA disintesis oleh hepatosit - kecuali faktor III,IV,VIII penyakit hati diffus gangguan sintesis faktor koagulasi. sintesis faktor II, VII, IX & X (prothrombin complex) perlu vit K. test : PPT 19 19 Protein disintesis di hati Sintesis membutuhkan vit.K Dipengaruhi oleh : - peny.hepatoselular (ggn sintesis) - peny. Obstruktif (ggn absorpsi vit.K) CHOLINESTERASE (CHE) - Penyakit hati kronis, sirosis, hepatitis akut fulminan. - Malnutrisi. - Keracunan insektisida (organofosfat) AKTIVITAS , SINTESIS NORMAL Pada hepatitis akut CHE prognosis buruk. ENZIM • Protein intraseluler yang dikeluarkan ke dalam sirkulasi krn adanya kematian /injury sel • • • • • Cardiac enzymes (CK, CK-MB, LD, AST) → IMA Pancreatic enzymes (amylase, lipase) → pankreatitis Muscle enzymes (CK, LD, AST) → muscular dystrophy Bone (ALP) → peny. degeneratif tulang Liver enzymes (AST, ALT, ALP, GGT)→ peny. liver • Fungsi: katalisator LOKASI ENZIM DALAM HEPATOSIT Hepatocyte with cell organelles (schematic representation) and localization of the diagnostically most important enzymes etc AST,ALT,LDH ALP GGT 1. Stellate Kupffer cell 2. Space of Disse 3. Granular endopl. retic:ChE 4. Smooth endopl. retic 5. Mitochondrion: GlDH,AST 6. Bile canaliculi:ALP,LAP,G-GT 7. Nucleus 8. Lysosomes :hydrolases 9. Cytoplasm:LDH,ALAT,AST Iron AST ChE 23 23 TRANSAMINASE SERUM SGOT : Serum Glutamic Oxaloacetic Transaminase/ AST : ASpartate amino Transferase → liver, heart skeletal muscle, kidneys, brain, RBCs half-life 17hrs In liver 20% activity is cytosolic and 80% mitochondrial SGPT : Serum Glutamic Pyruvic Transaminase/ ALT : ALanine amino Transferase - more specific to liver, very low concentrations in kidney and skeletal muscles. In liver totally cytosolic Half-life 47hrs 24 AST dan ALT • Dalam sitoplasma hepatosit: - kadar AST 1,5 – 2 x ALT • Pada hepatitis akut: – AST > ALT – 24-48 jam: kerusakan berlanjut → ALT > AST krn waktu paruh yg lebih panjang • Kerusakan hati ringan: ALT ↑ • Kerusakan hati berat/nekrosis : AST ↑ 25 25 Medications causing elevation of aminotransferases Acetaminophen Amoxicillin-clavulanic acid HMGCoA reductase inhbtrs Herbs and toxins INH •Herbs/alt. medicines NSAIDS •Illicit drugs Phenytoin •Toxins Valproate Many others RASIO AST/ALT ( de RITIS ) Biasa dipakai bila ada kenaikan transaminase tidak terlalu tinggi <1 >1 KERUSAKAN HATI AKUT KERUSAKAN HATI MENAHUN / SIROSIS • DASAR : ALT KERUSAKAN MEMBRAN. AST KERUSAKAN ORGANEL + KERUSAKAN MEMBRAN 27 27 RASIO AST/ALT ( rasio de RITIS ) Biasanya tidak banyak berarti, kecuali bila: - rasio > 2 : 1 → alkoholic liver disease - sirosis / hipertensi portal + rasio > 3: primary billiary cirrhosis - ALT > AST : - viral hepatitis - chronic active hepatitis - cholestasis 28 28 ALP (Alkaline Phosphatase) • Dapat ditemukan: • Liver • Tulang • Ginjal • Intestine • Placenta • ALP liver: • Half life 3 hari • Permukaan kanalikuli → disfungsi bilier, ↑ 10x N LDH • Terdapat di hampir semua sel • LD isoenzim menunjukkan spesifisitas jaringan LD-1 (HHHH) LD-2 (HHHM) Cardiac muscle, kidney, erythrocyte Infark (± 72 jam) Peny. Hemolitik Sampel lisis LD-4 (HMMM) LD-5 (MMMM) Liver, skeletal muscle Peny. Liver Skeletal muscle disease Gamma-GT • hepatocytes and biliary epithelial cells, pancreas, renal tubules and intestine • Very sensitive but Non-specific • Raised in ANY liver discease hepatocellular or cholestatic • Usefulness limited • Confirm hepatic source for a raised ALP • Alcohol • Isolated increase does not require any further evaluation, suggest watch and repeat only if other LFT’s become abnormal then investigate Causes of raised serum gammaglutamyl transferase (GGT) INTERPRETASI TFH • Markers of Hepatocellular (Transaminases) : - AST - ALT • Markers of Cholestasis: • ALP • Gamma GT • 5’ nucleotidase / 5’NT damage 34 34 • Bilirubin, Albumin dan Prothrombin time (INR) – Useful indicators of liver synthetic function – In primary care when associated with liver disease abnormalities should raise concern – Thrombocytopaenia is a sensitive indicator of liver fibrosis Disorder Bilirubin AST/ ALT ALP Albumin PT Hemolysis / Gilberts unconj ↑ N N N N Acute hep. cellular ds Both elevate Bilirubin uria+ Elevate ALT > AST N/<3 times N N Usually N Chronic hep. cellular. ds Both elevate Bilirubin uria+ Elevate <300u/l N/ <3 times N Decrease prolonged Disorder Bilirubin AST/ ALT ALP Albumin PT ↓ prolonged Alcohol hepatitis cirrhosis Both elevate >2 sugg bilirubinuria + >3 diag N / <3 times N Obs. jaundice Both elevate N to mod Bilirubinuria+ elevate Elevate >4 times N N unless chronic N/ Prolonged Elevate >4 times GGT,5’N N N Infiltrative disease N N / slight elevate SIROSIS HATI Definisi: Penyakit hati yang kronik dan progresif mengakibatkan destruksi dan degenerasi sel parenkim yang extensif Terdiri dari 4 tipe: Alcoholic (Laennec’s) cirrhosis → Associated with alcohol abuse Postnecrotic cirrhosis → Complication of toxic or viral hepatitis Biliary cirrhosis → Associated with chronic biliary obstruction and infection Cardiac cirrhosis → Results from longstanding severe right-sided heart failure Manifestations of Liver Cirrhosis Fig. 42-5 SIROSIS HATI COMPENSATED PHASE : - Gangguan fungsi minimal ACTIVE PHASE : - Nekrosis progresif ( ALT ) - Fibrosis kolestasis ( ALP , BILI ) DECOMPENSATED PHASE : - Gangguan fungsi berat + hipo albumin + hiperbilirubinemia GAGAL HATI 40 40 SOAL KASUS • Laki-laki 48 th datang dengan keluhan nyeri perut kanan atas dan febris naik turun selama 3 bulan. Nafsu makan dan BB↓. Dia menderita hepatitis 10 thn y.l. Pemeriksaan fisik: sklera ikterik, hepatomegali 2 cm bac, splenomegali (+) • Hasil Lab: Hb 9 g /dL WBC 8000/uL PLT 90.000/uL ALT 120 U/L (normal < 45) AST 200 U/L (normal < 45) Bilirubin total 10 mg/dl (normal 0,3-1 mg/dl) Bilirubin direk 7,8 mg/dl (normal 0-0,3 mg/dl) HBsAg (+), HBeAg (+), anti-HBc IgM (+) a. Apa diagnosis pasien ini? b. Ikterus tipe apa yang dialami oleh pasien sehingga terjadi peningkatan bilirubin? Need a break?? 44