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Quantitative analysis of Troponin I serum values in patients with acute cholecystitis 

Quantitative analysis of Troponin I serum values in patients with acute cholecystitis . Babic Ž, Bogdanović Z, Dorosulić Z, Basha M, Krznarić Ž, Sjekavica I, Kujundžić M, Tadić M, Banić M, Jagić V, Marušić M Coll Antropol. 2012 Mar;36(1):145-50. INTRODUCTION.

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Quantitative analysis of Troponin I serum values in patients with acute cholecystitis 

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  1. Quantitative analysis of Troponin I serum values in patients with acute cholecystitis  Babic Ž, Bogdanović Z, Dorosulić Z, Basha M, Krznarić Ž, Sjekavica I,Kujundžić M, Tadić M, Banić M, Jagić V, Marušić M Coll Antropol. 2012 Mar;36(1):145-50

  2. INTRODUCTION We studied troponin Ic (cTnI) as a new parameter, that until now, when significantly elevated has represented myocardial hypoxia and infarction]. Non-specific elevations of the cTnI (less than 0.05ug/L), is a sign of myocardial hypoxia but not infarction. Myocardial hypoxia can also result from systemic hypoxia caused by a severe form of acute cholecystitis. 

  3. PATIENTS AND METHODS MATERIALS Collected from the 65 subjects upon their written informed consents, according to the Helsinki Declaration and the Hospital Ethics Committee. In 65 patients with acute cholecystitis we measured the Troponin I (cTnI) level. Diagnose of acute cholecystitis was inclusion criteria. Acute cholecystitis was diagnosed by standard clinical, laboratory and ultrasound based signs and symptoms. We have used Tokyo Guidelines criteria for severity of acute clolecystitis (moderate, severe)

  4. PATIENTS AND METHODS • Inclusion criteria • A) Clinical symptoms • Local signs of inflammation: • upper right quadrant (RUQ) pain 1-2 hours after a meal: mass/pain/tenderness • Murphy sign • propagates towards the scapula and back in association with elevated body temperature • B) Systemic signs of inflammation • Fever • Laboratory signs: • high leukocyte count (WBC) • elevated serum C-reactive protein value

  5. PATIENTS AND METHODS • C) Immaging finding characteristic of acute inflammation • CT, MR (enlarged, thickened wall, pericholecystitic fluid, linear high density areas in pericholecystitis fat tissue, pericholecystitis high signal) • Abdominal Ulrasound signs of acute cholecystitis: • Sonographic Murphy sign • Thickhness of the gallbladder wall > 4 mm with signs of dissection (front wall) • presence of incarcerated gallstone, debris, and pericholecystic fluid • Enlarged gallbladder (>8cm long axis, >4cm short axis) • one in A+, one in B+, and C confirms A and B

  6. PATIENTS AND METHODS • Tokyo Guidelines (Criteria) • parameters that represented the local status of inflammation • systemic response to acute cholecystitis • depending on disease severity like hypoxia and circulation • Mild form • Acute cholecystitis in healthy patient with no organ dysfunction • Mild inflammatory changes in the gallbladder • Safe and Low risk of operative procedure

  7. PATIENTS AND METHODS • Tokyo Guidelines (Criteria) • Moderate form: • Accompained by any one of the following conditions • WBC>18000/mm3 • Palpable tender massin the RUQ • Duration >72h • Marked local inflammation: biliary peritonitis, pericholecystitic abscess, hepatic abscess, gangrenous cholecystitis, ephysematous cholecystitis • Difficulty to perform operative procedure

  8. PATIENTS AND METHODS • Tokyo Guidelines (Criteria) • Severe form: • Accompained by any one of the following conditions • Cardiovascular disfunction (dobutamine or dopamine >5ug/kg/min) • Neurological disfunction ( level of consciousness) • Respiratory dysfunction (PaO2/FiO3<300) • Renal dysfunction (olyguria, creatinine) • Hepatic dysfunction (PT-INR>1,5) • Hematological dysfunction (Plt>100000/mm3) • Significantly elevated WBC count • The duration of symptoms >72 h, • A palpable abdominal mass in right upper quadrant • High risk of operative procedure

  9. PATIENTS AND METHODS Exclusion criteria -Acute coronary incident -Patients with severe acute cholecystitis were tested for positive coronary artery disease by treadmill stress test (1 month later). -Patients with abnormal renal function (findings of serum and urea values) were excluded -Patients with biliary obstruction (US finding, GGT, ALP) -Patients withcomplications such as acute pancreatitis or ileus. -Upper gastrointestinal endoscopy was done to exclude all other differential diagnoses. Follow up -Up to two months after an episode of severe acute cholecystitis that was conservatively treated and healed, all patients underwent trans- abdominal or laparoscopic surgical cholecystectomy. -Gallbladder tissue sample analysis was done according to standard procedure. All patients with pathological findings that fulfilled inclusion criteria were includedin the study , while other causes of gallbladder diseases were excluded(e.g. tumor, etc.).

  10. PATIENTS AND METHODS METHODS The Troponin I measurements -The Troponin I serum values were measured by immunoflorometric method (Dimension, Dade Boehringer). We considered Troponin I values up to 0.5 ng/mL while those values between 0.5-1.5 ng/mL were excluded as a possible acute myocardial infarction. Other measurements -Ultrasound system with convex 3.5 MHz probe. -Laboratory parameters (leukocyte, CRP, amylase, bilirubin, AST, ALT, gamma glutamyl transferase, alkaline phosphatase, urea and creatinine) - measured according to standard procedures. Statistics We used software for statistical analyses that included mean, standard deviation, ANOVA, test of homogeneity of variance and multivariate multiple regression test.

  11. TABLE 1. THE MEANS AND RANGES OF PARAMETERS ACCORDING TO TOKYO CLASSIFICATION OF DISEASE SEVERITY IN PATIENTS WITH ACUTE CHOLECYSTITIS • _____________________________________________________________________________________ •   Tokyo classification score of acute cholecystitis • _____________________________________________________________________________________ •   Moderate (score=2) Severe(score=3) P • Median Range Median Range • _____________________________________________________________________________________ • Age (yrs.) 64.6 37.0 60.7 47.0 0.539 • Sex (m/f) 1.77 1.0 1.7 1.0 0.199 • Leucocytes(x109/L) 12.54 12.7 14.6 13.0 0.0284 • CRP (mg/L) 19.8 37.7 49.5 * 233.0 0.0002 • Troponin I (ug/L) 0.004 0.05 0.22 * 0.48 0.0001 • US galblder wall thicknes (mm)5.5 5.0 6.36 4.0 0.011 • US /pericholecystitis (y/n) 0.16 1.0 0.27 * 1.0 0.046 • CK (U/L ) 65.8 82.0 81.1 135.0 0.478 • Bilirubin(mol/l) 14.4 28.0 16.6 31.2 0.131 • AST (U/L) 21.1 31.0 26.4 37.0 0.451 • ALT (U/L) 21.5 34.0 23.1 34.0 0.767 • GGT (U/L) 33.3 58.0 45.1 112.0 0.171 • ALP (U/L) 71.0 80.0 67.0 85.0 0.066 • Amylase-s(U/L) 69.10 88.0 63.6 * 122.0 0.028 • Amylase-u(U/L) 131.1 200.0 143.0 264.0 0.518___________________ • Statistical significance for Troponin I was at * P <0.05 level (Levene test of Homogeeity).

  12. TABLE 2. RESULTS OF SERUM TROPONIN I VALUES IN PATIENTS WITH EITHER MODERATE OR SEVERE FORM OF ACUTE CHOLECYSTITIS • _________________________________________________________ • Moderate Severe Total • ____________________________________ • (N) (N) (N) • _________________________________________________________ • Troponin = 0 ng/mL16 12 28 • Troponin > 0 ng/mL 2 35 37 • _________________________________________________________ • 18 47 65 • _________________________________________________________ Result of 2-test presents statisticaly significant diference (P<0.005;with 2=21.26 and df=1) between the group with troponin level 0.00 ng/mL vrs. the group with troponin level higher than 0.00 ng/ml

  13. TABLE 3. TROPONIN I INMULTIPLE REGRESSION ANALYSIS WITH OTHER PARAMETERS • ________________________________________________________________________________ • US gallblader wall Troponin • Thicknes • r P r P . • _____________________________________________________________________ • Age 0.04 0.77 -0.07 0.60 • SEX 0.16 0.21 -0.10 0.44 • Leukocyte 0.14 0.26 -0.03 0.79 • CRP 0.42* 0.001 0.10 0.42 • TROPONIN 0.58* 0.001 / / • US/ Gallbladder thickness(> 6 mm) / / 0.58* 0.001 • US/pericholecystitis 0.16 0.213 0.05 0.68 • CPK -0.12 0.33 -0.03 0.81 • BIL 0.13 0.31 0.08 0.52 • AST 0.09 0.48 0.27* 0.03 • ALT 0.04 0.76 0.17 0.18 • GGT 0.22 0.079 0.26* 0.048 • ALP -0.01 0.96 -0.15 0.23 • Amylase (serm.) 0.05 0.68 0.10 0.42 • Amylase (urine) 0.08 0.53 0.10 0.41 • ______________________________________________________________________________ • Statistical significance was at * P < 0.05 leve (Multiple regresion analysis).

  14. TABLE 4. THE DIFFERENCES BETWEEN THE PARAMETERS ACORDONG TO ULTRASOUND MEASURED GALLBLADDER WALL THICKNESS IN PATIENTS WITH ACUTE CHOLECYSTITIS • ____________________________________________________________________________________________ • Gallbladder wall thickness (mm) • ____________________________________________________________________________________________ •   < 6 > 6 • xSD xSD • _____________________________________________________________________________________________ • Age (yrs.) 589 6313 0.067 • Sex (m/f) 1.660.4 1.740.4 0.257 • Leucocytes(x109/L) 144.45 143.1 0.115 • CRP (mg/L) 2211 4855 * 0.00028 • Troponin I (ug/L) 0.033 0.09 0.210.19 *0.00001 • US /pericholecystitis (y/n) 0.17 0.38 0.270.45 0.046 • CK (U/L ) 8038 7628 0.078 • Bilirubin(mol/l) 17 167 0.531 • AST (U/L) 2211 269 0.445 • ALT (U/L) 2010 239 0.657 • GGT (U/L) 3518 4422 0.368 • ALP (U/L) 6522 6922 0.678 • Amylase-s(U/L) 5821 7238 0.006 • Amylase-u(U/L) 13460 14263 0.483 • ____________________________________________________________________________________________ • Statistical significance for Troponin I was at * P <0.0001 level (Analysis of variance).

  15. CONCLUSION Taken together, the determination of Troponin I in conjunction with gallbladder wall thickness, other parameters (leukocyte count, C-reactive protein, AST, GGT etc.) and clinical presentationcould be a very sensitive, useful and simple tool, easily incorporated into daily practice. Clinically, it is very important to determine the degree of acute and non obstructive cholecystitis(mild, moderate or severe form, with or without complications). This can lead to a more precise determination of disease severity ensuring timely and appropriate therapy resulting in lower costs and fewer complications.

  16. REFERENCES: 1. KimuraY, Takada T, Kawarada Y i dr. Definitions, pathophysiology, and epidemiology of acute cholangitis and cholecystitis: Tokyo Guidelines J Hepatobiliary Pancreat Surg 2007; 14:15–26 2 2. Sekimoto M, Takada T, Kawarada Y,  i dr. Need for criteria for the diagnosis and severity assessment of acute cholangitis and cholecystitis: Tokyo Guidelines J Hepatobiliary Pancreat Surg 2007;14:11–14 3. Perry SV. Troponin I: Inhibitor or facilitator. Mol Cell Biochem 1999;190:9-32 4. Yilmaz A, Yalta K, Turgut OO, et al. Clinical importance of elevated CK-MB and troponin I levels in congestive heart failure. Adv Ther. 2006;23:1060-7 5. Babic Ž, Bogdanović Z, Dorosulić Z, Basha M, Krznarić Ž, Sjekavica I,Kujundžić M, Tadić M, Banić M, Jagić V, Marušić M. Quantitative analysis of Troponin I serum values in patients with acute cholecystitis.Coll Antropol. 2012 Mar;36(1):145-50

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