Human Kidney Histopathology in Obstructive Jaundice

Patients With Obstructive Jaundice Clinical Trial

Official title:

Phase 4 Study :Human Kidney Histopathology in Acute Obstructive Jaundice: a Prospective Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01090193
• Other study ID #: BZYK01
• Status: Completed
• Phase: Phase 4
• First received: March 18, 2010
• Last updated: March 18, 2010
• Start date: January 2009
• Est. completion date: March 2010

Study information

• Verified date: January 2009
• Source: Turkish Ministry of Health Izmir Teaching Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Turkey: Ethics CommitteeTurkey: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

Introduction: Cholemia and bacterial translocation with portal endotoxemia are integral in the pathogenesis of obstructive jaundice (OJ). There is sufficient experimental data about hemodynamic and histopathologic consequences of OJ. On the contrary, pathologic information of renal changes in patients with OJ is still lacking. Therefore; the primary objective of this prospective study is to demonstrate the specific histopathologic changes in kidneys of patients with short-term biliary tract obstruction receiving a standard perioperative medical treatment protocol.

Description:

Twenty consecutive patients with biliary obstruction were included. Fluid replacement, prevention of biliary sepsis and portal endotoxemia were mainstays of the perioperative treatment protocol. Fluid and electrolyte balance was maintained by twice daily body weight calculations, central venous pressure and mean arterial pressure (MAP) monitoring . Renal function was assessed by glomerular filtration rate estimation via MDRD-7 formula.

Kidney biopsy evaluation was focused on tubular changes, thrombotic microangiopathy, endothelial damage and peritubular capillary (PTC) dilatation with or without C4d staining. Fresh frozen sections were evaluated with immunoflourescence (IF)microscopy for glomerular IgG, IgA, IgM, C3, and C1q staining.

Despite those favourable figures, dilatation of peritubular venules and acute tubular necrosis were demonstrated synchronously in all cases. C4d staining in PTC and arterioles and thrombotic microangiopathy were entirely absent in the study group. Immune complex deposits in peritubular capillaries and in glomeruli were not detected. Three patients had isolated glomerular C4d deposition without accompanying thrombotic microangiopathy and IgG, IgA, IgM, C3, and C1q staining of glomerular capillaries in IF microscopy.

Discussion: This study is the first in the literature to address the histopathologic changes that occur in humans with short-term biliary obstruction. ATN and venous dilatation was observed in all biopsies, without exception, despite the maintenance of strict volume control in all patients. The adequacy of volume control may not be implicated in those results; rather a possible mechanism related to untrapped endotoxin in the gut lumen or systemic circulation might lead to prolonged peritubular capillary dilatation and hypoperfusion with synchronous acute tubular necrosis . Absolute recovery of renal function in all patients and the demonstration of solitary ATN with no microvascular-glomerular-interstitial inflammation or injury, suggests that the perioperative treatment regime in this study is fairly efficacious in short-term OJ.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: March 2010
• Est. primary completion date: March 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 26 Years to 86 Years

Eligibility

Inclusion Criteria:

• Between January 2009 and January 2010, twenty consecutive patients with an equal distribution of biliary obstruction type (10 malignant and 10 benign) were included into the study.

Exclusion Criteria:

• Patients over 60 years of age or those with a history of co-morbid cardiac disease were initially evaluated by echocardiography.

• Those with an ejection fraction rate <50% and left ventricular end-diastolic diameter (LVDD) over 52 mm. were excluded from the study because of the already existing left ventricular dysfunction compromising the optimisation of fluid replacement.

• Patients with a history and serologic evidence of acute/chronic parenchymal kidney or liver disease were also excluded.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Jaundice
• Jaundice, Obstructive
• Patients With Obstructive Jaundice

Intervention

Procedure:
• Whipple operation,Hepaticojejunostomy
Whipple operation, Hepaticojejunostomy

Locations

Country	Name	City	State
Turkey	Izmir Teaching Hospital, Department of General Surgery	Izmir

Sponsors (1)

Lead Sponsor	Collaborator
Turkish Ministry of Health Izmir Teaching Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Green J, Better OS. Systemic hypotension and renal failure in obstructive jaundice-mechanistic and therapeutic aspects. J Am Soc Nephrol. 1995 May;5(11):1853-71. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Human kidney histopathology in acute obstructive jaundice: a prospective study	the primary objective of this prospective study is to demonstrate the specific histopathologic changes in kidney parenchyme of patients undergoing surgery for short-term biliary tract obstruction.	12 months	Yes
Secondary	Human kidney histopathology in acute obstructive jaundice: a prospective study	The secondary objective is to approve the feasibility of a standard perioperative medical treatment protocol, which has been implemented on a routine basis in our department over the last decade.	12 months	Yes

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