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1.
Transplant Proc ; 40(6): 1916-7, 2008.
Article in English | MEDLINE | ID: mdl-18675088

ABSTRACT

BACKGROUND: Up to 15% of liver transplant candidates have asymptomatic coronary artery diseases, which increase the risk of cardiac complications during and after transplantation. The aim of this study was to prospectively investigate the usefulness of an integrated cardiological approach in cirrhotic patients undergoing liver transplantation. METHODS: Twenty-four consecutive patients undergoing evaluation for liver transplantation were studied by assessing risk factors for coronary artery diseases, electrocardiogram with QTc interval determination, chest X-ray, echocardiography, 24-hour Holter monitor, myocardial perfusion scintigraphy (99mTc)MIBI-GSPECT at rest and after dipyridamole infusion. Cardiac (123)I-metaiodobenzylguanidine (MIBG) scan and coronarography were performed in patients with myocardial perfusion defects. Twenty three of 24 patients underwent successful liver transplantation; one patient died on the waiting list. RESULTS: Before liver transplantation, 29% of patients were diabetic and 41% were smokers. Eleven of 24 patients had a prolonged QTc interval, and 3/24 had positive myocardioscintigraphy after dipyridamole infusion: in two coronarography was negative, while the (123)I-MIBG washout was altered. No cardiac events were recorded during the short-and long-term follow-up after surgery. CONCLUSIONS: Predictive value of positive cardiac (99mTc)MIBI-GSPECT in patients with liver cirrhosis is low, and this may be due to alterations of cardiac microvascular tone as showed by cardiac (123)I-MIBG scan.


Subject(s)
Coronary Disease/complications , Heart/diagnostic imaging , Liver Cirrhosis/complications , Liver Cirrhosis/surgery , Liver Transplantation , Adult , Coronary Disease/etiology , Electrocardiography , False Positive Reactions , Female , Follow-Up Studies , Humans , Liver Transplantation/diagnostic imaging , Male , Middle Aged , Radionuclide Imaging , Technetium Tc 99m Sestamibi , Ultrasonography
4.
Dig Dis Sci ; 42(8): 1708-14, 1997 Aug.
Article in English | MEDLINE | ID: mdl-9286238

ABSTRACT

We compared the efficacy and safety of apheresis and reinfusion of concentrated ascites (ARCA) versus total paracentesis plus intravenous albumin (PARA) in a prospective trial on cirrhotic patients with tense ascites. Twenty-four patients were randomized to either ARCA (N = 12) or PARA (N = 12), and followed for two years. Sex, age, Child's class, and renal and liver function were similar in the two groups. The times the procedures were 2.7 +/- 1.0 (ARCA) vs 2.2 +/- 1.1 (PARA) hr, with removal of 8.8 +/- 3.5 (ARCA) and 6.9 +/- 3.4 (PARA) liters of ascites and intravenous infusion of 59.8 +/- 35.2 (ARCA) and 42.5 +/- 20.5 (PARA) g of albumin. Both procedures were safe. Biochemical signs of coagulative disturbances having no clinical relevance were observed after ARCA, with an increase in prothrombin time (P = 0.005) and serum FSP (P = 0.02). No significant changes in renal function, serum albumin, or plasma and urinary electrocytes were shown. Plasma renin activity increased after PARA (P = 0.02) and plasma atrial natriuretic factor increased after ARCA (P = 0.008), although no differences were observed in diuresis in the immediate follow-up. During the long-term follow-up, patient survival and recurrence of tense ascites were the same in both groups. We conclude that apheresis and reinfusion of concentrated ascites are as safe and effective as total paracentesis with albumin infusion for the treatment of tense ascites in cirrhotic patients.


Subject(s)
Ascites/therapy , Ascitic Fluid , Liver Cirrhosis/therapy , Paracentesis , Adult , Aged , Atrial Natriuretic Factor/blood , Blood Component Removal , Female , Humans , Infusions, Intravenous , Liver Cirrhosis/blood , Male , Middle Aged , Prospective Studies , Recurrence , Renin/blood , Serum Albumin/administration & dosage
5.
Orv Hetil ; 138(49): 3121-4, 1997 Dec 07.
Article in Hungarian | MEDLINE | ID: mdl-9432656

ABSTRACT

A case of orthotopic liver transplantation (OLT) for secondary Neuroendocrine Tumor (NET), whose primary site was not detected at the time of surgery, is reported. The primary pancreatic lesion was found 20 months later in association with recurrence of neoplasm in the graft and with a paraneoplastic syndrome peculiar of glucagonoma. The patient started octreoide therapy with a decrease of the glucagone level but without reduction of the tumor size, nor disappearance of the clinical syndrome. A few months later the primary lesion was surgically removed, but her general condition deteriorated and the patient died waiting for liver retransplantation. A discussion about the management and the diagnostic tools for preoperative staging of these neoplasms and their ability to identify the primitive and secondary location of neuroendocrine tumors is presented.


Subject(s)
Liver Neoplasms/secondary , Liver Transplantation , Neuroendocrine Tumors/pathology , Pancreatic Neoplasms/pathology , Adult , Fatal Outcome , Female , Humans , Liver Neoplasms/surgery , Neuroendocrine Tumors/surgery , Pancreatectomy , Pancreatic Neoplasms/surgery
6.
Clin Transplant ; 10(4): 374-8, 1996 Aug.
Article in English | MEDLINE | ID: mdl-8884111

ABSTRACT

We report two cases of Kaposi's sarcoma in recipients of solid organ transplants, presenting (Case 1) 12 months after liver transplantation and (Case 2) 7 months after kidney transplantation. Both patients share the following features: natives from the Mediterranean area (Southern Italy), multiple immunosuppressive regimen, infection with hepatitis B and cytomegalovirus. During the 3 yr of follow-up after the diagnosis, their immunosuppressive regimen was reduced and they were treated with alpha interferon with remission of the clinical findings. The management of Kaposi's sarcoma in organ transplant recipients remains a controversial issue because of the risks of organ rejection associated with the reduction of immunosuppression and with the use of interferon.


Subject(s)
Interferon-alpha/therapeutic use , Kidney Transplantation , Liver Transplantation , Sarcoma, Kaposi/therapy , Skin Neoplasms/therapy , Adult , Cyclosporine/adverse effects , Cytomegalovirus Infections/complications , Hepatitis B/complications , Humans , Immunosuppressive Agents/adverse effects , Male , Postoperative Complications
7.
Dig Dis ; 14(3): 145-56, 1996.
Article in English | MEDLINE | ID: mdl-8861522

ABSTRACT

Ascites is a common complication of chronic liver disease. Treatment of the underlying liver disease with modalities such as abstinence from alcohol in Laennec's cirrhosis, phlebotomy in hemochromatosis, copper removal in Wilson's disease, and steroids in autoimmune liver disease, can improve survival in many patients. In addition, therapy of ascites alleviates the symptoms and improves the quality of life of the patients, and probably decreases the incidence of life-threatening conditions including spontaneous bacterial peritonitis and hepatorenal syndrome. The mean survival rate at 2 years is approximately 50%. Precipitating factors such as gastrointestinal bleeding, nonsteroidal anti-inflammatory drugs and infections, should be identified, since most of them can be corrected. Most cirrhotics with ascites can be managed with a 'step-by-step' approach, including dietary salt restrictions, aldosterone antagonists, and loop diuretics. When tense or refractory ascites is present, large-volume paracentesis is safe and effective. Peritoneovenous shunting (i.e. Denver, LeVeen) is less frequently used because of perioperative morbidity and mortality, and thrombotic complications with occlusion of the stent. Reinfusion of concentrated ascites is of potential benefit and has been used in Europe. Transjugular intrahepatic portosystemic shunt (TIPS) is an alternative procedure performed by interventional radiologists that allows decompression of portal hypertension. In many cases, ascites is improved after TIPS, but long-term randomized trials for tense or refractory ascites comparing TIPS with standard therapy are not conclusive. Liver transplantation is the ultimate step for the treatment of ascites, providing the cure for the underlying liver disease as well. Transplantation is indicated when quality of life of the patient is impaired due to recurrent episodes of ascites, or in the presence of spontaneous bacterial peritonitis and hepatorenal syndrome.


Subject(s)
Ascites/therapy , Ascites/etiology , Chronic Disease , Diuretics/therapeutic use , Humans , Liver Diseases/complications , Liver Diseases/surgery , Liver Transplantation , Paracentesis , Peritoneovenous Shunt , Portasystemic Shunt, Transjugular Intrahepatic
8.
Gastroenterology ; 109(1): 217-23, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7797019

ABSTRACT

BACKGROUND & AIMS: It has recently been described that kappa-opioid receptor agonists inhibit antidiuretic hormone secretion and promote water excretion in humans and experimental animals. The aim of this study was to evaluate the aquaretic efficacy of the kappa-opioid receptor agonist RU 51599 in conscious cirrhotic rats with ascites and water retention. METHODS: In protocol 1, arterial pressure, heart rate, and renal water metabolism were measured in basal conditions and then were measured for 120 minutes after the administration of Ringer's solution (n = 8; 0.4 mL) or RU 51599 (n = 7; 1 mg/kg). In protocol 2, plasma antidiuretic hormone concentration was measured (n = 6) before and 60 minutes after administration of RU 51599 (1 mg/kg). In protocol 3, the effect of RU 51599 (n = 9; 1 mg/kg) was compared with that of the V2-receptor antagonist SKF 100398 (n = 9; 30 micrograms/kg). RESULTS: RU 51599 administration induced a profound diuretic and aquaretic effect without altering arterial pressure and heart rate. In protocol 2, the kappa-opioid agonist reduced by about 50% plasma antidiuretic hormone levels (from 6.6 +/- 0.9 to 3.4 +/- 0.6 pg/mL; P < 0.05). Finally, the improvement in renal water metabolism induced by RU 51599 was similar to that produced by the V2-receptor antagonist. CONCLUSIONS: RU 51599 has a potent aquaretic effect in cirrhotic rats with water retention, suggesting that kappa-opioid receptor agonists may be useful for the treatment of water retention and dilutional hyponatremia in cirrhosis.


Subject(s)
Benzeneacetamides , Body Water/metabolism , Diuresis/drug effects , Liver Cirrhosis, Experimental/physiopathology , Pyrrolidines , Receptors, Opioid, kappa/agonists , Analysis of Variance , Animals , Arginine Vasopressin/analogs & derivatives , Arginine Vasopressin/pharmacology , Ascites , Blood Pressure/drug effects , Heart Rate/drug effects , Kidney/drug effects , Kidney/metabolism , Liver Cirrhosis, Experimental/metabolism , Male , Natriuresis/drug effects , Rats , Rats, Wistar , Receptors, Opioid, kappa/metabolism , Vasopressins/antagonists & inhibitors , Vasopressins/blood
9.
Transpl Int ; 8(1): 51-4, 1995.
Article in English | MEDLINE | ID: mdl-7888052

ABSTRACT

We measured the plasma levels of atrial natriuretic factor (ANF) during orthotopic liver transplantation (OLT) in eight adult patients with cirrhosis and ascites. The aim of this study was to determine whether significant differences in ANF concentration may be detected during the individual phases of OLT and to correlate these changes with hemodynamics. In each patient a hemodynamic assessment was achieved using a Swan-Ganz fiber optic catheter for continuous monitoring of cardiac output (CO), systemic vascular resistance index (SVRI), right filling pressure as assessed by central venous pressure (CVP), and left filling pressure by means of pulmonary arterial wedge pressure (PAWP). During reperfusion a clear-cut increase in ANF values was observed (P < 0.05). Concurrently, an increase in CVP (P < 0.05) and a decrease in SVRI were observed without any significant increase in diuresis. These data suggest that ANF might play a role in the development of the reperfusion syndrome.


Subject(s)
Atrial Natriuretic Factor/blood , Budd-Chiari Syndrome/blood , Liver Cirrhosis/blood , Liver Transplantation , Adult , Budd-Chiari Syndrome/surgery , Hemodynamics , Humans , Liver Circulation , Liver Cirrhosis/surgery , Reperfusion
10.
Dig Dis Sci ; 38(5): 903-8, 1993 May.
Article in English | MEDLINE | ID: mdl-8482189

ABSTRACT

A new method for concentrated ascitic fluid reinfusion using a double ultrafiltration device is reported as 22 procedures in 20 cirrhotic patients (6 females, 14 males; median age 55 years, range 33-69) with tense, refractory ascites. Eight of the 20 patients had elevated creatinine levels. The mean time for each procedure was 189 +/- 82 min, during which a mean of 7.7 liters (1.3-13.3) of ultrafiltered ascitic fluid was removed and 613 ml (140-1700) of concentrated ascitic fluid rich in albumin (mean: 60 g, range 14-175) was reinfused. The procedure resulted in a mean weight loss of 8.1 kg (2.2-14.0) and a mean increase of 163 ml in urine output (24 hr). A reduction in the serum creatinine level (P < 0.05) and an increase in the plasma atrial natriuretic factor level (P < 0.02) 24 hr after reinfusion, while no changes in serum albumin, plasma and urinary electrolytes, plasma renin activity, aldosterone, and antidiuretic hormone levels were noted. Although minor evidence for a disturbance in coagulation was observed, there were no episodes of clinical bleeding. Four patients (20%) had transient chills or fever. Based upon this experience, it can be concluded that reinfusion of cascade filtered and concentrated ascitic fluid is a rapid, safe, and effective treatment for patients with tense ascites; it appears to have less side effects than more traditional methods and importantly does not require administration of heterologous plasma derivatives.


Subject(s)
Ascites/therapy , Ascitic Fluid , Adult , Aged , Female , Hormones/blood , Humans , Male , Middle Aged , Serum Albumin/analysis , Ultrafiltration
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