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1.
Eur J Anaesthesiol ; 24(11): 942-50, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17681089

ABSTRACT

BACKGROUND AND OBJECTIVE: Epidural and intravenous analgesia are widely used for postoperative pain management. Efficacy and safety is enhanced with the establishment of acute pain services. We studied the terms of application of these techniques in Greek hospitals and compared practices between anaesthetic departments with or without acute pain services. METHODS: We performed a postal survey regarding departmental policy on the application of epidural and intravenous analgesia, patient monitoring, audit and educational activities, acute pain service teams and proposals for improvement. Pain services were classified according to predetermined quality criteria. Hospitals with or without acute pain services were compared. RESULTS: Response rate was 46.3% (51 of 110 departments). Epidural analgesia was used in 49 departments, equally applied as intermittent boluses or continuous infusion. Twenty-two of the 39 departments that were using continuous infusion, used exclusively a lumbar approach. Intravenous analgesia was used by 42 (82%) departments; 13 used exclusively continuous infusion. All eight departments that had an established acute pain service fulfilled the predefined quality criteria compared with only ten of the remaining 43 (P < 0.001). CONCLUSION: Our study discloses important issues regarding the use of intravenous and epidural analgesia and postoperative patient monitoring in Greek hospitals. Implementation of acute pain services that are satisfying the quality criteria may help to improve patient care.


Subject(s)
Analgesia, Epidural/statistics & numerical data , Analgesics/administration & dosage , Pain, Postoperative/drug therapy , Analgesia, Patient-Controlled , Analgesics, Opioid/therapeutic use , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Antiemetics/therapeutic use , Drug Utilization , Greece , Health Care Surveys , Health Facility Size , Humans , Injections, Intravenous , Pain Clinics , Pain, Postoperative/classification , Surveys and Questionnaires
2.
Nephron Exp Nephrol ; 96(1): e14-22, 2004.
Article in English | MEDLINE | ID: mdl-14752244

ABSTRACT

BACKGROUND: Complement deficiency predisposes to autoimmune renal disease. Since complement deficient mice are increasingly used to study the immunopathogenesis of renal disease we have determined whether mice deficient in C3 or C4 are susceptible to spontaneous immune-mediated renal injury. METHODS: C3-deficient, C4-deficient and complement-sufficient, wild-type mice were maintained in standard conditions for 1 year at which stage renal function, renal histology, circulating antibody and autoantibody levels were assessed. RESULTS: No significant decline in renal function was demonstrated in the complement-deficient mice. However, there was histological evidence of glomerular injury in both the C3- and C4-deficient mice, but of insufficient severity to alter function. Serum IgG2a concentration was significantly lower in C3- and C4-deficient mice. In contrast C3-deficient mice had higher concentrations of serum IgG2b. There was a tendency for mice from all groups, including the complement-sufficient mice, to develop autoantibodies. C4-deficient mice had higher titres of anti-dsDNA IgG but otherwise deficient mice had similar autoantibody titres to controls. CONCLUSION: We conclude that C4-deficient mice demonstrate a small increase in autoantibody production at 1 year of age compared to C3-deficient and wild-type mice. Furthermore, although complement-deficient mice exhibit glomerular changes, they are of minor functional significance, and are unlikely to affect the study of experimentally induced renal disease in these mice.


Subject(s)
Autoimmune Diseases/physiopathology , Complement C3/deficiency , Complement C4/deficiency , Kidney Glomerulus/pathology , Kidney Glomerulus/physiopathology , Animals , Autoantibodies/biosynthesis , Autoantibodies/blood , Autoimmune Diseases/blood , Autoimmune Diseases/pathology , Female , Frozen Sections/methods , Glomerulonephritis/blood , Glomerulonephritis/pathology , Glomerulonephritis/physiopathology , Immunoglobulin G/biosynthesis , Immunoglobulin G/blood , Immunoglobulin M/biosynthesis , Immunoglobulin M/blood , Immunohistochemistry/methods , Kidney Glomerulus/immunology , Mice , Mice, Inbred C57BL , Mice, Inbred Strains , Mice, Mutant Strains
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