Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
1.
Article in English | IMSEAR | ID: sea-46934

ABSTRACT

The present study compared the efficacy of preloading with colloid "Haemaccel" with vasoconstrictor (intravenous ephedrine sulphate) in preventing hypotension during propofol induction. This prospective, randomized study included 120 patients of Amercan Society of Anaesthesiologists (ASA) physical status I and II ageing 21 to 50 years of both gender coming for routine surgery. Patients were randomly allocated into three groups with 40 patients in each. Group A (control) did not receive any study medication, group B received Haemaccel (10 ml/kg intravenously over 10-15 minutes) and group C received injection ephedrine (0.2 mg/kg iv) prior to induction of anaesthesia. Propofol (2.5 mg/kg iv) was used for induction of anaesthesia. Heart rate and blood pressure were recorded before induction (baseline) and then every minute for 5 minutes after administering propofol. Anaesthesia was continued with standard technique thereafter. Hypotension was defined as fall in systolic blood pressure more than 20% from the basal value. The incidence of hypotension in Haemaccel (23.1%) or ephedrine group (22.5%) was significantly less than the control group (67.5%, P<0.01). We conclude that though preloading with colloid (Haemaccel) or prior injection of sympathomimetic (ephedrine) are not fully efficacious in preventing hypotension caused by propofol induction, both decrease the incidence in significant number of patients with heart rate less than baseline value in the colloid group.


Subject(s)
Adult , Anesthesia , Anesthetics, Intravenous/adverse effects , Ephedrine/administration & dosage , Female , Humans , Hypotension/chemically induced , Infusions, Intravenous , Injections, Intravenous , Male , Middle Aged , Plasma Substitutes/administration & dosage , Polygeline/administration & dosage , Propofol/adverse effects , Vasoconstrictor Agents/administration & dosage
2.
Article in English | IMSEAR | ID: sea-41905

ABSTRACT

OBJECTIVE: This prospective, randomized, double-blind study was designed to determine and compare the usefulness of preloading colloids (Haemaccel) 10 ml/Kg before positioning whether it can prevent hemodynamic changes during seated positioning or not. MATERIAL AND METHOD: The authors studied 20 patients by randomly dividing them into 2 groups. The control group was given crystalloid as maintenance and deposit replacement but the study group was given extra colloids 10 ml/Kg 30 minutes before starting general anesthesia. Both groups were monitored and given anesthesia, balanced technique. Systolic and diastolic blood pressures, heart rate, central venous pressure (CVP) at different time intervals in the sitting position for 30 minutes were recorded. Statistical analysis was done by Student t-test, Chi-square test and ANOVA (p-value < 0. 05 considered significant). RESULTS: The results showed that systolic blood pressure at 15, 20, 30 minutes and CVP at 15, 25, 30 minutes after positioning in the study group was maintained significantly compared to the control group and there were no significant changes in diastolic blood pressure and heart rate. There were no other complications during the sitting period. CONCLUSION: It is concluded that preloading colloid fluid prior to repositioning could prevent the decrease of systolic blood pressure and central venous pressure during sitting positioning without other complications.


Subject(s)
Adult , Blood Pressure/drug effects , Double-Blind Method , Female , Fluid Therapy/methods , Hemodynamics/drug effects , Humans , Male , Middle Aged , Neurosurgical Procedures , Plasma Substitutes/administration & dosage , Polygeline/administration & dosage , Posture/physiology , Preoperative Care , Prospective Studies
3.
Annals Abbassi Shaheed Hospital and Karachi Medical and Dental College. 2002; 7 (2): 396-398
in English | IMEMR | ID: emr-58920

ABSTRACT

Ascites is a frequently encountered problem in Cirrhotics and Total Abdominal Paracentesis is an easy and quick way of relieving these patients. To observe the Total Abdominal Paracentesis with IV Albumin or Hemaccel and observe systemic hemodynamics, electrolytes and renal function. Material and 30 patients who were admitted in A.S.H. were included in study. Patients with hepatocellular carcinoma, child Grade, increased Prothrombin time etc. were excluded. Out of 30 patients enrolled, one expired as he was erroneously included in study. In rest of patients all were hemodynamically stable after one day. Total Abdominal Paracentesis is a safe procedure and can be used to relieve patients with tenso ascites in fast and safe way


Subject(s)
Humans , Male , Female , Paracentesis , Liver Cirrhosis/complications , Albumins/administration & dosage , Albumins , Polygeline , Polygeline/administration & dosage
4.
Article in English | IMSEAR | ID: sea-65266

ABSTRACT

BACKGROUND: Patients with cirrhotic ascites have low serum albumin levels, and paracentesis of ascitic fluid could compromise them further. AIM: We compared the therapeutic efficacy of ascitic fluid filtration and concentrate infusion (AFI) versus total-volume paracentesis (TVP) with colloid infusion in control of tense or intractable cirrhotic ascites. METHODS: Ten patients underwent AFI; their ascitic fluid was filtered repeatedly through hollow-fiber hemodialyzer, and the concentrate reinfused intravenously. In ten patients TVP was done with simultaneous intravenous colloid infusion. Follow-up was done weekly and the study terminated if the patient needed diuretics or developed complications. RESULTS: Pre-study parameters were similar in the two groups. In the AFI and TVP groups, the duration of procedure was median 12 hours and 5.5 hours; fluid removed by paracentesis was 10.2 L and 8.0 L, respectively; and fluid infused intravenously was 0.5 L [with mean (SD) protein content 5.7 (1.3) g/dl] and 1.1 L, respectively. Glomerular filtration rates were lower than normal in the two groups but did not change significantly with the procedure; body weight remained significantly lower up to week 3 and week 2, respectively. The study was terminated at median week 3 (range 1-8) and week 2 (1-4), respectively. Fever was an accompaniment of AFI and one patient developed peritonitis. CONCLUSION: Patients undergoing AFI remained diuretic-free longer; the procedure is cost-effective but needs to be further evaluated to minimize the side-effects.


Subject(s)
Ascites/etiology , Body Weight , Cost-Benefit Analysis , Female , Humans , Infusions, Intravenous , Liver Cirrhosis/complications , Male , Middle Aged , Paracentesis , Plasma Substitutes/administration & dosage , Polygeline/administration & dosage , Random Allocation , Statistics, Nonparametric , Ultrafiltration/methods
SELECTION OF CITATIONS
SEARCH DETAIL