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1.
JAMA ; 274(15): 1221-5, 1995 Oct 18.
Article in English | MEDLINE | ID: mdl-7563512

ABSTRACT

OBJECTIVE: To test the hypothesis that prolonged motor recovery after long-term ventilation may be due to polyneuropathy and can be foreseen at an early stage by electromyography (EMG). DESIGN: Cohort study with an entry period of 18 months. Polyneuropathy was identified by EMG studies in the intensive care unit (ICU). During a 1-year follow-up, amount of time was recorded to reach a rehabilitation end point. SETTING: The general ICU of a community hospital. PATIENTS: Fifty patients younger than 75 years who were receiving mechanical ventilation for more than 7 days. MAIN OUTCOME MEASURES: A rehabilitation end point was defined as return of normal muscle strength and ability to walk 50 m independently. RESULTS: In 29 of 50 patients, an EMG diagnosis of polyneuropathy was made in the ICU. Patients with polyneuropathy had a higher mortality in the ICU (14 vs 4; P = .03), probably related to multiple organ failure (22 vs 11; P = .08) or aminoglycoside treatment of suspected gram-negative sepsis (17 vs 4; P = .05). Rehabilitation was more prolonged in 12 patients with polyneuropathy than in 12 without polyneuropathy (P = .001). Of nine patients with delays beyond 4 weeks, eight had polyneuropathy, five of whom had persistent motor handicap after 1 year. In particular, axonal polyneuropathy with conduction slowing on EMG indicated a poor prognosis. CONCLUSIONS: Polyneuropathy in the critically ill is related to multiple organ failure and gram-negative sepsis, is associated with higher mortality, and causes important rehabilitation problems. EMG recordings in the ICU can identify patients at risk.


Subject(s)
Convalescence , Nervous System Diseases , Respiration, Artificial , APACHE , Adult , Aged , Cohort Studies , Critical Illness/rehabilitation , Electromyography , Female , Humans , Male , Middle Aged , Multiple Organ Failure/complications , Nervous System Diseases/complications , Nervous System Diseases/epidemiology , Nervous System Diseases/physiopathology , Prognosis , Prospective Studies , Risk Factors , Sepsis/complications , Time Factors , Ventilator Weaning , Walking
2.
Intensive Care Med ; 15(7): 424-31, 1989.
Article in English | MEDLINE | ID: mdl-2689493

ABSTRACT

The efficacy of a relatively cheap regimen of selective decontamination (SDD) was evaluated in a diverse population of ICU patients. Patients requiring prolonged ICU stay (greater than 5 days) were randomly allocated to a treatment group or control group. Control patients (n = 52) received perioperative antimicrobial prophylaxis and antibiotic treatment was instituted only on sound clinical and bacteriological criteria. Treated patients (n = 48) received gastro-intestinal and oro-pharyngeal decontamination with polymyxin E, norfloxacin, amphotericin B and systemic antibiotic prophylaxis with trimethoprim until decontamination was achieved. The rate of gram-positive infections was not altered by SDD. The incidence of gram-negative respiratory tract, urinary tract and line infections was significantly reduced from 44%, 27% and 15% respectively in the control group to 6%, 4% and 0% in the treatment group. Mortality from nosocomial sepsis and overall mortality were also significantly reduced from 15% and 54% to 0% and 31% respectively. The ICU stay was not reduced by SDD, nor was time on the ventilator or use of therapeutic antibiotics. The reduction in morbidity and mortality was achieved at a relatively low cost.


Subject(s)
Bacterial Infections/prevention & control , Cross Infection/prevention & control , Digestive System , Intensive Care Units , Norfloxacin/therapeutic use , Respiratory System , Bacterial Infections/drug therapy , Bacterial Infections/epidemiology , Cross Infection/drug therapy , Cross Infection/epidemiology , Female , Gram-Negative Bacteria , Humans , Incidence , Male , Middle Aged , Norfloxacin/standards , Premedication , Prospective Studies , Randomized Controlled Trials as Topic
3.
Ann Thorac Surg ; 45(1): 24-7, 1988 Jan.
Article in English | MEDLINE | ID: mdl-3257375

ABSTRACT

In two groups of patients undergoing coronary artery bypass grafting (CABG), two different regimens of antibiotic prophylaxis with cefamandole nafate were compared. In Group 1, 30 mg per kilogram of body weight was administered intravenously during induction of anesthesia. In Group 2, a second dose of 15 mg/kg was administered intravenously shortly before cannulation. Serum and tissue levels in the right atrium, the pericardium, and the sternum were determined using high-pressure liquid chromatography. The results showed that in Group 2 the serum levels were significantly higher from 48 minutes onward after induction and remained at an acceptable level during CABG. The tissue levels in the sternum and pericardium were also significantly higher in Group 2 compared with Group 1. It is concluded that a second dose of cefamandole (15 mg/kg) shortly before the beginning of cardiopulmonary bypass is recommended, particularly for high-risk patients.


Subject(s)
Cefamandole/administration & dosage , Coronary Artery Bypass , Premedication , Cefamandole/blood , Cefamandole/pharmacokinetics , Drug Administration Schedule , Half-Life , Humans , Infusions, Intravenous , Prospective Studies , Random Allocation , Tissue Distribution
4.
Crit Care Med ; 14(9): 812-4, 1986 Sep.
Article in English | MEDLINE | ID: mdl-3488873

ABSTRACT

An arterial pH catheter was inserted into a femoral artery of 15 patients immediately after coronary artery bypass grafting. Catheter pH measurements correlated well with conventional blood gas measurements during the first 12 h postsurgery, and revealed rapid pH changes during weaning and bronchial suctioning. This device is a promising step in the development of a complete on-line blood gas analyzer.


Subject(s)
Acid-Base Equilibrium , Coronary Artery Bypass , Monitoring, Physiologic/instrumentation , Aged , Blood Gas Analysis/instrumentation , Catheters, Indwelling , Female , Femoral Artery , Humans , Male , Middle Aged , Postoperative Care/instrumentation
5.
J Hypertens Suppl ; 4(1): S107-10, 1986 Apr.
Article in English | MEDLINE | ID: mdl-2939209

ABSTRACT

Postoperative hypertension following coronary artery bypass grafting is usually treated with vasodilating agents like nitroprusside. In recent studies ketanserin, a 5-hydroxytryptamine type 2 antagonist, appeared to be effective in the treatment of this clinical syndrome. In 20 patients, divided into two comparable groups, nitroprusside and ketanserin were compared with respect to their haemodynamic and ventilatory profiles. The study showed that both agents were equally effective in decreasing the raised systolic blood pressure, but that ketanserin was more advantageous with respect to the absence of reflex tachycardia and the unchanged shunt fraction.


Subject(s)
Ferricyanides/therapeutic use , Hypertension/drug therapy , Nitroprusside/therapeutic use , Piperidines/therapeutic use , Blood Pressure , Coronary Artery Bypass , Female , Heart Rate , Humans , Hypertension/etiology , Ketanserin , Male , Middle Aged , Postoperative Complications/drug therapy , Pulmonary Artery , Vascular Resistance
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