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1.
J Hosp Infect ; 41(1): 11-8, 1999 Jan.
Article in English | MEDLINE | ID: mdl-9949959

ABSTRACT

Three prevalence studies for the estimation of hospital-acquired infections (HAIs) were carried out in eight Greek hospitals on an annual basis during the years 1994-1996. The overall prevalence of HAI was 6.8, 5.5 and 5.9% for the three years, respectively. Among these, urinary tract infections ranged from 22.4 to 38.2%, lower respiratory tract infections ranged from 21.1 to 32.6%, surgical site infections ranged from 14.6 to 22.7% and bloodstream infections ranged from 9.0 to 13.2%. The prevalence of antibiotic usage among the hospitalized patients was found to be 49.3% in 1994, 47.3% in 1995 and 52.7% in 1996. Unjustified prescription of prophylactic usage was found to be the major component of these high percentages. Appropriate use of antibiotics for prophylaxis is one of the priorities of the current infection control programmes. The development of a nationwide network for the surveillance of HAIs in Greece is planned using the experience gained.


Subject(s)
Cross Infection/epidemiology , Adolescent , Adult , Age Distribution , Aged , Anti-Bacterial Agents/therapeutic use , Child , Child, Preschool , Cross Infection/drug therapy , Data Collection , Drug Utilization/statistics & numerical data , Greece/epidemiology , Humans , Infant , Middle Aged , Morbidity/trends , Pilot Projects , Prevalence
2.
Vet Hum Toxicol ; 39(3): 155-7, 1997 Jun.
Article in English | MEDLINE | ID: mdl-9167245

ABSTRACT

Reports of acute turpentine intoxication, particularly containing toxicological data, are poorly verified in the literature. This report regards the intentional massive ingestion of turpentine solution in an elderly woman who developed mainly central nervous system manifestations, then had an impressive and quick total recovery although the initial prognosis was very bad. Blood and urine levels of turpentine were monitored using gas chromatography and at the early toxicogenic stage were 28 micrograms/mL and 15 micrograms/mL respectively. Gastric fluid analysis on admission to the hospital revealed the presence of approximately 200 mL turpentine in the intestine. A review of earlier reports is given.


Subject(s)
Solvents/poisoning , Turpentine/poisoning , Administration, Oral , Aged , Aged, 80 and over , Female , Gastric Lavage , Humans , Respiration, Artificial , Solvents/administration & dosage , Solvents/metabolism , Turpentine/administration & dosage , Turpentine/metabolism
3.
J Clin Forensic Med ; 4(3): 133-7, 1997 Sep.
Article in English | MEDLINE | ID: mdl-15335573

ABSTRACT

Although poisonings (fatal and non-fatal) due to intentional or accidental acute exposure to toluene or toluene mixture fumes have been previously reported in the literature, several issues concerning lethal doses or lasting post-exposure neuropathological impairments still remain unclear. Two male painters (18 and 30 years old) were accidentally exposed to toxic concentrations of paint diluent fumes containing toluene (TL), acetone (ACT) and methyl ethyl ketone (MEK) (60:15:15 w/w/w respectively) during their work in an underground reservoir. Both workers were found unresponsive by colleagues and were immediately transferred to the regional hospital. On admission, the younger man was pronounced dead, while the other remained in the intensive care unit for 3 days and then 4 days in the internal medicine ward. TL, ACT and MEK concentrations in blood samples taken from the survivor on admission were 6.3, 30.6 and 40.5 microg/mL. Postmortem toxicology of the dead worker revealed TL, ACT and MEK blood levels of 12.4, 90.8 and 80.4 microg/mL respectively. The solvent levels in the liver, kidney, lung, brain, testis and gland were also quantified and showed a somewhat similar distribution of the chemicals among these tissues with the highest levels found in the brain and the liver. The fatal and the non-fatal outcome that resulted despite similar intoxication conditions, most probably demonstrates the interindividual tolerance among the painters who also had similar body weights. The surviving painter did not develop any neuropsychological impairment in post-exposure time. The reported case strongly emphasizes the necessity to take precautions when using paint diluents in enclosed spaces.

4.
Vet Hum Toxicol ; 38(2): 101-7, 1996 Apr.
Article in English | MEDLINE | ID: mdl-8693683

ABSTRACT

Nine human acute poisonings due to intentional ingestion of organophosphorous pesticides are presented. Six of the victims died. Six patients were treated in the Intensive Care Unit (ICU) from 34 h to 45 d, while 3 were found dead by relatives. Two of the patients treated in the ICU fully recovered after 15 and 24 d while the third survivor developed delayed neuropathy. Organophosphate blood levels were determined on admission and during therapy, and in 1 case atropine and pralidoxime levels were also detected. Significant fluctuations of the plasma cholinesterase activity were observed during therapy. Postmortem analysis revealed higher levels of pesticides in organs (eg 23.1 micrograms fenthion/g kidney) and in fat (135.2 micrograms fenthion/g) than in blood (eg 4.8 micrograms fenthion/ml) and vitreous humor. Considerable pesticide was measured in testis (eg 5.8 micrograms fenthion/g, 0.8 micrograms methidathion/g) and uterus (170.5 micrograms malathion/g). Extracorporeal decontamination to enhance pesticide elimination is a therapeutic challenge.


Subject(s)
Insecticides/poisoning , Suicide, Attempted/statistics & numerical data , Suicide/statistics & numerical data , Adult , Aged , Cholinesterase Inhibitors/blood , Cholinesterase Inhibitors/pharmacokinetics , Cholinesterase Inhibitors/poisoning , Dimethoate/blood , Dimethoate/pharmacokinetics , Dimethoate/poisoning , Female , Fenthion/blood , Fenthion/pharmacokinetics , Fenthion/poisoning , Greece/epidemiology , Humans , Insecticides/blood , Insecticides/pharmacokinetics , Intensive Care Units , Kidney/drug effects , Kidney/metabolism , Malathion/blood , Malathion/pharmacokinetics , Malathion/poisoning , Male , Middle Aged , Organophosphate Poisoning , Organothiophosphates/blood , Organothiophosphates/pharmacokinetics , Organothiophosphorus Compounds/blood , Organothiophosphorus Compounds/pharmacokinetics , Organothiophosphorus Compounds/poisoning , Phosphamidon/blood , Phosphamidon/pharmacokinetics , Phosphamidon/poisoning , Poisoning/mortality , Testis/drug effects , Testis/metabolism , Tissue Distribution , Uterus/drug effects , Uterus/metabolism
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