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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical & experimental allergy 18 (1988), S. 0 
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Allergy 45 (1990), S. 0 
    ISSN: 1398-9995
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: To elucidate whether systemic reactions (SR) to drugs should be included in the atopic status in epidemiological studies, we compared the distribution of atopy in subjects with or without a history of SR to drugs. The studied population comprised 2067 adults, 20 to 60 years old, visiting a health care center for a check-up examination. The protocol included a questionnaire related to history of SR to drugs and a Phadiatop® test which evaluates on a blood sample the presence of specific IgE against common aeroallergens. Overall, 14.7% of the study group, including 66% women, reported reliable histories of SR to drugs. The cumulative prevalence of asthma, hay fever and childhood dermatitis was higher in the SR group. By contrast, the percentage of positive Phadiatop tests was similar in subjects with or without a history of SR. Thus atopy, defined by an objective criterion, i.e. the presence of specific IgE against common aero-allergens, is not associated with the occurrence of SR to drugs. Such a history should not be included as part of the atopic status.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1254
    Keywords: Air pollution ; Pulmonary function ; Epidemiology ; Children
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geography , Physics
    Notes: Abstract In the literature, studies devoted to shortterm effects of air pollution episodes in children have provided controversial results. To evaluate if acute air pollution changes in the Gardanne coal basin (France) could have deleterious effects on children's pulmonary function, we studied 160 children on two different days. Each in-school examination consisted of a short questionnaire and a spirometric assessment. The area included districts of high and low pollution levels. In the former, the two examinations took place at different air pollution levels whereas, in the latter, the air pollution levels were comparable. We obtained higher spirometric values during the second examination, regardless of air pollution changes and suggesting a learning effect, which vanished when we used FEV1/FVC ratio. The difference in FEV1/FVC between days of low and high pollution was significant but merely equal to 2%. There was no change of clinical symptom score.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1569-8041
    Keywords: long-term survival ; prognostic factors ; small-cell lung cancer ; treatment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background: The aim of this study was to analyze SCLC patients beyond 30 months, particularly their outcome, their way of life, and factors which could influence relapses, second-primary cancers and death. Patients and methods: Between January 1986 and May 1995, 263 SCLC patients who survived longer than 30 months were included from 52 French institutions. The analysis was performed on the 155 cases confirmed by a pathologic review. Results: Physical, mental and psychological states were considered as normal at 30 months in respectively 70.3%, 87.7% and 67.7% of patients, not influenced by prophylactic cranial irradiation, number of chemotherapy cycles, CCNU or cisplatin. Therapeutic sequelae were neurological impairment (13%), pulmonary fibrosis (18%) and cardiac disorders (11%) at 30 months. Return to work was possible for 40% of patients in the first two years following diagnosis. Among 43 relapsing patients, 33 benefited from a second-line treatment. Their median survival was 12 months since retreatment, and seven patients have survived again longer than 30 months. Age 〉60 at the time of diagnosis was found as an independent factor increasing the risk of relapse beyond 30 months (OR = 2.46, IC 95% (1.16–5.26), P = 0.01). The risk of relapse became less than 10% beyond five years. Twenty patients (13%) developed a second primary cancer in a mean time of 58.6 months. The risk of second primary cancer was increased by a number of chemotherapy cycles 〉6 (OR = 3.25, IC 95% [1.08-9.8] P = 0.02) and by an age 〉60 (OR = 2.92, IC 95% (1.07–7.97), P = 0.03). Five- and 10-year survival rates were respectively 68% and 44%. In these patients having reached a 30-month survival, three independent factors were predictive of a survival longer than five years: age ≤60 at the time of diagnosis (OR = 2.85, IC 95% (1.23–6.6), P = 0.01), chest radiotherapy (OR = 3.1, IC 95% (1.28–7.69), P = 0.006) and absence of relapse (OR = 4.5, IC 95% (1.75–12.5), P = 0.002). This study suggests that: 1) therapeutic sequelae are rather mild, allowing return to work in 40% of patients; 2) relapsing 30-month survivors can benefit from second-line treatment; 3) SCLC cure can be achieved with a 10-year follow-up.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1569-8041
    Keywords: cisplatin ; delayed emesis ; dexamethasone ; granisetron ; 5-HT3-receptor antagonist ; oral antiemetic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background: The efficacies of granisetron plus dexamethasone anddexamethasone alone in controlling delayed nausea and vomiting aftercisplatin chemotherapy (≥69 mg/m2) were compared in amulticentre, double-blind, placebo-controlled comparative study. Patients and methods: In all, 654 patients (of whom 619 were evaluable)received prophylactic granisetron plus dexamethasone before chemotherapy onday 0; on day 1 complete responders and non-responders were randomizedseparately to receive dexamethasone, 8 mg b.d. p.o., with eithergranisetron, 1 mg b.d. p.o., or matching placebo for six days. Results: Over days 1–6 the complete response rates were54.5% (dexamethasone group) and 52.1% (dexamethasone plusgranisetron group). Response rates were higher over days 4–6(71.8% and 70.7%, respectively) than over days 1–3(60.4% and 57.9%, respectively). Significantly more patientswho responded to antiemetic treatment during day 0 were responders over days1–6 (63% vs. 17%; P 〈 0.001). No othertreatment-related differences were found. Adverse events tended to be minor,with constipation and headache the most common. Overall, there were nosignificant differences in the safety profiles of the two regimens, butconstipation and abdominal pain were significantly more common in thedexamethasone plus granisetron group. Conclusions: Granisetron plus dexamethasone did not appear to conferadditional benefit over use of dexamethasone alone in controlling delayednausea and vomiting following cisplatin chemotherapy. Control of acute nauseaand vomiting, however, appeared to be an important factor influencing delayednausea and vomiting.
    Type of Medium: Electronic Resource
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