ABSTRACT
UNLABELLED: This study evaluated the ability of young adults to respond to a simulated cardiac arrest using an automated external defibrillator (AED). METHOD: The study population was first-year medical students. None had received their mandatory training in emergency medicine. They role-played in pairs and entered a room in which a third person was lying on the floor and simulating unconsciousness and respiratory arrest. An AED and the corresponding poster-format instructions were clearly visible in the room, next to a telephone. The actions of pairs of responders were recorded. RESULTS: Interpretable results were obtained for 90 pairs of subjects. Most (96%) assessed vital signs and 20% performed this assessment correctly. Chest compressions were performed by 57%, 71% called emergency services, 4.5% removed the AED from the wall (but only one pair used it) and 8.9% did nothing. For 41% of the pairs, at least one member already had a cardiopulmonary resuscitation (CPR) certificate. The only statistically significant difference between students with and without a CPR certificate concerned use of the telephone to call emergency services. DISCUSSION: Despite the presence of an AED next to the telephone, the defibrillator was almost never used by the participants. Four out of ten pairs did not start chest compressions. The absence of any significant differences in performance between students with and without a CPR certificate casts doubt on the efficacy of the CPR training they had received. CONCLUSION: Results indicate the need for greater awareness of how to deal with cardiac arrest and the use of an AED when one is available.
Subject(s)
Defibrillators , Out-of-Hospital Cardiac Arrest/therapy , Patient Simulation , Students, Medical , Adolescent , Adult , Female , Humans , Male , Prospective Studies , Young AdultABSTRACT
BACKGROUND: The efficacy and safety of sublingual immunotherapy (SLIT) in patients with chronic rhinitis related to sensitization to house dust mites are still controversial. METHODS: After application of an anti-mite mattress cover, patients were only included in the study when the cumulative symptom score over a fortnight was greater than 70 out of a possible total of 168. Thirty-two of the 120 patients selected were randomized to receive SLIT for 2 years: 17 received placebo and 15 received the Dermatophagoides pteronyssinus and D. farinae 50/50 allergen extract. RESULTS: Significant between-group differences were observed after 1 year and persisted at the end of the second year for the rhinitis total score (P < 0.02), blocked nose score (P < 0.01) and nasal itching score (P < 0.01). Skin reactivity to house dust mites was significantly reduced in the group receiving house dust mite extract (P < 0.03). No statistical difference was observed between the two groups for medication scores, but a low medication consumption was observed in all patients. No serious and no systemic adverse reactions were reported. CONCLUSION: This study indicates the superiority of active treatment vs. placebo, evaluated on efficacy criteria (rhinitis score) or objective criteria (skin reactivity). The availability of a solid form (tablet) could represent a progress in terms of patient acceptability.
Subject(s)
Dust , Immunotherapy/methods , Mites/immunology , Rhinitis, Allergic, Perennial/immunology , Rhinitis, Allergic, Perennial/therapy , Administration, Sublingual , Adolescent , Adult , Animals , Antigens, Dermatophagoides/administration & dosage , Child , Dermatitis, Allergic Contact/immunology , Dermatitis, Allergic Contact/therapy , Dose-Response Relationship, Drug , Environmental Exposure , Female , Humans , Immunotherapy/adverse effects , Male , Nasal Provocation Tests , Rhinitis, Allergic, Perennial/diagnosis , Rhinitis, Allergic, Perennial/physiopathology , Skin Tests , Tablets , Treatment OutcomeABSTRACT
BACKGROUND: Optimal strategies to maintain short-term benefits of an initial rehabilitation program (RP) are not known. To assess the long-term effects of exercise maintenance (EM) after an initial outpatient RP, the authors conducted a prospective study. PATIENTS AND METHODS: Fifty-eight patients with moderate to moderately severe chronic obstructive pulmonary disease who completed an initial 7-week outpatient RP were included. They were allocated into four groups according to the conditions of EM they self-selected: 15 patients received a structured EM session supervised by a physiotherapist twice a week (group A); 14 patients received a structured EM session supervised by a physiotherapist once a week (group B); 15 patients continued self EM daily at home (group C); and 14 patients did not continue EM (group D). Patients were evaluated before, immediately after, and 18 months after the initial outpatient RP. Measurements included exercise testing on a cycle ergometer and a visual analog scale to evaluate chronic dyspnea. RESULTS: After RP, all patients exhibited improvements in maximal workload (P < 0.05) and in dyspnea (P < 0.05). Improvements in maximal workload were maintained at 18 months in patients in groups A, B, and C but these only reached significance in groups B and C (P < 0.05). On the other hand, maximal workload returned to baseline values in group D (P = 0.01) at 18 months. CONCLUSION: Our results indicate definite benefits of EM after an initial outpatient RP compared with no EM. Daily EM at home appears to be as efficient as structured EM sessions supervised by a physiotherapist, once or twice a week, in moderate to moderately severe chronic obstructive pulmonary disease.
Subject(s)
Exercise Therapy/methods , Lung Diseases, Obstructive/rehabilitation , Outpatients , Aged , Exercise Test , Female , Follow-Up Studies , Humans , Lung Diseases, Obstructive/diagnosis , Lung Diseases, Obstructive/physiopathology , Male , Middle Aged , Prospective Studies , Respiratory Function Tests , Severity of Illness Index , Treatment OutcomeABSTRACT
Respiratory rehabilitation is a multidisciplinary medical approach which allows a total care of patients suffering from COPD. Optimisation of bronchodilator treatment, health education, cessation of smoking, dietetic, relaxation and re-entrainment to effort. We report out experience concerning 88 BPCO (mean age 62.1, FEV1 of 1.4 litres; or 48% of predicted normal); these 88 patients were cared for on an ambulatory basis at our centre for two hours per session, three times per week for seven weeks. The objective results were analysed on exercise tests before and after treatment. For ventilation, there was a significant improvement in the power developed (from 45.5+/-17.1 to 53.4+/-23 watts; p<0.001) without any change in the oxygen consumption (VO2), ventilation (VE) or heart rate (FC) and of oxygen pulse (VO2/FC). For the same level of power (80% of maximum power for the initial exercise test) there was a significant lowering of ventilation (V=33.5+/-9.4 to 30.7+/-7.4 litres per minute, p<0.001), cardiac frequency (FC: from 116.9+/-16 to 111.1+/-13.1 beats per minute, p<0.001) as well as the oxygen pulse (VO2/FC: from 7.9+/-2.7 to 8.3+/-3.7). At the maximum on the exercise test all the parameters studied were significantly better: watts, VO2, VE, cardiac frequency and VO2/FC. A study of the visual analogue scale (EVA), analysing sleep, anxiety, dyspnoea and the physical aspects showed a significant improvement in the four subjective parameters. Respiratory rehabilitation of BPCO practiced as an out patient has shown an improvement in exercise tolerance in every day activities and improvement in dyspnoea and in the quality of life.
Subject(s)
Ambulatory Care , Exercise Tolerance , Lung Diseases, Obstructive/rehabilitation , Quality of Life , Aged , Exercise Test , Female , Forced Expiratory Volume , Humans , Lung Diseases, Obstructive/physiopathology , Lung Diseases, Obstructive/psychology , Male , Middle Aged , Oxygen Consumption , Patient Care Team , Patient Education as Topic , Program EvaluationABSTRACT
The aim of this prospective study was to analyse the contribution of the measurement of alveolar arterial gradients of CO2 during forced expiration in the diagnosis of pulmonary emboli occurring in chronic airflow obstruction (COPD) as a result of smoking. The study was carried out on 178 patients: Group 1: 54 subjects without emboli (14 controls, 33 COPD and 7 patients with chest pain); Group 2: 72 patients with proved emboli (49 non COPD, 23 COPD); Group 3: 52 patients COPD presenting with varied non-embolic broncho-pulmonary pathology (pneumonia, bronchospasm, pulmonary oedema, bronchial neoplasm). The diagnosis of pulmonary emboli was confirmed by scintigraphy in patients with non COPD or angiography (in patients with COPD). The maximal fraction of CO2 was measured using a capnologue during a forced expiration which was long and prolonged until residual volume was achieved. The PaCO2 was measured simultaneously by an analysis of arterial blood gases. The D index was calculated according to the formula [(PaCO2-PEM CO2)/PaCO2] x 100. The D index was significantly lower in Group 1 (3.42 +/- 3.8% p < 0.0001) than in Group 2 (20.8 +/- 10%) and Group 3 (17.6 +/- 11.7%) (not significant between Groups 2 and 3). In patients with COPD the specificity and sensitivity and the predicted positive and negative value were 100% for a D limit of 7%. In COPD patients these values were respectively 82, 95, 75 and 96% for a D limit of 7%; on the other hand for a D below 5% the values were 60, 100, 64 and 100% respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
Subject(s)
Carbon Dioxide/metabolism , Lung Diseases, Obstructive/metabolism , Pulmonary Embolism/diagnosis , Adult , Aged , Bronchial Neoplasms/metabolism , Bronchial Spasm/metabolism , Carbon Dioxide/blood , Chest Pain/metabolism , Female , Forced Expiratory Flow Rates , Humans , Lung Diseases, Obstructive/complications , Male , Maximal Expiratory Flow Rate , Middle Aged , Monitoring, Physiologic/instrumentation , Pneumonia/metabolism , Prospective Studies , Pulmonary Edema/metabolism , Pulmonary Embolism/etiology , Residual Volume , Sensitivity and Specificity , Smoking/adverse effectsSubject(s)
Asthma/drug therapy , Beclomethasone/therapeutic use , Bronchitis/drug therapy , Adult , Aerosols , Beclomethasone/administration & dosage , Female , Humans , Male , Middle AgedSubject(s)
Bronchial Neoplasms/surgery , Lipoma/surgery , Adult , Aged , Bronchial Neoplasms/diagnosis , Bronchial Neoplasms/pathology , Humans , Lipoma/diagnosis , Lipoma/pathology , Male , Middle AgedSubject(s)
Asthma/drug therapy , Beclomethasone/therapeutic use , Bronchitis/drug therapy , Adult , Chronic Disease , Clinical Trials as Topic , Female , Humans , Male , Middle AgedSubject(s)
Bronchial Neoplasms/diagnosis , Bronchoscopy/methods , Lung Neoplasms/diagnosis , Adult , Aged , Evaluation Studies as Topic , Female , Fiber Optic Technology , Humans , Male , Middle AgedABSTRACT
Acids mucins were isolated from a mixture of bronchial washings carried out on 5 subjects, in macroscopically healthy areas of the bronchial tree. Neutral mucins were absent.