scholarly journals Proceedings of a Workshop on Near Fatal Asthma

1995 ◽  
Vol 2 (2) ◽  
pp. 113-126 ◽  
Author(s):  
J Mark FitzGerald ◽  
Peter T Macklem

Concern has been expressed about rising asthma morbidity and mortality, although the latter appears to have declined recently. A reasonable surrogate for fatal asthma is an episode of near fatal asthma (NFA). The etiology of episodes of NFA appears to be multifactorial. Features that would characterize asthma patients at risk of NFA have been difficult to define but have included psychosocial barriers. environmental exposures, inadequate or inappropriate physician and/or patient responses to deteriorating asthma and, in particular, overreliance on symptomatic bronchodilator therapy. The association between fatal asthma and NFA with beta-agonist use has been controversial, with it being argued that high use of beta-agonists reflects severity of asthma as opposed to being causal. Studies in the laboratory and ambulatory care setting suggest that regular compared with as-required use of beta-agonists is associated with worsening in asthma control. Although a reduced perception of dyspnea has been identified in some asthma patients, it is not universally present in those with NFA. Retrospective data suggest that hyperinflation of the thorax, as judged by total lung capacity, may be a useful marker for subjects at risk of NFA. Future studies should better characterize these risk factors and develop management strategies (both therapeutic and educational) that might reduce the risk of subjects experiencing episodes of NFA and, by extension, reducing the continued unacceptable mortality associated with asthma.

2010 ◽  
Vol 47 (4) ◽  
pp. 460-464 ◽  
Author(s):  
Christopher L. Carroll ◽  
Burcin Uygungil ◽  
Aaron R. Zucker ◽  
Craig M. Schramm

EP Europace ◽  
2021 ◽  
Vol 23 (Supplement_3) ◽  
Author(s):  
L Calo" ◽  
V Bianchi ◽  
D Ferraioli ◽  
L Santini ◽  
A Dello Russo ◽  
...  

Abstract Funding Acknowledgements Type of funding sources: None. Introduction The HeartLogic algorithm combines multiple implantable cardioverter defibrillator (ICD) sensors to identify patients at risk of heart failure (HF) events. Purpose We sought to evaluate the risk stratification ability of this algorithm in clinical practice. We also analyzed the alert management strategies adopted in the study group and their association with the occurrence of HF events. Methods The HeartLogic feature was activated in 366 ICD and cardiac resynchronization therapy ICD patients at 22 centers. The HeartLogic algorithm automatically calculates a daily HF index and identifies periods IN or OUT of an alert state on the basis of a configurable threshold (in this analysis set to 16). Results The HeartLogic index crossed the threshold value 273 times (0.76 alerts/patient-year) in 150 patients over a median follow-up of 11 months [25-75 percentile: 6-16]. Overall, the time IN the alert state was 11% of the total observation period. Patients experienced 36 HF hospitalizations and 8 patients died of HF (rate: 0.12 events/patient-year) during the observation period. Thirty-five events were associated with the IN alert state (0.92 events/patient-year versus 0.03 events/patient-year in the OUT of alert state). The hazard ratio in the IN/OUT of alert state comparison was (HR: 24.53, 95% CI: 8.55-70.38, p < 0.001), after adjustment for baseline clinical confounders. Alerts followed by clinical actions were associated with a lower rate of HF events (HR: 0.37, 95% CI: 0.14-0.99, p = 0.047). No differences in event rates were observed between in-office and remote alert management. By contrast, verification of HF symptoms during post-alert examination was associated with a higher risk of HF events (HR: 5.23, 95% CI: 1.98-13.83, p < 0.001). Conclusions This multiparametric ICD algorithm identifies patients during periods of significantly increased risk of HF events. The rate of HF events seemed lower when clinical actions were undertaken in response to alerts. Extra in-office visits did not seem to be required in order to effectively manage HeartLogic alerts, while post-alert verification of symptoms seemed useful in order to better stratify patients at risk of HF events.


1996 ◽  
Vol 3 (4) ◽  
pp. 261-268 ◽  
Author(s):  
Malcolm R Sears

Many markers of asthma morbidity have shown substantial increases over the past two decades, including family physician visits, use of anti-asthma medications, emergency room visits and hospital admissions. The reported prevalence of diagnosed asthma and of wheezing has increased, especially in children, with accompanying evidence of increased atopy and increased airway responsiveness. Allergen exposure and parental smoking are significant risk factors for childhood wheezing, whereas the influence of outdoor air pollution is uncertain. Increasing use of beta-agonist treatment, which appears to increase the severity of asthma by increasing early and late responses to allergen, may contribute to increased morbidity and mortality, especially if potent beta-agonists are used. Risk factors for asthma mortality include age, smoking, allergy and airway lability, as well as over-reliance on beta-agonists and poor compliance with other aspects of treatment. Following withdrawal of the potent beta-agonist fenoterol in New Zealand, both hospital admissions and mortality from asthma fell abruptly. Continued patient and physician education, with emphasis on avoidance of risk factors and use of appropriate treatment, should reduce morbidity and mortality from asthma in Canada.


2005 ◽  
Vol 46 (5) ◽  
pp. 459-465 ◽  
Author(s):  
ESTHER ROMERO-FRAIS ◽  
MARIA ISABEL VAZQUEZ ◽  
EVA SANDEZ ◽  
MARINA BLANCO-APARICIO ◽  
ISABEL OTERO ◽  
...  

2005 ◽  
Vol 12 (2) ◽  
pp. 175-184 ◽  
Author(s):  
Eva Sández ◽  
María I. Vázquez ◽  
Esther Romero-Frais ◽  
Marina Blanco-Aparicio ◽  
Isabel Otero ◽  
...  

1995 ◽  
Vol 2 (1) ◽  
pp. 34-39 ◽  
Author(s):  
Pierre Ernst ◽  
Brenda Hemmelgarn ◽  
Donald W Cockcroft ◽  
Samy Suissa

OBJECTIVE: To assess the potential impact on the risk of life-threatening asthma of current recommendations in pharmacotherapy, which emphasize the early use of steroids and the avoidance of beta-agonist overuse.DESIGN: Nested case-control study.SETTING: Province of Saskatchewan.POPULATION STUDIED: From a cohort of 12,301 subjects dispensed 10 or more asthma medications from 1980 to 1987, 129 case patients were identified who had experienced an episode of fatal or near fatal asthma and 129 control patients matched to the cases on age, time period at risk and severity of asthma (as judged by the need for hospitalization for asthma in the preceding two years).METHODS: Two clinicians reviewed the therapy these 258 subjects had been dispensed over the prior two-year period and classified their treatment as ‘incompatible’ or ‘compatible’ (at least partially compatible) with current pharmacotherapeutic guide lines. In addition to this classification a treatment evaluation score was also applied to each study subject. This score was based on the use of anti-inflammatory therapy (oral and inhaled) in conjunction with the regular use of bronchodilators, as well as the use of oral corticosteroids for patients recently discharged from hospital foll owing an attack or asthma.RESULTS: At least one of the two clinician reviewers judged therapy to be incompatible with current standards in 49% of the case patients compared with 20% of the subjects who had not experienced a life-threatening episode. The mean ± SD treatment score was 3.5±1.7 in cases compared with 0.8±1.4 in controls, suggesting quality or pharmacological treatment was worse in cases (P<0.001).CONCLUSIONS: Pharmacological therapy incompatible with current recommendations was more common among cases of fatal and near fata l asthma in Saskatchewan from 1980 to 1987.


1995 ◽  
Vol 2 (suppl a) ◽  
pp. 32A-34A
Author(s):  
Pierre Ernst

The reported links of asthma morbidity and mortality to the use of in haled beta-agonist bronchodilators are reviewed. Reports from the Saskatchewan Asthma Epidemiology Project (SAEP) suggest that it is excessive use that is linked to life-threatening asthma and that patients at highest risk can be identified by their increasing use of these medications. This is the major justification for prescribing short acting beta-agonists on an as needed basis, though there is both clinical and experimental evidence suggesting regular use of these agents may not be beneficial. New longer acting inhaled beta-agonists designed for regular use are being introduced and their exact role remains to be defined. Provisionally, they appear to be useful in patients whose asthma is not well controlled with optimal doses of inhaled corticosteroids. The use of these newer agents for the relief of acute bronchospasm is contraindicated because of their slow onset of action.


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