scholarly journals Reliability of the ASA physical status scale in clinical practice: methodological issues

2015 ◽  
Vol 114 (1) ◽  
pp. 162-163 ◽  
Author(s):  
S. Sabour
1981 ◽  
Vol 12 (1) ◽  
pp. 35-38 ◽  
Author(s):  
Robert N. Butler

Historically, doctors have not entertained a broad enough view of the total human life cycle. While much attention has been focused on infancy, childhood, adolescence and adulthood as times of growth and change, we have all but ignored the later years and the often marvelous characteristics of “the survivors.” The use of standardized methods for evaluating the mental and physical status of old people has deprived both practitioners and patients of the richness of life-long experiences. By taking the time to attentively listen to their patients' reflections of the past, physicians can help advance our growing understanding of human aging and expand the repertoire of mechanisms that are useful in clinical practice.


1996 ◽  
Vol 20 (11) ◽  
pp. 676-680 ◽  
Author(s):  
Peter L. Cornwall ◽  
Fuad Hassanyeh ◽  
Caprice Horn

We audited the use of high-dose antipsychotic drugs in patients admitted to a special (intensive) care unit over two periods. Five out of 57 patients in the first sample and three out of 62 in the second were treated with a single antipsychotic drug above the British National Formulary maximum dose. The proportion of patients treated with antipsychotic drugs such that the total dose in chlorpromazine equivalents was greater than 1000 mg, fed. The audit showed improvements in clinical practice, particularly with respect to the onset of, indication for and outcome of high-dose treatment and in monitoring the patients' physical status.


2015 ◽  
Vol 59 (4) ◽  
pp. 202-203 ◽  
Author(s):  
A. Sankar ◽  
S. R. Johnson ◽  
W. S. Beattie ◽  
G. Tait ◽  
D. N. Wijeysundera

2017 ◽  
Vol 2017 ◽  
pp. 1-13 ◽  
Author(s):  
Erik W. Baars ◽  
Harald J. Hamre

Background. There is an increasing need for a worldwide professional integration of conventional medicine and traditional/complementary whole medical systems (WMSs). However, the integration is perceived by conventional medicine as problematic or unacceptable, because of a supposed lack of evidence for specific effects of WMSs therapies and supposed prescientific or unscientific paradigms of WMSs. Objectives. To review the literature on the features of WMSs, similarities and differences between conventional medicine and WMSs, and scientific and clinical practice issues that should be dealt with in order to promote the integration process. Methods. A critical, narrative review of the literature on six WMSs. Results and Conclusions. Key factors for the integration of WMSs and conventional medicine are as follows: legal frameworks, quality standards, high-quality research on safety and efficacy of WMS interventions, infrastructure, and financial resources. For scientific assessment of WMSs, there are unresolved ontological, epistemological, and methodological issues and issues of diagnostics, therapy delivery, and outcome assessment in clinical practice. Future research not only should be directed at quality assurance and generating the necessary data on safety and efficacy/effectiveness but also should address more fundamental (ontological, epistemological, and methodological) issues, in order to overcome the differences between WMSs and conventional medicine.


2020 ◽  
Author(s):  
Manon Ansart ◽  
Stephane Epelbaum ◽  
Giulia Bassignana ◽  
Alexandre Bone ◽  
Simona Bottani ◽  
...  

We performed a systematic review of studies focusing on the automatic prediction of the progression of mild cognitive impairment to Alzheimer's disease (AD) dementia, and a quantitative analysis of the methodological choices impacting performance. This review included 172 articles, from which 234 experiments were extracted. For each of them, we reported the used data set, the feature types, the algorithm type, performance and potential methodological issues. The impact of these characteristics on the performance was evaluated using a multivariate mixed effect linear regressions. We found that using cognitive, fluorodeoxyglucose-positron emission tomography or potentially electroencephalography and magnetoencephalography variables significantly improved predictive performance compared to not including them, whereas including other modalities, in particular T1 magnetic resonance imaging, did not show a significant effect. The good performance of cognitive assessments questions the wide use of imaging for predicting the progression to AD and advocates for exploring further fine domain-specific cognitive assessments. We also identified several methodological issues, including the absence of a test set, or its use for feature selection or parameter tuning in nearly a fourth of the papers. Other issues, found in 15% of the studies, cast doubts on the relevance of the method to clinical practice. We also highlight that short-term predictions are likely not to be better than predicting that subjects stay stable over time. These issues highlight the importance of adhering to good practices for the use of machine learning as a decision support system for the clinical practice.


2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Sara Patuzzo ◽  
Paolo Manganotti

The aim of the present paper was to investigate the fundamental ethical issues of Deep Brain Stimulation (DBS) on patients remaining in Persistent Vegetative State (PVS). First, the purpose of this analysis was to discuss the nature of this intervention in order to classify it such as an ordinary clinical practice, or otherwise as an extraordinary clinical practice or as experimental research. Second, ethical issues, criticisms, and methodological issues of this intervention, also in the future perspectives, are discussed, attempting to identify who could give informed consent for a patient in PVS.


2020 ◽  
Vol 3 ◽  
pp. 1-10 ◽  
Author(s):  
Jose Paulo Guida

Objective: to assess effectiveness and safety of hydroxychloroquine and chloroquine on the treatment of COVID-19. Study desing: a systematic review of literature was performed in two databases; studies were included if they had as intervention use of chloroquine or hydroxychloroquine and reported outcomes on laboratorial or clinical findings or description of side effects. Results: 38 studies were included; of those, only one fulfilled inclusion criteria and were included in this review. This study has important methodological issues and only reported viral load, but any clinical outcomes. Conclusions: Many ongoing clinical trials will provide new evidences about the use of hydroxychloroquine and chloroquine to the treatment of COVID-19. Current evidence do not support its use on clinical practice.


2014 ◽  
Vol 113 (3) ◽  
pp. 424-432 ◽  
Author(s):  
A. Sankar ◽  
S.R. Johnson ◽  
W.S. Beattie ◽  
G. Tait ◽  
D.N. Wijeysundera

2021 ◽  
Author(s):  
Zoltan Kekecs ◽  
Donald Moss ◽  
Gary Elkins ◽  
Giuseppe De Benedittis ◽  
Olafur Pallson ◽  
...  

The research on the efficacy of hypnosis applications continues to grow, yet there is frequently a chasm between scientific knowledge and clinical practice. One challenge has been a lack of a unified standard for efficacy research in hypnosis. In 2018, six major hypnosis organizations collaborated to form a Task Force for Establishing Efficacy Standards for Clinical Hypnosis. The present paper reports the Guidelines for the Assessment of Efficacy of Clinical Hypnosis Applications created by the Task Force listing ten specific recommendations. These recommendations are intended to guide researchers who want to assess the accumulated evidence in existing research about the efficacy of applications of clinical hypnosis. The paper also discusses methodological issues in the interpretation and implementation of these guidelines. Future papers will report on the other products of the Hypnosis Efficacy Task Force, such as best practice recommendations for outcomes research in hypnosis, and an international survey of researchers and clinicians on current practices and views of hypnosis.


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