User Experience of Self-Reported Computerized Medical History Taking for Acute Chest Pain in the Clinical Expert Operating System - Chest Pain Danderyd Study (CLEOS-CPDS): Interview Study Among Patients (Preprint)

2021 ◽  
Author(s):  
Kay Sundberg ◽  
Athena Adeli ◽  
Helge Brandberg ◽  
Jonas Spaak ◽  
Sabine Koch ◽  
...  

BACKGROUND Chest pain is one of the most common complaints in emergency departments (EDs). The effectiveness of care for patients with chest pain requires that individual circumstances and the complexity of the patient's clinical issues are determined by medical history taking. The knowledge base for history taking and for interpreting the clinical significance of the information collected can be formalized by software to enable computerized history taking (CHT) directly from patients and subsequently reporting the findings promptly to physicians. The adoption of CHT in clinical practice depends, among other issues, on reactions and attitudes to the technology from patients and their belief that the technology will have benefits for their medical care. OBJECTIVE The objective of this study was to explore the user experience of the self-reported CHT program CLEOS (Clinical Expert Operating System) in the setting of patients attending an ED for acute chest pain. METHODS This qualitative interview study is part of the ongoing CLEOS-Chest Pain Danderyd Study (CLEOS-CPDS), at a cardiology ED. A subset (n=84) of the larger sample who had taken part in self-reported history taking by the CLEOS program during waiting times at the ED were contacted by telephone and n=54 (64%) accepted participation. An interview guide with open-ended questions developed for this study was used. The text was analyzed using conventional content analysis in a deductive way by using the headings in the interview guide. RESULTS Six categories emerged: Clinical context, Individual context, Time aspect, Acceptability of the program, Usability of the program, and Perceptions of usefulness in a clinical context. A majority of the patients thought CLEOS had worked well. Patients also appreciated the opportunities, of interacting with the program and contributing to information about their own health while waiting for care. The program was generally perceived as easy to use and that the questions were mostly seen as relevant and straight forward. Many patients were of the opinion, however, that too many questions were asked and sometimes they mentioned there was insufficient time for responding to them. Some had found it difficult to find the strength to answer all the questions due to their condition. CONCLUSIONS The patients’ experience of the CLEOS program at a cardiology ED reflects an overall positive attitude. The CLEOS program was by some perceived as extensive, although most found the program user-friendly. Despite the busy ED environment, patients were highly motivated and felt that the program would be helpful in leading to a correct diagnosis. These findings suggest an important role for patient-entered CHT programs such as CLEOS in the setting of an ED from the perspective of the patients. CLINICALTRIAL ClinicalTrials.gov NCT03439449

2020 ◽  
Author(s):  
Helge Brandberg ◽  
Carl Johan Sundberg ◽  
Jonas Spaak ◽  
Sabine Koch ◽  
David Zakim ◽  
...  

BACKGROUND Chest pain is one of the most common chief complaints in emergency departments (EDs). Collecting an adequate medical history is challenging but essential in order to use recommended risk scores such as the HEART score (based on history, electrocardiogram, age, risk factors, and troponin). Self-reported computerized history taking (CHT) is a novel method to collect structured medical history data directly from the patient through a digital device. CHT is rarely used in clinical practice, and there is a lack of evidence for utility in an acute setting. OBJECTIVE This substudy of the Clinical Expert Operating System Chest Pain Danderyd Study (CLEOS-CPDS) aimed to evaluate whether patients with acute chest pain can interact effectively with CHT in the ED. METHODS Prospective cohort study on self-reported medical histories collected from acute chest pain patients using a CHT program on a tablet. Clinically stable patients aged 18 years and older with a chief complaint of chest pain, fluency in Swedish, and a nondiagnostic electrocardiogram or serum markers for acute coronary syndrome were eligible for inclusion. Patients unable to carry out an interview with CHT (eg, inadequate eyesight, confusion or agitation) were excluded. Effectiveness was assessed as the proportion of patients completing the interview and the time required in order to collect a medical history sufficient for cardiovascular risk stratification according to HEART score. RESULTS During 2017-2018, 500 participants were consecutively enrolled. The age and sex distribution (mean 54.3, SD 17.0 years; 213/500, 42.6% women) was similar to that of the general chest pain population (mean 57.5, SD 19.2 years; 49.6% women). Common reasons for noninclusion were language issues (182/1000, 18.2%), fatigue (158/1000, 15.8%), and inability to use a tablet (152/1000, 15.2%). Sufficient data to calculate HEART score were collected in 70.4% (352/500) of the patients. Key modules for chief complaint, cardiovascular history, and respiratory history were completed by 408 (81.6%), 339 (67.8%), and 291 (58.2%) of the 500 participants, respectively, while 148 (29.6%) completed the entire interview (in all 14 modules). Factors associated with completeness were age 18-69 years (all key modules: <i>P</i>s&lt;.001), male sex (cardiovascular: <i>P</i>=.04), active workers (all key modules: <i>P</i>s&lt;.005), not arriving by ambulance (chief complaint: <i>P</i>=.03; cardiovascular: <i>P</i>=.045), and ongoing chest pain (complete interview: <i>P</i>=.002). The median time to collect HEART score data was 23 (IQR 18-31) minutes and to complete an interview was 64 (IQR 53-77) minutes. The main reasons for discontinuing the interview prior to completion (n=352) were discharge from the ED (101, 28.7%) and tiredness (95, 27.0%). CONCLUSIONS A majority of patients with acute chest pain can interact effectively with CHT on a tablet in the ED to provide sufficient data for risk stratification with a well-established risk score. The utility was somewhat lower in patients 70 years and older, in patients arriving by ambulance, and in patients without ongoing chest pain. Further studies are warranted to assess whether CHT can contribute to improved management and prognosis in this large patient group. CLINICALTRIAL ClinicalTrials.gov NCT03439449; https://clinicaltrials.gov/ct2/show/NCT03439449 INTERNATIONAL REGISTERED REPORT RR2-10.1136/bmjopen-2019-031871


10.2196/25493 ◽  
2021 ◽  
Vol 23 (4) ◽  
pp. e25493
Author(s):  
Helge Brandberg ◽  
Carl Johan Sundberg ◽  
Jonas Spaak ◽  
Sabine Koch ◽  
David Zakim ◽  
...  

Background Chest pain is one of the most common chief complaints in emergency departments (EDs). Collecting an adequate medical history is challenging but essential in order to use recommended risk scores such as the HEART score (based on history, electrocardiogram, age, risk factors, and troponin). Self-reported computerized history taking (CHT) is a novel method to collect structured medical history data directly from the patient through a digital device. CHT is rarely used in clinical practice, and there is a lack of evidence for utility in an acute setting. Objective This substudy of the Clinical Expert Operating System Chest Pain Danderyd Study (CLEOS-CPDS) aimed to evaluate whether patients with acute chest pain can interact effectively with CHT in the ED. Methods Prospective cohort study on self-reported medical histories collected from acute chest pain patients using a CHT program on a tablet. Clinically stable patients aged 18 years and older with a chief complaint of chest pain, fluency in Swedish, and a nondiagnostic electrocardiogram or serum markers for acute coronary syndrome were eligible for inclusion. Patients unable to carry out an interview with CHT (eg, inadequate eyesight, confusion or agitation) were excluded. Effectiveness was assessed as the proportion of patients completing the interview and the time required in order to collect a medical history sufficient for cardiovascular risk stratification according to HEART score. Results During 2017-2018, 500 participants were consecutively enrolled. The age and sex distribution (mean 54.3, SD 17.0 years; 213/500, 42.6% women) was similar to that of the general chest pain population (mean 57.5, SD 19.2 years; 49.6% women). Common reasons for noninclusion were language issues (182/1000, 18.2%), fatigue (158/1000, 15.8%), and inability to use a tablet (152/1000, 15.2%). Sufficient data to calculate HEART score were collected in 70.4% (352/500) of the patients. Key modules for chief complaint, cardiovascular history, and respiratory history were completed by 408 (81.6%), 339 (67.8%), and 291 (58.2%) of the 500 participants, respectively, while 148 (29.6%) completed the entire interview (in all 14 modules). Factors associated with completeness were age 18-69 years (all key modules: Ps<.001), male sex (cardiovascular: P=.04), active workers (all key modules: Ps<.005), not arriving by ambulance (chief complaint: P=.03; cardiovascular: P=.045), and ongoing chest pain (complete interview: P=.002). The median time to collect HEART score data was 23 (IQR 18-31) minutes and to complete an interview was 64 (IQR 53-77) minutes. The main reasons for discontinuing the interview prior to completion (n=352) were discharge from the ED (101, 28.7%) and tiredness (95, 27.0%). Conclusions A majority of patients with acute chest pain can interact effectively with CHT on a tablet in the ED to provide sufficient data for risk stratification with a well-established risk score. The utility was somewhat lower in patients 70 years and older, in patients arriving by ambulance, and in patients without ongoing chest pain. Further studies are warranted to assess whether CHT can contribute to improved management and prognosis in this large patient group. Trial Registration ClinicalTrials.gov NCT03439449; https://clinicaltrials.gov/ct2/show/NCT03439449 International Registered Report Identifier (IRRID) RR2-10.1136/bmjopen-2019-031871


2004 ◽  
Vol 116 (3) ◽  
pp. 83-89 ◽  
Author(s):  
Martin Schillinger ◽  
Gottfried Sodeck ◽  
Giora Meron ◽  
Karin Janata ◽  
Mariam Nikfardjam ◽  
...  

Author(s):  
Christine Arnold ◽  
Sarah Berger ◽  
Nadine Gronewold ◽  
Denise Schwabe ◽  
Burkhard Götsch ◽  
...  

2017 ◽  
Vol 18 (6) ◽  
pp. 403-408 ◽  
Author(s):  
Aya Matsushita ◽  
Junji Haruta ◽  
Madoka Tsutumi ◽  
Takuya Sato ◽  
Tetsuhiro Maeno

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