Participants
In Japan, all residents have to complete a 2-year post-graduate residency in their primary subject, with rotations in other departments, such as internal medicine, surgery, emergency medicine, or anesthesia. The residents are also required to receive training for at least 3 months in the department of emergency or in the department of emergency and anesthesiology at their medical institute (15) within 2 years after graduating from a medical school. First- and second-year residents at Chiba University Hospital participated in our educational program in March 2022. All the participants had undergone training in the Department of Emergency Medicine and were in charge of patients requiring MV.
Ethical approval
This study was approved by the Ethics Committee of Chiba University (approval no. 4106). The study database was anonymized, and the study complied with the requirements of the Japanese Ministry of Health, Labour and Welfare. Informed consent was obtained from all participants when they answered the pre-seminar and post-seminar survey. All methods were performed in accordance with relevant guidelines and regulations.
Educational program
For efficient learning, flipped classrooms were used, wherein e-learning was implemented first, followed by hands-on training. The 2-hour educational program consisted of three sections: e-learning, hands-on training with a lung simulator (TTLTM Model Lung, Michigan Instruments, Talon Court SE, MI, USA), and hands-on training with a human patient simulator (SimMan 3GTM, Laerdal Medical, Tanke Svilandsgate, Stavanger, Norway). The content of the program was based on the main findings of focus group interviews (FGIs) with respiratory physicians at our hospital. The semi-structured FGIs regarding the development of a new educational strategy for MV management were performed. FGIs were conducted by a physician researcher (HK), and the interview responses were recorded independently using an interview guide. Respiratory physicians were asked the following questions: (1) What difficulties have you experienced with respect to MV management? (2) What knowledge and abilities are necessary for proper MV management? (3) What knowledge and abilities do you lack to properly perform MV management? (4) What learning opportunities about MV management would you find useful? The interview guide was validated by the two researchers (HK and HT) before data collection. As a results, learning respiratory physiology was necessary and the program should be based on experientially learning. In addition, the following learning goal was set: to be capable of providing basic respiratory care during an outbreak of a respiratory infection. Furthermore, this program was endorsed by a respiratory medicine specialist (HK), critical care specialist (TI), and medical education specialist (SI).
E-learning for respiratory physiology and MV
The aim of the e-learning module was to impart knowledge on respiratory care, including MV. The 30-minute online module included lectures on respiratory physiology and MV, namely indications, introduction, troubleshooting, and weaning. The participants watched the e-learning videos which consist of descriptions with audio and slides before starting the simulation-based training.
Hands-on training with a lung simulator
The aim of the training with a lung simulator was to help the participants to learn about manual ventilation and MV techniques, to experientially learn (using visual and tactile stimuli) and understand the changes in lung compliance and airway resistance during manual and MV, and to be able to apply these changes to their ventilator settings. This activity also helped the participants apply the knowledge learned from the e-lectures. The session was conducted under the supervision of two respiratory physicians (KT, HK) and lasted approximately 45 minutes. For this activity, a lung simulator (TTLTM Model Lung) was connected to a Jackson Rees circuit and ventilator (Evita V500TM, Dräger, Moislinger Allee, Lübeck, Germany) (Figures 1-A, B).
Hands-on training with a human patient simulator
The aim of the training with a human patient simulator was to help the participants obtain practical experience in assessing respiratory status and introducing MV. The simulation was conducted under the supervision of an intensivist (TI) and clinical engineer (YF). Severe respiratory failure due to infectious pneumonia was simulated using a human patient simulator (SimMan 3GTM) that was connected to a breathing simulator (ASL 5000TM, IngMar Medical, Pittsburgh, PA, USA). The learning activity was performed by teams of five-to-six participants at a time; they learned the process of MV administration, which included assessing the respiratory status, beginning manual ventilation, intubating, and adjusting the MV settings (Figures 1-C).
Evaluation of the effectiveness of the educational program
Questionnaire survey
Quantitative data were collected using questionnaires to evaluate the effectiveness of the education program on MV management. The questionnaire was designed to assess the participants’ motivation to learn about MV and the psychological burden of respiratory care required by patients requiring MV management. Their understanding of terminologies related to MV management was also assessed. Before and after the e-learning and hands-on training, the residents responded to the following questionnaire items (Table 1): (1a) How motivated do you feel to learn about MV? (1b) How much psychological burden of providing respiratory care to patients requiring MV management do you feel? (1c) What do you find difficult about MV? (2) How well do you understand the terminologies below? a. fraction of inspiratory oxygen (FIO2), b. positive end-expiratory pressure (PEEP), c. pressure support, d. continuous positive airway pressure (CPAP), e. assist/control (A/C), f. airway pressure, g. tidal volume, and h. end tidal CO2 (ETCO2).
Questions (1a) and (1b) were scored on a five-point Likert scale, with scores ranging from 1 (1a, very weak; 1b, very uncomfortable) to 5 (1a, very strong; 1b, very comfortable). Question (2) was scored on a four-point rating scale: 1 (I have never heard it), 2 (I have simply heard it), 3 (I know it but cannot explain it), and 4 (I can explain it). In addition, the participants reported their satisfaction level with the e-learning and hands-on training in a different questionnaire.
Multiple-choice questions (MCQs)
The participants answered six MCQs on the evaluation of blood gas analysis, indications for MV, selection of MV mode depending on the patient’s condition, method to modify hypoxemia/hypercapnia during MV, and weaning patients from MV. The MCQs were designed under the supervision of a respiratory medicine specialist (HK) and medical education specialist (SI).
Data analysis
Statistical analysis
Quantitative data were expressed as mean ± standard deviation (SD), unless otherwise indicated. The Wilcoxon signed-rank test was used to compare the degree of psychological burden before and after MV education. A p-value <0.05 was considered statistically significant. All statistical analyses were performed using JMP 15.0 (Cary, North Carolina, USA).