Masahiro Sogabe

Prof. Dr. Masahiro Sogabe


Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 July 2016 in Clinical Journal of Gastroenterology
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Journal Article
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MSMasahiro Sogabe
Masahiro Sogabe
TOToshiya Okahisa
Toshiya Okahisa
TKTetsuo Kimura
Tetsuo Kimura
KOKoichi Okamoto
Koichi Okamoto
HMHiroshi Miyamoto
Hiroshi Miyamoto
TTTetsuji Takayama
Tetsuji Takayama

8 July 2005 in Journal of Gastroenterology
Verified
Journal Article
Closed access
PDF file
MSMasahiro Sogabe
Masahiro Sogabe
TOToshiya Okahisa
Toshiya Okahisa
KTKoji Tsujigami
Koji Tsujigami
YOYoshio Okita
Yoshio Okita
HHHiroshige Hayashi
Hiroshige Hayashi
SISusumu Ito
Susumu Ito

9 November 2011 in Journal of Gastroenterology
Verified
Journal Article
Closed access
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MSMasahiro Sogabe
Masahiro Sogabe
TOToshiya Okahisa
Toshiya Okahisa
SHShingo Hibino
Shingo Hibino
AYAkira Yamanoi
Akira Yamanoi

29 August 2018 in BMC Gastroenterology
Verified
Journal Article
Open access
PDF file
MSMasahiro Sogabe
Masahiro Sogabe
TOToshiya Okahisa
Toshiya Okahisa
YAYuka Adachi
Yuka Adachi
MTMasanori Takehara
Masanori Takehara
SHShinichi Hamada
Shinichi Hamada
TTTetsuji Takayama
Tetsuji Takayama
Although many patients still have anxiety about upper gastrointestinal (GI) endoscopy, there have been few reports on the influence of distractions for a person who is going to undergo upper GI endoscopy soon. This study was a prospective randomized controlled study investigating the influence of distractions, such as auditive and visual distractions using subjective and objective assessments including autonomic nervous function prior to upper GI endoscopy. 206 subjects who underwent upper GI endoscopy as regular health check-ups were divided randomly into 4 groups prior to upper GI endoscopy; group 1 (control group), group 2 (auditive group), group 3 (visual group), and group 4 (combination group). We measured vital signs, autonomic nervous function, profile of mood state (POMS), and the impression for upper GI endoscopy pre- and post-distraction in the 4 groups. There was no significant difference in vital signs between 5 and 15 min after sitting in group 1, however, several vital signs in all distraction groups improved significantly after distraction (Pulse rate (P): p < 0.001 in group 4; blood pressure: p < 0.05 in group 2, 3, 4) and the rate of decrease in P and diastolic blood pressure was highest in group 4 (p < 0.001). Several scores of POMS and the impression for upper GI endoscopy post-distraction improved significantly compared to pre-distraction between distraction groups and the satisfaction for distraction was highest in group 4 (p < 0.01). Regarding autonomic nerve function, the low- frequency power/ high- frequency power ratio post-distraction was significantly lower than that pre-distraction in all distraction groups (p < 0.001). Although auditive distraction alone and visual distraction alone were effective, a combination distraction was more effective than any other distraction by subjective and objective assessments. These distractions, which were simple and safe, may play an assistive role in the stability of physical and psychological conditions prior to upper GI endoscopy. This trial was registered in the University Hospital Medical Information Network (UMIN) Clinical Trials Registry as UMIN000022801 . Registered on 10 July 2016.

26 April 2013 in Hepatology Research
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Journal Article
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MSMasahiro Sogabe
Masahiro Sogabe
TOToshiya Okahisa
Toshiya Okahisa
KTKoji Tsujigami
Koji Tsujigami
HFHiroshi Fukuno
Hiroshi Fukuno
SHShingo Hibino
Shingo Hibino
AYAkira Yamanoi
Akira Yamanoi

21 April 2020 in BMC Gastroenterology
Verified
Journal Article
Open access
PDF file
MSMasahiro Sogabe
Masahiro Sogabe
TOToshiya Okahisa
Toshiya Okahisa
AFAkira Fukuya
Akira Fukuya
KKKaizo Kagemoto
Kaizo Kagemoto
YOYasuyuki Okada
Yasuyuki Okada
TTTetsuji Takayama
Tetsuji Takayama
Esophagogastroduodenoscopy (EGD) provides an indispensable and unambiguous inspection allowing the discovery upper gastrointestinal lesions. However, many patients are anxious about undergoing EGD. Few studies have investigated the influence on patients’ vital signs and tolerance during EGD using subjective and objective assessments. This study was a prospective randomized controlled study that investigated the influence of audio and visual distraction on EGD. We randomly divided 289 subjects who underwent EGD into 4 groups (control group, audio group, visual group, combination group) and examined their vital signs, heart rate variability (HRV), psychological items, and acceptance of distraction. Pulse rate (PR) at post-distraction and post-EGD in the 3 distraction groups were significantly lower than those of control group (p < 0.001 and p < 0.01, respectively). Blood pressure (BP) during and post-EGD was significantly higher than that at pre-EGD in control group (p < 0.05), but no significant elevation of BP was observed during the latter half of EGD and post-EGD in the 3 distraction groups. BP at post-distraction improved significantly compared to pre-distraction in the 3 distraction groups (p < 0.05). There was a significant difference in the low-frequency (LF) power/ high-frequency (HF) power at post-distraction and post-EGD among the 4 groups (p < 0.001 and p < 0.001, respectively). The LF power/HF power at post-distraction and post-EGD in the 3 distraction groups was significantly lower than that in control group (p < 0.05). Several items of profile of mood states (POMS) and the impression of EGD at post-distraction improved significantly compared to those at pre-distraction among the 3 distraction groups (p < 0.05). Visual analog scale (VAS) of willingness for the next use of distraction in the 3 distraction groups was excellent because VAS was more than 70. Distractions effectively improved psychological factors, vital signs and some of HRV at pre and post-EGD. Distractions may suppress BP elevation during the latter half of EGD and lead to stability of HRV on EGD. This prospective trial was registered in the University Hospital Medical Information Network (UMIN) Clinical Trials Registry as UMIN000029637. Registered on 20 October 2017.