Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Hideko Kidokoro is active.

Publication


Featured researches published by Hideko Kidokoro.


Journal of Gastroenterology and Hepatology | 2009

Effects of terlipressin on systemic, hepatic and renal hemodynamics in patients with cirrhosis

Yoshiyuki Narahara; Hidenori Kanazawa; Yasuhiko Taki; Yuu Kimura; Masanori Atsukawa; Tamaki Katakura; Hideko Kidokoro; Hirotomo Harimoto; Takeshi Fukuda; Yoko Matsushita; Katsuhisa Nakatsuka; Choitsu Sakamoto

Background and Aim:  Terlipressin has been shown to be effective in the management of hepatorenal syndrome. However, how terlipressin exerts its effect on the renal artery is unknown. The aim of the present study was to assess the effects of terlipressin on systemic, hepatic and renal hemodynamics in cirrhosis.


Journal of Viral Hepatitis | 2012

An open-label randomized controlled study of pegylated interferon/ribavirin combination therapy for chronic hepatitis C with versus without fluvastatin.

Chisa Kondo; Masanori Atsukawa; Akihito Tsubota; Norio Itokawa; Takeshi Fukuda; Yoko Matsushita; Hideko Kidokoro; Tamaki Kobayashi; Yoshiyuki Narahara; Katsuhisa Nakatsuka; Hidenori Kanazawa; Choitsu Sakamoto

Summary.  Pegylated interferon (PEG‐IFN)/ribavirin combination therapy is the standard‐of‐care (SOC) treatment for chronic hepatitis C patients infected with hepatitis C virus (HCV) genotype 1b and high viral load. The addition of fluvastatin to SOC treatment has been suggested to be effective for better outcome in retrospective pilot analyses. We investigated whether the combination of fluvastatin with PEG‐IFN/ribavirin could actually improve sustained viral response (SVR) in patients with HCV genotype 1b and high viral load. A randomized, open‐labeled, controlled study was conducted between July 2008 and December 2009 in 101 chronic hepatitis C patients allocated to PEG‐IFN/ribavirin combination therapy with or without fluvastatin. SVR rates were calculated in groups, stratifying host and viral factors. We also analyzed predictive factors for SVR among patients on fluvastatin with multivariate regression analysis. Rapid and early virological, and end of treatment response rates in the fluvastatin group were not significantly different from those in the non‐fluvastatin group. Notwithstanding, SVR rate was significantly higher in the fluvastatin group than in the non‐fluvastatin group (63.0%vs 41.7%, P = 0.0422). Comparison of the two groups stratifying demographic data and HCV characteristics showed significantly higher SVR rates to more than 80% in males, more than two mutations in the interferon sensitivity determining region (ISDR), and a history of relapse among the fluvastatin group than the non‐fluvastatin group. Being male and major genotype IL28B single nucleotide polymorphisms (SNPs) were independent predictive factors for SVR among patients on fluvastatin with multivariate analysis. Fluvastatin‐combined with PEG‐IFN/ribavirin therapy significantly improves SVR rates in patients with HCV genotype 1b and high viral load. Male and major genotype IL28B SNPs were independent predictors for SVR among patients on fluvastatin combination therapy.


Journal of Gastroenterology and Hepatology | 2013

Combination of fluvastatin with pegylated interferon/ribavirin therapy reduces viral relapse in chronic hepatitis C infected with HCV genotype 1b

Masanori Atsukawa; Akihito Tsubota; Chisa Kondo; Norio Itokawa; Yoshiyuki Narahara; Katsuhisa Nakatsuka; Satomi Hashimoto; Takeshi Fukuda; Yoko Matsushita; Hideko Kidokoro; Tamaki Kobayashi; Hidenori Kanazawa; Choitsu Sakamoto

Although the anti‐hepatitis C virus (HCV) effect of statins in vitro and clinical efficacy of fluvastatin combined with Pegylated interferon (PEG‐IFN)/ribavirin therapy for chronic hepatitis C (CHC) have been reported, the details of clinical presentation are largely unknown. We focused on viral relapse that influences treatment outcome, and performed a post‐hoc analysis by using data from a randomized controlled trial.


Hepatitis Monthly | 2013

EFFICACY OF ALFACALCIDOL ON PEG-IFN/ RIBAVIRIN COMBINATION THERAPY FOR ELDERLY PATIENTS WITH CHRONIC HEPATITIS C: A PILOT STUDY

Masanori Atsukawa; Akihito Tsubota; Noritomo Shimada; Chisa Kondo; Norio Itokawa; Ai Nakagawa; Satomi Hashimoto; Takeshi Fukuda; Yoko Matsushita; Hideko Kidokoro; Yoshiyuki Narahara; Katsuhisa Nakatsuka; Katsuhiko Iwakiri; Chiaki Kawamoto; Choitsu Sakamoto

Background Serum vitamin D concentration is reported to show a decrease in older age. Patients with chronic hepatitis C (CHC) in Japan are older on average than those in Western countries. Moreover, the outcome of pegylated-interferon (PEG-IFN)/ ribavirin therapy combined with vitamin D in elderly patients is unclear. Objectives This pilot study explored the efficacy and safety of alfacalcidol as vitamin D source in PEG-IFN/ ribavirin combination therapy for elderly CHC patients infected with hepatitis C virus genotype 1b. Patients and Methods Consecutive twenty CHC patients aged ≥ 65 years were enrolled in this pilot study. Fifteen patients met the inclusion criteria and received PEG-IFN/ ribavirin therapy combined with alfacalcidol. Four-week lead-in of oral alfacalcidol was conducted, and it was subsequently and concurrently administered in PEG-IFN/ ribavirin combination therapy (vitamin D group). Age, gender, and IL28B genotype-matched patients, who received PEG-IFN/ ribavirin alone, were saved as control group (n = 15) to compare the treatment outcome with the vitamin D group. Results Subjects consisted of 14 males and 16 females, with a median age of 70 years (65-78). The serum 25 (OH) D3 concentration in females (20 ng/ml, 11-37) was significantly lower than males (27 ng/mL, 13-49) (P = 0.004). Sustained virological response (SVR) rates were 33.3% (5/15) in the control group and 80.0% (12/15) in the vitamin D group, respectively (P = 0.025). While no significant difference was shown in the (SVR) rate between the two groups among males (P = 0.592), in females the SVR rate was significantly higher in the vitamin D group (87.5%, 7/8) than the control group (25.0%, 2/8) (P = 0.041). The relapse rates in the groups with and without alfacalcidol were 7.7% (1/13) and 61.5% (8/13), respectively (P = 0.011). Interestingly, in females, the relapse in the control group was shown in 5 of 7 (71.4%), whereas in the vitamin D group the relapse rate was decreased (1/8, 12.5%) (P = 0.041). No specific adverse events were observed in the vitamin D group. Conclusions PEG-IFN/ ribavirin combined with alfacalcidol may be effective and safe in elderly CHC patients. In particular, concomitant administration of alfacalcidol may lead to a reduced relapse rate, and consequently improving the SVR rate in elderly females.


Hepatology Research | 2014

Predictive factors for improvement of ascites after transjugular intrahepatic portosystemic shunt in patients with refractory ascites

Yasuhiko Taki; Hidenori Kanazawa; Yoshiyuki Narahara; Norio Itokawa; Chisa Kondo; Takeshi Fukuda; Hirotomo Harimto; Yoko Matsushita; Hideko Kidokoro; Tamaki Katakura; Masanori Atsukawa; Yuu Kimura; Katsuhisa Nakatsuka; Choitsu Sakamoto

The aim of this study was to investigate the predictive factors for the response of ascites to a transjugular intrahepatic portosystemic shunt (TIPS) and the impact of improvement of ascites on the overall prognosis of patients with cirrhosis and refractory ascites.


Journal of Gastroenterology and Hepatology | 2014

Effects of fasudil on the portal and systemic hemodynamics of patients with cirrhosis.

Takeshi Fukuda; Yoshiyuki Narahara; Hidenori Kanazawa; Yoko Matsushita; Hideko Kidokoro; Norio Itokawa; Chisa Kondo; Masanori Atsukawa; Katsuhisa Nakatsuka; Choitsu Sakamoto

Fasudil, a Rho‐kinase inhibitor, has been shown to reduce portal venous pressure in cirrhotic rats. However, its effects on portal and systemic hemodynamics have not been investigated in cirrhotic patients with portal hypertension. The aim of this study was to assess the effects of fasudil on the portal and systemic hemodynamics of cirrhotic patients with portal hypertension.


Journal of Gastroenterology and Hepatology | 2013

Lead-in treatment with interferon-β/ribavirin may modify the early hepatitis C virus dynamics in pegylated interferon alpha-2b/ribavirin combination for chronic hepatitis C patients with the IL28B minor genotype

Norio Itokawa; Masanori Atsukawa; Akihito Tsubota; Chisa Kondo; Satomi Hashimoto; Takeshi Fukuda; Yoko Matsushita; Hideko Kidokoro; Tamaki Kobayashi; Yoshiyuki Narahara; Katsuhisa Nakatsuka; Hidenori Kanazawa; Katsuhiko Iwakiri; Choitsu Sakamoto

The most important factor influencing the effect of pegylated interferon (PEG‐IFN)/ribavirin therapy (PEG) for chronic hepatitis C genotype 1b with high viral load is the interleukin 28B (IL28B) genotype. We investigated the usefulness of lead‐in twice‐daily interferon (IFN)‐β/ribavirin therapy (IFN‐β), and the early hepatitis C virus RNA (HCV‐RNA) dynamics was compared between PEG and IFN‐β groups according to the IL28B genotype.


Journal of Gastroenterology | 2011

Transjugular intrahepatic portosystemic shunt versus paracentesis plus albumin in patients with refractory ascites who have good hepatic and renal function: a prospective randomized trial

Yoshiyuki Narahara; Hidenori Kanazawa; Takeshi Fukuda; Yoko Matsushita; Hirotomo Harimoto; Hideko Kidokoro; Tamaki Katakura; Masanori Atsukawa; Yasuhiko Taki; Yuu Kimura; Katsuhisa Nakatsuka; Choitsu Sakamoto


Journal of Gastroenterology | 2013

Effects of transjugular intrahepatic portosystemic shunt on changes in the small bowel mucosa of cirrhotic patients with portal hypertension

Yoko Matsushita; Yoshiyuki Narahara; Shunji Fujimori; Hidenori Kanazawa; Norio Itokawa; Takeshi Fukuda; Yoko Takahashi; Chisa Kondo; Hideko Kidokoro; Masanori Atsukawa; Katsuhisa Nakatsuka; Choitsu Sakamoto


Clinical Journal of Gastroenterology | 2011

A case of IgG4-related disease with rectal cancer

Norio Itokawa; Masanori Atsukawa; Takayoshi Nishino; Chisa Kondo; Takeshi Fukuda; Yoko Matsushita; Hideko Kidokoro; Tamaki Katakura; Yoshiyuki Narahara; Shu Tanaka; Katsuhisa Nakatsuka; Yoshiharu Oaki; Choitsu Sakamoto

Collaboration


Dive into the Hideko Kidokoro's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Akihito Tsubota

Jikei University School of Medicine

View shared research outputs
Researchain Logo
Decentralizing Knowledge