TY - JOUR
T1 - Clinical features of adult patients with Eisenmenger's syndrome in Japan and Korea
AU - Sakazaki, Hisanori
AU - Niwa, Koichiro
AU - Nakazawa, Makoto
AU - Saji, Tsutomu
AU - Nakanishi, Toshio
AU - Takamuro, Motoki
AU - Ueno, Michihiko
AU - Kato, Hitoshi
AU - Takatsuki, Shinichi
AU - Matsushima, Masaki
AU - Kojima, Namiko
AU - Ichida, Fukiko
AU - Kogaki, Shigetoyo
AU - Kido, Sachiko
AU - Arakaki, Yoshio
AU - Waki, Kenji
AU - Akagi, Teiji
AU - Joo, Kunitaka
AU - Muneuchi, Jun
AU - Suda, Kenji
AU - Lee, Heung Jae
AU - Shintaku, Haruo
PY - 2013/7/15
Y1 - 2013/7/15
N2 - Background: There are few articles on mortality and morbidity of adult patients with Eisenmenger's syndrome (ES) in the current era when disease targeting therapy (DTT) has been available. Methods and results: 198 patients (a median age 35 years, 64% female) with ES who visited the 16 participating institutes in Japan and Korea from 1998 to 2009 were enrolled. Clinical data during adulthood were collected from each institutional chart and analyzed centrally. During a median follow-up of 8 years, 30 patients died including 14 sudden deaths. 89 patients took oral medication of DTT and clinical improvement was observed in 54 of them. However, survival rate in patients taking DTT was not different from those without (87% vs 84%, p = 0.55). When the clinical data in between first and last clinic visits were compared in 85 patients, the patients with NYHA ≧ III increased from 24% to 48% (p < 0.001), SpO2 decreased from 89% to 85% (p = 0.008) and hematocrit increased from 51.4% to 52.9% (p = 0.04). Non-survivors had poorer NYHA function class, lower body weight (BW), lower body mass index (BMI), and higher serum level of Cr at the first visits than survivors. Conclusions: Long term survival and clinical status of adult patients with ES remains unsatisfactory even in the current era of DTT. Poor NYHA functional class, low BW, low BMI and high serum level of Cr were related to mortality. DTT therapy improved clinical status in many patients with Eisenmenger's syndrome, but no significant impact on survival could be shown.
AB - Background: There are few articles on mortality and morbidity of adult patients with Eisenmenger's syndrome (ES) in the current era when disease targeting therapy (DTT) has been available. Methods and results: 198 patients (a median age 35 years, 64% female) with ES who visited the 16 participating institutes in Japan and Korea from 1998 to 2009 were enrolled. Clinical data during adulthood were collected from each institutional chart and analyzed centrally. During a median follow-up of 8 years, 30 patients died including 14 sudden deaths. 89 patients took oral medication of DTT and clinical improvement was observed in 54 of them. However, survival rate in patients taking DTT was not different from those without (87% vs 84%, p = 0.55). When the clinical data in between first and last clinic visits were compared in 85 patients, the patients with NYHA ≧ III increased from 24% to 48% (p < 0.001), SpO2 decreased from 89% to 85% (p = 0.008) and hematocrit increased from 51.4% to 52.9% (p = 0.04). Non-survivors had poorer NYHA function class, lower body weight (BW), lower body mass index (BMI), and higher serum level of Cr at the first visits than survivors. Conclusions: Long term survival and clinical status of adult patients with ES remains unsatisfactory even in the current era of DTT. Poor NYHA functional class, low BW, low BMI and high serum level of Cr were related to mortality. DTT therapy improved clinical status in many patients with Eisenmenger's syndrome, but no significant impact on survival could be shown.
KW - Congenital heart disease
KW - Eisenmenger's syndrome
KW - Hypoxemia
KW - Pulmonary hypertension
KW - Pulmonary vasodilator
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U2 - 10.1016/j.ijcard.2011.12.030
DO - 10.1016/j.ijcard.2011.12.030
M3 - Article
C2 - 22227251
AN - SCOPUS:84878593007
SN - 0167-5273
VL - 167
SP - 205
EP - 209
JO - International Journal of Cardiology
JF - International Journal of Cardiology
IS - 1
ER -