TY - JOUR
T1 - Inhaled nitric oxide therapy after fontan-type operations
AU - Yoshimura, Naoki
AU - Yamaguchi, Masahiro
AU - Oka, Shigeteru
AU - Yoshida, Masahiro
AU - Murakami, Hirohisa
AU - Kagawa, Tetsuro
AU - Suzuki, Takeshi
PY - 2005
Y1 - 2005
N2 - Purpose. Inhaled nitric oxide (NO) therapy is a newly developed strategy designed to reduce pulmonary vascular resistance after the Fontan-type operation. We reviewed our experience to evaluate its efficacy and true indications. Methods. We retrospectively examined 47 children who received inhaled NO therapy after the Fontan-type operation between August 1996 and December 2002. The maximal dose of NO ranged from 5 to 30ppm (median 10ppm), and the duration of inhaled NO therapy ranged from 5h to 52 days (median 2 days). Results. Inhaled NO significantly decreased the central venous pressure (CVP), from 16.2 ± 2.2 to 14.6 ± 2.2mmHg (P < 0.0001), and the transpulmonary pressure gradient between the CVP and left atrial pressure, from 9.9 ± 2.9 to 8.4 ± 2.7mmHg (P < 0.0001). It also increased the systolic systemic arterial pressure from 71.9 ± 15.2 to 76.8 ± 14.5mmHg (P < 0.05). In 26 patients with additional fenestration, inhaled NO led to a significant improvement in SaO2 from 90.1% ± 9.6% to 93.3% ± 7.9% (P < 0.01). However, patients with a CVP <15mmHg or a transpulmonary pressure gradient <8mmHg, or both, after the Fontan-type operation, showed no significant changes in hemodynamics during inhaled NO therapy. Conclusions. We propose that a CVP ≥15mmHg or a transpulmonary pressure gradient ≥8mmHg, or both, after Fontan-type operations are appropriate indications for inhaled NO therapy.
AB - Purpose. Inhaled nitric oxide (NO) therapy is a newly developed strategy designed to reduce pulmonary vascular resistance after the Fontan-type operation. We reviewed our experience to evaluate its efficacy and true indications. Methods. We retrospectively examined 47 children who received inhaled NO therapy after the Fontan-type operation between August 1996 and December 2002. The maximal dose of NO ranged from 5 to 30ppm (median 10ppm), and the duration of inhaled NO therapy ranged from 5h to 52 days (median 2 days). Results. Inhaled NO significantly decreased the central venous pressure (CVP), from 16.2 ± 2.2 to 14.6 ± 2.2mmHg (P < 0.0001), and the transpulmonary pressure gradient between the CVP and left atrial pressure, from 9.9 ± 2.9 to 8.4 ± 2.7mmHg (P < 0.0001). It also increased the systolic systemic arterial pressure from 71.9 ± 15.2 to 76.8 ± 14.5mmHg (P < 0.05). In 26 patients with additional fenestration, inhaled NO led to a significant improvement in SaO2 from 90.1% ± 9.6% to 93.3% ± 7.9% (P < 0.01). However, patients with a CVP <15mmHg or a transpulmonary pressure gradient <8mmHg, or both, after the Fontan-type operation, showed no significant changes in hemodynamics during inhaled NO therapy. Conclusions. We propose that a CVP ≥15mmHg or a transpulmonary pressure gradient ≥8mmHg, or both, after Fontan-type operations are appropriate indications for inhaled NO therapy.
KW - Congenital heart disease
KW - Fontan-type operation
KW - Nitric oxide
UR - http://www.scopus.com/inward/record.url?scp=16644366521&partnerID=8YFLogxK
U2 - 10.1007/s00595-004-2887-1
DO - 10.1007/s00595-004-2887-1
M3 - 学術論文
C2 - 15622461
AN - SCOPUS:16644366521
SN - 0941-1291
VL - 35
SP - 31
EP - 35
JO - Surgery Today
JF - Surgery Today
IS - 1
ER -