Safety of inhaled nitric oxide after lung transplantation

被引:23
作者
Cornfield, DN
Milla, CE
Haddad, IY
Barbato, JE
Park, SJ
机构
[1] Univ Minnesota, Sch Med, Div Pediat Pulmonol & Crit Care Med, Dept Pediat, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Dept Surg, Minneapolis, MN 55455 USA
[3] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA
[4] Div Cardiovasc & Thorac Surg, Dept Pediat, Minneapolis, MN USA
[5] Div Cardiovasc & Thorac Surg, Dept Surg, Minneapolis, MN USA
关键词
D O I
10.1016/S1053-2498(02)00809-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The present study tests the hypothesis that therapy with inhaled nitric oxide (iNO) at the time of lung transplantation in patients undergoing bilateral single lung transplantation: (i) is safe; and (ii) does not increase either the duration of mechanical ventilation or the incidence of acute graft dysfunction. Methods: We conducted a prospective, non-randomized trial of iNO at 20 parts per million. The treatment group was comprised of 14 patients (10 females, 4 males) undergoing lung transplantation to address severe end-stage lung disease and pulmonary hypertension (mean pulmonary artery pressure > 30 mmHg). Clinical and histologic parameters were compared with 22 historical control subjects who were matched with the study population for age, diagnosis and disease severity (17 females, 5 males) and had undergone lung transplantation in the preceding 2-year time period. No significant differences were noted between the 2 study groups at baseline. Results: No toxic effect of iNO treatment was evident. Although the incidence of acute graft dysfunction was the same in both groups, the occurrence of acute graft rejection in the initial 4 weeks after transplant was less frequent in the iNO group than in the control group (7% vs 32%, p = 0.05). Fifty percent of the treatment group, as compared with 22% of the control group, were discharged from the hospital within 2 weeks of the procedure (p = 0.05). Conclusions: Early initiation of iNO in lung transplant patients with pulmonary hypertension is safe and may decrease the incidence of acute graft rejection. We speculate that iNO may exert an immunomodulatory effect.
引用
收藏
页码:903 / 907
页数:5
相关论文
共 13 条
[1]   INHALED NITRIC-OXIDE IN THE TREATMENT OF POSTOPERATIVE GRAFT DYSFUNCTION AFTER LUNG TRANSPLANTATION [J].
ADATIA, I ;
LILLIHEI, C ;
ARNOLD, JH ;
THOMPSON, JE ;
PALAZZO, R ;
FACKLER, JC ;
WESSEL, DL .
ANNALS OF THORACIC SURGERY, 1994, 57 (05) :1311-1318
[2]  
ALBINA JE, 1991, J IMMUNOL, V147, P144
[3]   Medical progress - Lung transplantation [J].
Arcasoy, SM ;
Kotloff, RM .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (14) :1081-1091
[4]   Prevention of ischemia-reperfusion lung injury by inhaled nitric oxide in neonatal piglets [J].
BarbotinLarrieu, F ;
Mazmanian, M ;
Baudet, B ;
Detruit, H ;
Chapelier, A ;
Libert, JM ;
Dartevelle, P ;
Herve, P .
JOURNAL OF APPLIED PHYSIOLOGY, 1996, 80 (03) :782-788
[5]  
De C.R., 1995, J CLIN INVEST, V96, P60
[6]   Inhaled nitric oxide at the time of harvest improves early lung allograft function [J].
Fujino, S ;
Nagahiro, I ;
Triantafillou, AN ;
Boasquevisque, CHR ;
Yano, M ;
Cooper, JD ;
Patterson, GA .
ANNALS OF THORACIC SURGERY, 1997, 63 (05) :1383-1389
[7]  
Fujino S, 1997, J HEART LUNG TRANSPL, V16, P1073
[8]   EVIDENCE THAT NITRIC-OXIDE PRODUCTION BY INVIVO ALLOSENSITIZED CELLS INHIBITS THE DEVELOPMENT OF ALLOSPECIFIC CTL [J].
LANGREHR, JM ;
DULL, KE ;
OCHOA, JB ;
BILLIAR, TR ;
ILDSTAD, ST ;
SCHRAUT, WH ;
SIMMONS, RL ;
HOFFMAN, RA .
TRANSPLANTATION, 1992, 53 (03) :632-640
[9]   Newly developed solution enhances thirty-hour preservation in a canine lung transplantation model [J].
Liu, CJ ;
Ueda, M ;
Kosaka, S ;
Hirata, T ;
Yokomise, H ;
Inui, K ;
Hitomi, S ;
Wada, H .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1996, 112 (03) :569-576
[10]   INHALED NITRIC-OXIDE AS A CAUSE OF SELECTIVE PULMONARY VASODILATATION IN PULMONARY-HYPERTENSION [J].
PEPKEZABA, J ;
HIGENBOTTAM, TW ;
DINHXUAN, AT ;
STONE, D ;
WALLWORK, J .
LANCET, 1991, 338 (8776) :1173-1174