Anesthetic implications of ornithine transcarbamylase deficiency

被引:13
作者
Dutoit, Andrea P. [1 ]
Flick, Randall R. [1 ]
Sprung, Juraj [1 ]
Babovic-Vuksanovic, Dusica [2 ]
Weingarten, Toby N. [1 ]
机构
[1] Mayo Clin, Coll Med, Dept Anesthesiol, Rochester, MN USA
[2] Mayo Clin, Coll Med, Dept Med Genet, Rochester, MN USA
关键词
ornithine transcarbamylase deficiency; pediatric anesthesia; general anesthesia; UREA-CYCLE DISORDERS; LIVER-TRANSPLANTATION; MANAGEMENT; ENCEPHALOPATHY; MULTICENTER; SURGERY;
D O I
10.1111/j.1460-9592.2010.03322.x
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
P>Background: Ornithine transcarbamylase deficiency (OTCD) is an X-linked urea cycle disorder associated with potentially fatal episodes of hyperammonemia. Children with OTCD often require anesthesia. There is insufficient information regarding perioperative complications and optimal management of anesthesia in these patients. Aim: To retrospectively review the medical records of children with OTCD to ascertain the nature and frequency of peri-procedural complications. Methods/Materials: The electronic medical records of Mayo Clinic patients with OTCD who underwent anesthesia between the dates of January 2003 and September 2009 were reviewed. Results: Nine patients with OTCD underwent 25 anesthetics using a variety of anesthetic techniques, including four major surgeries. Eleven procedures were performed prior to OTCD diagnosis and those patients were not receiving therapy for a urea cycle disorder. In the other cases, patients were on a variety of therapies for OTCD. Fourteen patients were outpatient procedures. Clinical signs of postoperative metabolic decompensation did not occur. Conclusions: In this series, patients with OTCD tolerated anesthesia well. Choice of perioperative management of OTCD and the choice of anesthetic technique should be individualized and based on clinical circumstances, but should have the underlying aim of minimizing protein catabolism. It appears patients with stable OTCD may undergo minor procedures as outpatients safely.
引用
收藏
页码:666 / 673
页数:8
相关论文
共 16 条
[1]   Long-term management of patients with urea cycle disorders [J].
Berry, GT ;
Steiner, RD .
JOURNAL OF PEDIATRICS, 2001, 138 (01) :S56-S60
[2]  
Berry GT, 2001, J PEDIAT S, V138, pS60
[3]  
BRUSILOW SW, 1979, LANCET, V1, P124
[4]   Hypocitrullinemia in expanded newborn screening by LC-MS/MS is not a reliable marker for ornithine transcarbamylase deficiency [J].
Cavicchi, C. ;
Malvagia, S. ;
Ia Marca, G. ;
Gasperini, S. ;
Donati, M. A. ;
Zammarchi, E. ;
Guerrini, R. ;
Morrone, A. ;
Pasquini, E. .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2009, 49 (05) :1292-1295
[5]   Fatal late-onset ornithine transcarbamylase deficiency after coronary artery bypass surgery [J].
Chiong, Mary Anne ;
Bennetts, Bruce H. ;
Strasser, Simone I. ;
Wilcken, Bridget .
MEDICAL JOURNAL OF AUSTRALIA, 2007, 186 (08) :418-419
[6]   Survival after treatment with phenylacetate and benzoate for urea-cycle disorders [J].
Enns, Gregory M. ;
Berry, Susan A. ;
Berry, Gerard T. ;
Rhead, William J. ;
Brusilow, Saul W. ;
Hamosh, Ada .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (22) :2282-2292
[7]   Management and outcome of neonatal-onset ornithine transcarbamylase deficiency following liver transplantation at 60 days of life [J].
Ensenauer, R ;
Tuchman, M ;
El-Youssef, M ;
Kotagal, S ;
Ishitani, MB ;
Matern, D ;
Babovic-Vuksanovic, D .
MOLECULAR GENETICS AND METABOLISM, 2005, 84 (04) :363-366
[8]   ORTHOTOPIC LIVER-TRANSPLANTATION FOR ORNITHINE TRANSCARBAMYLASE DEFICIENCY WITH HYPERAMMONEMIC ENCEPHALOPATHY [J].
HASEGAWA, T ;
TZAKIS, AG ;
TODO, S ;
REYES, J ;
NOUR, B ;
FINEGOLD, DN ;
STARZL, TE .
JOURNAL OF PEDIATRIC SURGERY, 1995, 30 (06) :863-865
[9]   Ornithine transcarbamylase deficiency presenting as encephalopathy during adulthood following bariatric surgery [J].
Hu, William T. ;
Kantarci, Orhun H. ;
Merritt, J. Lawrence, II ;
McGrann, Pamela ;
Dyck, P. James B. ;
Lucchinetti, Claudia F. ;
Tippmann-Peikert, Maja .
ARCHIVES OF NEUROLOGY, 2007, 64 (01) :126-128
[10]   Current role of liver transplantation for the treatment of urea cycle disorders: A review of the worldwide English literature and 13 cases at Kyoto University [J].
Morioka, D ;
Kasahara, M ;
Takada, Y ;
Shirouzu, Y ;
Taira, K ;
Sakamoto, S ;
Uryuhara, K ;
Egawa, H ;
Shimada, H ;
Tanaka, A .
LIVER TRANSPLANTATION, 2005, 11 (11) :1332-1342