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1
Height and weight gain after total correction of Fallot's tetralogy.法洛四联症完全矫正术后的身高和体重增长
Br Heart J. 1978 Apr;40(4):416-20. doi: 10.1136/hrt.40.4.416.
2
Long-term shunt palliation for Fallot's tetralogy.法洛四联症的长期分流姑息治疗。
Scand J Thorac Cardiovasc Surg. 1976;10(2):126-30. doi: 10.3109/14017437609167779.
3
[Growth in 60 children with surgically corrected tetralogy of Fallot].
An Esp Pediatr. 1982 Nov;17(5):371-8.
4
[Complete correction of Fallot's tetralogy with a Waterston shunt].
Arch Mal Coeur Vaiss. 1979 May;72(5):478-83.
5
[Acquired pulmonary atresia complicating tetralogy of Fallot].[后天性肺动脉闭锁合并法洛四联症]
Arch Mal Coeur Vaiss. 1979 May;72(5):484-9.
6
Classic shunting operations for congenital cyanotic heart defects.先天性青紫型心脏缺陷的经典分流手术。
J Thorac Cardiovasc Surg. 1982 Jul;84(1):88-96.
7
The modified Blalock-Taussig shunt: clinical impact and morbidity in Fallot's tetralogy in the current era.改良布莱洛克-陶西格分流术:当代法洛四联症中的临床影响及发病率
J Thorac Cardiovasc Surg. 1997 Jul;114(1):25-30. doi: 10.1016/S0022-5223(97)70113-2.
8
Abnormalities of conduction after total correction of Fallot's tetralogy: a prospective study.法洛四联症完全矫正术后的传导异常:一项前瞻性研究。
J Pak Med Assoc. 2002 Feb;52(2):77-82.
9
Palliative surgery in tetralogy of Fallot.法洛四联症的姑息性手术
Can J Surg. 1981 Sep;24(5):475-9.
10
Total correction of Fallot's tetralogy.
Scand J Thorac Cardiovasc Surg. 1976;10(2):131-4. doi: 10.3109/14017437609167780.

引用本文的文献

1
Identification of risk factors affecting catch-up growth after infant congenital heart disease surgery: rationale and design of a multicentre prospective cohort study in China.影响婴幼儿先天性心脏病术后追赶生长的风险因素识别:一项多中心前瞻性队列研究在中国的理论基础与设计。
BMJ Open. 2019 Aug 20;9(8):e030084. doi: 10.1136/bmjopen-2019-030084.
2
Linear growth in relation to the circulating concentration of insulin-like growth factor-I in young children with acyanotic congenital heart disease with left to right shunts before versus after surgical intervention.患有左向右分流的非青紫型先天性心脏病幼儿在手术干预前后,线性生长与胰岛素样生长因子-I循环浓度的关系。
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3
Long term somatic growth after repair of tetralogy of Fallot: evidence for restoration of genetic growth potential.法洛四联症修复术后的长期躯体生长:遗传生长潜力恢复的证据
Heart. 2003 Nov;89(11):1340-3. doi: 10.1136/heart.89.11.1340.

本文引用的文献

1
The effect of surgery on the growth of patients with patent ductus arteriosus.
J Pediatr. 1951 Sep;39(3):330-6. doi: 10.1016/s0022-3476(51)80155-0.
2
[Physical and mental development in children with congenital heart and vascular abnormalities].[先天性心血管异常患儿的身心发育]
Arch Kinderheilkd Suppl. 1962;47:1-61.
3
Growth disturbance in congenital heart disease.先天性心脏病中的生长发育障碍。
J Pediatr. 1962 Sep;61:418-29. doi: 10.1016/s0022-3476(62)80373-4.
4
ORGAN AND CELLULAR DEVELOPMENT IN CONGENITAL HEART DISEASE AND IN ALIMENTARY MALNUTRITION.先天性心脏病与营养性营养不良中的器官和细胞发育
J Pediatr. 1965 Sep;67:447-58. doi: 10.1016/s0022-3476(65)80406-1.
5
[Treatment of Fallot's tetralogy in children under 1 year of age].[1岁以下儿童法洛四联症的治疗]
Rozhl Chir. 1962 Mar;41:181-3.
6
Growth failure associated with congenital heart disease.与先天性心脏病相关的生长发育迟缓。
Clin Proc Child Hosp Dist Columbia. 1959 Apr;15(4):87-92.
7
Anatomic features of growth failure in congenital heart disease.先天性心脏病生长发育迟缓的解剖学特征。
Pediatrics. 1967 Mar;39(3):433-40.
8
Standards from birth to maturity for height, weight, height velocity, and weight velocity: British children, 1965. II.1965年英国儿童从出生到成年的身高、体重、身高增长速度和体重增长速度标准:第二部分。
Arch Dis Child. 1966 Dec;41(220):613-35. doi: 10.1136/adc.41.220.613.
9
Growth history of children with congenital heart defects. I. Effect of operative intervention.先天性心脏病患儿的生长史。I. 手术干预的影响。
Child Dev. 1969 Mar;40(1):315-46.
10
Total correction of tetralogy of Fallot in infancy.婴儿期法洛四联症的根治术
J Thorac Cardiovasc Surg. 1973 Jan;65(1):45-57.

法洛四联症完全矫正术后的身高和体重增长

Height and weight gain after total correction of Fallot's tetralogy.

作者信息

Page R E, Deverall P B, Watson D A, Scott O

出版信息

Br Heart J. 1978 Apr;40(4):416-20. doi: 10.1136/hrt.40.4.416.

DOI:10.1136/hrt.40.4.416
PMID:646909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC482813/
Abstract

In a consecutive series of 100 cases of Fallot's tetralogy undergoing total correction, the mean birthweight was found to be just below the 50th centile. Blalock-Taussig or Waterston shunts were performed in 45 patients. Before their shunt operations a significant number of patients had become retarded in height and weight development but after the shunt operations many patients showed accelerated height and weight gain. Of the 73 patients followed up 2 years after correction, 23 had experienced accelerated development in both weight and height, but 11 patients remained on or below the 3rd centile for weight and height. In terms of the age at shunting, the oxygen saturation immediately before total correction, the age at total correction, the number of ventriculotomy patch repairs, and the post-correction ventricular pressure ratios, no significant difference could be detected between those 23 patients who had undergone accelerated development and those 11 who had remained retarded. More shunts, particularly of the Waterston type, were performed in the retarded group.

摘要

在连续100例接受根治手术的法洛四联症患者中,平均出生体重略低于第50百分位数。45例患者进行了锁骨下动脉-肺动脉吻合术(Blalock-Taussig分流术)或升主动脉-肺动脉吻合术(Waterston分流术)。在进行分流手术前,相当多的患者身高和体重发育迟缓,但分流手术后,许多患者身高和体重增加加速。在73例根治术后随访2年的患者中,23例体重和身高均加速发育,但11例患者体重和身高仍处于或低于第3百分位数。就分流时的年龄、根治术前即刻的血氧饱和度、根治时的年龄、心室切开补片修复的次数以及根治术后心室压力比值而言,在23例加速发育的患者与11例发育迟缓的患者之间未检测到显著差异。发育迟缓组进行了更多的分流手术,尤其是Waterston分流术。