Severe motor and intellectual disability

  • 文章类型: Journal Article
    Nutritional metabolism is complex in pediatric patients with severe motor and intellectual disability (SMID), and therefore, appropriate estimation of the energy requirements is difficult. Focusing on ghrelin\'s role in energy metabolism regulation, we investigated plasma ghrelin levels in pediatric SMID patients and analyzed its nutritional significance as a regulatory marker of energy reserve.
    Fasting plasma total, acyl, and des-acyl ghrelin levels in 40 patients with SMID, including cerebral palsy (CP) (n = 20) and muscular disease (MD) (n = 8), and healthy controls (n = 13) were investigated. The correlations of plasma ghrelin levels with anthropometry, blood nutritional markers, energy intake, and resting energy expenditure (REE) measured with indirect calorimetry were analyzed. A p value < 0.05 was considered significant.
    SMID patients had significantly higher acyl ghrelin, and lower body mass index (BMI), z-scores of body weight (BW), body height and BMI, and albumin than controls. CP patients had significantly higher total and acyl ghrelin, z-score of the mid-upper arm circumference (MUAC), retinol-binding protein, transthyretin, creatinine, and glucose than MD patients. Total and acyl ghrelin in CP patients and des-acyl ghrelin in MD patients had significant negative correlations with MUAC and upper arm fat area. In CP patients, total and acyl ghrelin had significant positive correlations with REE/BW (kcal/kg), and total ghrelin was predictive of REE/BW (r2 = 0.625, p < 0.0001).
    An increase in acyl ghrelin observed in SMID patients possibly indicates energy reserve deficiency. In CP patients, total and acyl ghrelin inversely reflected total body fat mass, resulting in strongly positive correlations with REE/BW. The measurement of plasma ghrelin may be useful to assess nutritional metabolism and energy reserve in pediatric SMID patients, such as CP and MD patients.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    目的:气管切开或气管食管改道(TED)后,气管无名动脉瘘(TIF)是一种罕见但危及生命的并发症。尽管已经报道了成功的TIF手术干预,在重度运动和智力残疾(SMID)患者中进行的研究很少.因此,我们旨在分析SMID患者的TIF,以阐明预测TIF发生的临床变量以及为挽救TIF的生命而采取的适当管理.
    方法:我们回顾性回顾了2006年至2012年间接受外科气管切开术和TED的SMID患者的记录,并确定了TIF患者。当TIF发生时,我们获得了临床状态和急诊处理。
    结果:在研究期间接受气管切开术或TED的70名患者中,三名患者患有TIF;在一个病例中,在TED之前通过结扎无名动脉来避免TIF。TIF在接受气管切开术和TED的患者中的发生率为2.3%和7.4%,分别。气管造口术和TIF之间的间隔为14-50个月。
    结论:SMID患者发生TIF的风险增加。及时诊断和手术干预以控制出血是目前唯一有效的治疗方法。
    OBJECTIVE: Tracheo-innominate artery fistula (TIF) is a rare but life-threatening complication following tracheostomy or tracheoesophageal diversion (TED). Although successful surgical intervention for TIF has been reported, few studies have been performed in patients with severe motor and intellectual disability (SMID). Therefore, we aimed to analyze TIF in patients with SMID to clarify the clinical variables predicting the occurrence and adequate management for lifesaving of TIF.
    METHODS: We retrospectively reviewed the records of patients with SMID undergoing surgical tracheostomy and TED between 2006 and 2012 and identified those with TIF. When TIF occurred, we obtained the clinical status and emergency management.
    RESULTS: Of 70 patients who underwent tracheostomy or TED during the study period, three patients had TIFs; in one case, TIF was avoided by ligation of the innominate artery before TED. The incidence of TIF in those undergoing tracheostomy and TED was 2.3% and 7.4%, respectively. The interval between tracheostomy and TIF was 14-50 months.
    CONCLUSIONS: Patients with SMID may have an increased risk of TIF. Prompt diagnosis and surgical intervention to control the bleeding is the only effective management at present.
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