Abstract:Background. While single-institution studies reported the indications and outcomes of tracheostomy in children with congenital heart disease (CHD), no national analyses have been performed. We sought to examine the indications, performance, outcomes, and resource utilization of tracheostomy in children with CHD using a nationally representative database.Methods. We identified all children undergoing tracheostomy in the Kids’ Inpatient Database 1997 through 2009, and we compared children with CHD to children wi… Show more
“…21 In this study, the rate was 0.4% among infants with CHD. Compared with our study, previous reports tended to focus on broader pediatric populations or were hospital-based, single-institution investigations with limited numbers of participants.…”
Section: Discussionmentioning
confidence: 81%
“…The reported incidence of tracheostomy in children with CHD is low in the literature, 17,18,21 with a rate of 0.2% among pediatric subjects undergoing cardiovascular surgery 17 and 3.5% among pediatric admissions with CHD. 21 In this study, the rate was 0.4% among infants with CHD.…”
Section: Discussionmentioning
confidence: 84%
“…6,[8][9][10][11][12] However, most studies have focused on the indications for tracheostomy, the subsequent outcomes, or resource utilization. 6,[10][11][12][13][14][15][16][17][18][19][20][21][22] Data are scant regarding the epidemiological risk factors for tracheostomy in CHD, and there have been no large-scale population-based studies. Furthermore, among infants with CHD requiring a tracheostomy, previous studies have failed to investigate either the overall mortality risk or the mortality risk stratified by a follow-up period.…”
“…21 In this study, the rate was 0.4% among infants with CHD. Compared with our study, previous reports tended to focus on broader pediatric populations or were hospital-based, single-institution investigations with limited numbers of participants.…”
Section: Discussionmentioning
confidence: 81%
“…The reported incidence of tracheostomy in children with CHD is low in the literature, 17,18,21 with a rate of 0.2% among pediatric subjects undergoing cardiovascular surgery 17 and 3.5% among pediatric admissions with CHD. 21 In this study, the rate was 0.4% among infants with CHD.…”
Section: Discussionmentioning
confidence: 84%
“…6,[8][9][10][11][12] However, most studies have focused on the indications for tracheostomy, the subsequent outcomes, or resource utilization. 6,[10][11][12][13][14][15][16][17][18][19][20][21][22] Data are scant regarding the epidemiological risk factors for tracheostomy in CHD, and there have been no large-scale population-based studies. Furthermore, among infants with CHD requiring a tracheostomy, previous studies have failed to investigate either the overall mortality risk or the mortality risk stratified by a follow-up period.…”
“…Tartrazine toxicity is said to result from the invivo metabolism of its azo bonds which occurs in the liver and the intestine, thereby leading to production of toxic oxidative metabolites such as aryl amines, reactive amines, and free radicals [8,9]. Also, tartrazine dye have been found to covalently react with and destroy the protein active site and configuration of enzymes resulting in loss of normal functioning to the enzyme which may lead to several metabolic consequences [8,9]. Excess in-take of tartrazine dye has been reported to cause attention deficit disorders, allergic and intolerance reactions such as itching, migraines, sleep disturbance, anxiety, blurred vision, and general weakness in children [7,9].…”
Aim: To assess the effect of tartrazine at ADI doses on ovarian integrity (the weight and histology of the ovary), reproductive fertility hormones (luteinizing hormones (LH), follicle stimulating hormone (FSH) and prolactin (PRL)) and oxidative stress markers (glutathione peroxidase (GPX) and superoxide dismutase (SOD)) over a period of 30 and 60 days in albino rats.
Study Design: A total of 63 female rats weighing approximately 0.2kg were divided into two phases. In phase 1 (30 days treatment period), the rats were divided into 2 groups - designated tartrazine treated group (TTG1) consisting of 20 rats and control untreated group (CUG1) consisting of 15 rats. In phase 2 (60 days treatment period), the rats were again divided into 2 groups – tartrazine treated group (TTG2) consisting of 16 rats and control untreated group (CUG2) consisting of 12 rats. The acceptable daily intake (ADI) of 7.5mg/kg of the dye was administered orally while the control groups were given food and water only.
Methodology: At the end of the study, the animals were anaesthetized and 5 mL of whole blood samples was collected by means of cardiac puncture into plain bottles, later spun at 4000 rpm for 5 minutes to obtain serum. The laboratory analysis of LH, FSH and PRL as well as GPX and SOD activity were based on Enzyme Linked Immunosorbent Assay (ELISA) Technique using rat-specific kits. Ovarian tissues collected were weighed using electronic balance, washed in normal saline, fixed in 10% formalin saline, embedded in paraffin wax, 5μm thick sections were obtained by rotary microtome, stained using Haematoxylin & Eosin and examined using digital Olympus microscopic.
Results: Non-significant higher values in the absolute weight of the ovary (WOV), FSH, LH, and PRL while non-significant lower values in GPX and SOD were observed in the treated rats against control rats over a period of 30 and 60 days at P=.05. The histological examination over a period of 30 days did not indicate any alteration but hydropic dilation and structural alterations were seen after 60 days.
Conclusion: The administration of ADI doses of tartrazine over a period of 60 days affected the integrity of the ovary mildly as observed in the histology but did not markly reflect on the biochemical markers in the plasma as well as the weight of the ovary.
“…Specifically, you wonder whether recommending a tracheostomy soon, or after another few weeks of recovery, would benefit the child. The question is being asked with increasing frequency at children's bedsides in both general and cardiac ICUs (2).…”
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