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10.3171/2015.10.PEDS15369

http://scihub22266oqcxt.onion/10.3171/2015.10.PEDS15369
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C4876706!4876706!26799408
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suck abstract from ncbi


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pmid26799408      J+Neurosurg+Pediatr 2016 ; 17 (5): 525-32
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  • Chiari malformation Type I surgery in pediatric patients Part 2: complications and the influence of comorbid disease in California, Florida, and New York #MMPMID26799408
  • Greenberg JK; Olsen MA; Yarbrough CK; Ladner TR; Shannon CN; Piccirillo JF; Anderson RCE; Wellons JC; Smyth MD; Park TS; Limbrick DD
  • J Neurosurg Pediatr 2016[May]; 17 (5): 525-32 PMID26799408show ga
  • Objective: Chiari malformation Type I (CM-I) is a common and often debilitating pediatric neurological disease. However, efforts to guide preoperative counseling and improve outcomes research are impeded by reliance on small, singlecenter studies. Consequently, the objective of this study was to investigate CM-I surgical outcomes using population-level administrative billing data. Methods: The authors used Healthcare Cost and Utilization Project State Inpatient Databases (SID) to study pediatric patients undergoing surgical decompression for CM-I from 2004 to 2010 in California, Florida, and New York. They assessed the prevalence and influence of preoperative complex chronic conditions (CCC) among included patients. Outcomes included medical and surgical complications within 90 days of treatment. Multivariate logistic regression was used to identify risk factors for surgical complications. Results: A total of 936 pediatric CM-I surgeries were identified for the study period. Overall, 29.2% of patients were diagnosed with syringomyelia and 13.7% were diagnosed with scoliosis. Aside from syringomyelia and scoliosis, 30.3% of patients had at least 1 CCC, most commonly neuromuscular (15.2%) or congenital or genetic (8.4%) disease. Medical complications were uncommon, occurring in 2.6% of patients. By comparison, surgical complications were diagnosed in 12.7% of patients and typically included shunt-related complications (4.0%), meningitis (3.7%), and other neurosurgery-specific complications (7.4%). Major complications (e.g., stroke or myocardial infarction) occurred in 1.4% of patients. Among children with CCCs, only comorbid hydrocephalus was associated with a significantly increased risk of surgical complications (OR 4.5, 95% CI 2.5?8.1). Conclusions: Approximately 1 in 8 pediatric CM-I patients experienced a surgical complication, whereas medical complications were rare. Although CCCs were common in pediatric CM-I patients, only hydrocephalus was independently associated with increased risk of surgical events. These results may inform patient counseling and guide future research efforts.
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