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1.
J Genet Couns ; 26(4): 852-858, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28181058

RESUMO

Reimbursement for genetic counseling services was examined at a single institution. Patient encounters utilizing the 96040 CPT® code from 7/31/2009 through 7/31/2013 were reviewed. Exclusion criteria included billing records of patients seen by a physician the same day, self-pay, Medicaid, and Medicare patients. Of the 8,630 encounters with a genetic counselor, 582 encounters were eligible for review. Descriptive statistics (i.e., percentage of encounters receiving some level of reimbursement, average reimbursement rate, number of third party payors providing any level of reimbursement, and number of ICD-9 codes receiving any level of reimbursement) depicted reimbursement of the 96040 CPT® code for the encounters analyzed. Statistical analysis found a significant difference in reimbursement between third party payors that do and do not credential genetic counselors (p < .0001). There was no statistically significant difference between reimbursement rates for primary diagnostic ICD-9 codes when compared to primary diagnostic ICD-9 V codes used. Results will provide a useful baseline for local and national comparisons due to the paucity of data regarding CPT® 96040.


Assuntos
Aconselhamento Genético/economia , Reembolso de Seguro de Saúde/economia , Classificação Internacional de Doenças/economia , Humanos , Estados Unidos
2.
S D Med ; Spec No: 12-5, 17, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21717811

RESUMO

Obesity risk is amplified in the presence of obese relatives yet does not usually follow classic Mendelian inheritance patterns. A combination of gene mutations, deletions and single nucleotide polymorphisms are all known to contribute to obesity. Most cases are polygenic, the result of multiple genes interacting with a changing environment. Each "obesity gene" only makes a small contribution to phenotype, but collectively, inherited genetic variations play a major role in determining body mass and how the body responds to physical activity and nutrition. While obesity is most commonly associated with polygenic inheritance, there are other instances in which the cause is monogenic or syndromic. Monogenic obesity typically is caused by a single gene mutation with severe obesity as the main symptom. Syndromic obesity, on the other hand, has many characteristics, of which obesity is one symptom.


Assuntos
Obesidade/genética , Síndrome de Bardet-Biedl/genética , Aberrações Cromossômicas , Humanos , Polimorfismo de Nucleotídeo Único/fisiologia , Síndrome de Prader-Willi/genética , Aumento de Peso/genética
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