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US physician practices for diagnosing familial hypercholesterolemia: data from the CASCADE-FH registry.
Ahmad, Zahid S; Andersen, Rolf L; Andersen, Lars H; O'Brien, Emily C; Kindt, Iris; Shrader, Peter; Vasandani, Chandna; Newman, Connie B; deGoma, Emil M; Baum, Seth J; Hemphill, Linda C; Hudgins, Lisa C; Ahmed, Catherine D; Kullo, Iftikhar J; Gidding, Samuel S; Duffy, Danielle; Neal, William; Wilemon, Katherine; Roe, Matthew T; Rader, Daniel J; Ballantyne, Christie M; Linton, MacRae F; Duell, P Barton; Shapiro, Michael D; Moriarty, Patrick M; Knowles, Joshua W.
Afiliação
  • Ahmad ZS; Division of Nutrition and Metabolic Diseases, Department of Internal Medicine, University of Texas Southwestern, Dallas, TX, USA.
  • Andersen RL; Lancaster General Health/Penn Medicine, Lancaster, PA, USA.
  • Andersen LH; Lancaster General Health/Penn Medicine, Lancaster, PA, USA.
  • O'Brien EC; Department of Medicine, Duke Clinical Research Institute, Durham, NC, USA.
  • Kindt I; The FH Foundation, South Pasadena, CA, USA.
  • Shrader P; Department of Medicine, Duke Clinical Research Institute, Durham, NC, USA.
  • Vasandani C; Division of Nutrition and Metabolic Diseases, Department of Internal Medicine, University of Texas Southwestern, Dallas, TX, USA.
  • Newman CB; Department of Medicine, New York University School of Medicine, New York, NY, USA.
  • deGoma EM; Department of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Baum SJ; Preventive Cardiology Inc., Boca Raton, FL, USA.
  • Hemphill LC; Cardiology Division, Massachusetts General Hospital, Boston, MA, USA.
  • Hudgins LC; The Rogosin Institute, New York, NY, USA.
  • Ahmed CD; The FH Foundation, South Pasadena, CA, USA.
  • Kullo IJ; Mayo Clinic, Rochester, MN, USA.
  • Gidding SS; Department of Pediatrics, Nemours Cardiac Center, Wilmington, DE, USA.
  • Duffy D; Division of Cardiology, Thomas Jefferson University, Philadelphia, PA, USA.
  • Neal W; Department of Pediatrics, West Virginia University, Morgantown, WV, USA.
  • Wilemon K; The FH Foundation, South Pasadena, CA, USA.
  • Roe MT; Department of Medicine, Duke Clinical Research Institute, Durham, NC, USA.
  • Rader DJ; Department of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Ballantyne CM; Department of Medicine, Baylor College of Medicine, Houston, TX, USA.
  • Linton MF; Vanderbilt University School of Medicine, Nashville, TN, USA.
  • Duell PB; Knight Cardiovascular Institute, Oregon Health and Science University, Portland, OR, USA.
  • Shapiro MD; Knight Cardiovascular Institute, Oregon Health and Science University, Portland, OR, USA.
  • Moriarty PM; University of Kansas Medical Center, Kansas City, KS, USA.
  • Knowles JW; Department of Medicine, Stanford University, Stanford, CA, USA. Electronic address: knowlej@stanford.edu.
J Clin Lipidol ; 10(5): 1223-9, 2016.
Article em En | MEDLINE | ID: mdl-27678440
ABSTRACT

BACKGROUND:

In the US familial hypercholesterolemia (FH), patients are underidentified, despite an estimated prevalence of 1200 to 1500. Criteria to identify FH patients include Simon Broome, Dutch Lipid Clinic Network (DLCN), or Make Early Diagnosis to Prevent Early Deaths (MEDPED). The use of these criteria in US clinical practices remains unclear.

OBJECTIVE:

To characterize the FH diagnostic criteria applied by US lipid specialists participating in the FH Foundation's CASCADE FH (CAscade SCreening for Awareness and DEtection of Familial Hypercholesterolemia) patient registry.

METHODS:

We performed an observational, cross-sectional analysis of diagnostic criteria chosen for each adult patient, both overall and by baseline patient characteristics, at 15 clinical sites that had contributed data to the registry as of September 8, 2015. A sample of 1867 FH adults was analyzed. The median age at FH diagnosis was 50 years, and the median pretreatment low-density lipoprotein cholesterol (LDL-C) value was 238 mg/dL. The main outcome was the diagnostic criteria chosen. Diagnostic criteria were divided into five nonexclusive categories "clinical diagnosis," MEDPED, Simon Broome, DLCN, and other.

RESULTS:

Most adults enrolled in CASCADE FH (55.0%) received a "clinical diagnosis." The most commonly used formal criteria was Simon-Broome only (21%), followed by multiple diagnostic criteria (16%), MEDPED only (7%), DLCN only (1%), and other (0.5%), P < .0001. Of the patients with only a "clinical diagnosis," 93% would have met criteria for Simon Broome, DLCN, or MEDPED based on the data available in the registry.

CONCLUSIONS:

Our findings demonstrate heterogeneity in the application of FH diagnostic criteria in the United States. A nationwide consensus definition may lead to better identification, earlier treatment, and ultimately CHD prevention.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperlipoproteinemia Tipo II Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperlipoproteinemia Tipo II Idioma: En Ano de publicação: 2016 Tipo de documento: Article