Health Care Provider Resources | Genetic Conditions

Health Care Provider Resources | Genetic Conditions

Health Care Provider Resources 

More Information Newborn blood spot screening Newborn hearing screening Contact Us Oregon Genetics Program Staff

Time Out for Genetics Webinar Series

The Genetics in Primary Care Institute has created a webinar series for primary care clinicians, pediatricians, pediatric sub-specialists, family physicians, nurse practitioners, genetic counselors, geneticists, and other stakeholders.
These Time Out for Genetics webinars last a half hour, occur once a month, and are recorded so that you can also watch at your convenience. The webinars:

• provide stakeholders with information for better understanding of the relevance of genetic medicine to primary care
• increase awareness and education regarding the provision of genetic medicine in primary care
• improve health care providers’ understanding of their roles and the roles of others related to the provision of genetic medicine in primary care settings

You can register for upcoming webinars or listen to previously recorded webinars on the Genetics in Primary Care Institute webpage: http://www.medicalhomeinfo.org/GPCI.aspx

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Genetic Services in Oregon

• Oregon Genetics Clinic Contact List
• Indications for Referral: Preconception/Prenatal
• Indications for Referral: Pediatric
• Indications for Referral: Adult
• Northwest Regional Newborn Screening Program
  Screens newborns for endocrine, hemoglobin and metabolic disorders -- identifying infants who need immediate treatment to prevent developmental problems, mental retardation, or death. Identified infants are tracked to ensure they receive appropriate medical care.

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Genetics Privacy

• Oregon Genetics Privacy Opt-Out Factsheet
• Oregon Genetics Privacy Opt-Out Factsheet (Spanish version)
  Hoja Informativa Para Usuarios de Atención Médica, Privacidad Genética e Investigación 

• Oregon Genetics Privacy Opt-Out Sample notice (English version)
• Oregon Genetics Privacy Opt-Out Sample notice (Spanish version)
  EJEMPLO de Notificación, Declaración y Formulario de Opción de Exclusión 

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Genetics and Genomics for Health Professionals
This website provides reliable, up-to-date genetics and genomics information related to patient management, curricular resources, new National Institutes of Health and NHGRI research activities, and ethical, legal and social issues.

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Educational Materials

Information about Genetic Conditions

• GeneReviews
  Database of detailed reviews on genetic diseases created through funding from the National Library of Medicine, NIH and National Human Genome Research Institute, NIH.
• Online Mendelian Inheritance in Man (OMIM)
  Database and catalog of human genes and genetic disorders.

Pharmacogenomics

• Pharmacogenomics
  Contains news, background information, and education programs for pharmacists, including continuing education credits.  Materials were created by the School of Pharmacy at University of California, San Diego.

Practice Guidelines

• Evaluation of Genomic Applications in Practice and Prevention (EGAPP)
  EGAPPS's goal is to establish and evaluate a systematic, evidence-based process for assessing genetic tests and other applications of genomic techonology in transition from research to clinical and public health practice.

Recommendations:

• Testing for Cytochrome P450 Polymorphisms (CYP450) in Adults with Non-Psychotic Depression Prior to Treatment with Selective Serotonin Reuptake Inhibitors (SSRIs). (PDF 225KB)
• Can UGT1A1 Genotyping Reduce Morbidity and Mortality in Patients with Metastatic Colorectal Cancer Treated with Irinotecan? (PDF 201KB)
• Can tumor gene expression profiling improve outcomes in patients with breast cancer? (PDF 455KB)
• Genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives. (PDF 220KB)

Evidence Reports:

• Outcomes of Genetic Testing in Adults with a History of Venous Thromboembolism
  The Johns Hopkins University Evidence Based Practice Center - June 2009
• Can UGT1A1 Genotyping Reduce Morbidity and Mortality in Patients with Metastatic Colorectal Cancer Treated with Irinotecan? (PDF 502KB)
  CDC, in conjunction with IPMMS and RTI | January 2009
• EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome. (PDF 664KB)
  CDC/OPHG in collaboration with IPMMS | January 2009
• Impact of Gene Expression Profiling Tests on Breast Cancer Outcomes
  The Johns Hopkins University Evidence Based Practice Center | January 2008
• Hereditary Nonpolyposis Colorectal Cancer: Diagnostic Strategies and Their Implications
  Tufts New England Medical Center Evidence Based Practice Center | May 2007
• Testing for Cytochrome P450 Polymorphisms (CYP450) in Adults with Non-Psychotic Depression Prior to Treatment with Selective Serotonin Reuptake Inhibitors (SSRIs)
  Duke University AHRQ Evidence-based Practice Center | January 2007
• Genomic Tests for Ovarian Cancer Detection and Management
  Duke University AHRQ Evidence-based Practice Center | October 2006

• U.S. Preventive Services Task Force (USPSTF)
  An independent panel of experts in primary care and prevention that systematically reviews the evidence of effectiveness and develops recommendations for clinical preventive services.

Recommendations:

• Genetic Risk Assessment and BRCA Mutation Testing for Breast and Ovarian Cancer Susceptibility
• Screening for Colorectal Cancer
• Guide to Clinical Preventive Services, 2010 - 2011 (pocket guide)
Evidence Reports:

• Impact of Gene Expression Profiling Tests on Breast Cancer Outcomes
• Collection and Use of Cancer Family History in Primary Care?
• Enhancing Use and Quality of Colorectal Cancer Screening
• Family History and Improving Health
• Hereditary Nonpolyposis Colorectal Cancer: Diagnostic Strategies and Their Implications
• Genomic Tests for Ovarian Cancer Detection and Management

Cancer Genetics

• National Comprehensive Cancer Network Genetic/Familial High-Risk Assessment Guidelines
  The National Comprehensive Cancer Network (NCCN) is an alliance of multiple cancer centers that are working together to develop guidelines for cancer risk assessment and treatment. NCCN offers familial risk assessment for breast and/or ovarian and colorectal cancer.  (Requires registration; anyone can register)
• Genetics of Breast and Ovarian Cancer
  Information for health professionals created by the National Cancer Institute, National Institutes of Health.
• Oregon Comprehensive Cancer Control Program
  The Oregon Comprehensive Cancer Control Program includes a partnership plan with others commited to reducing the burden of cancer in Oregon. The Partnership is addressing objectives noted in the Oregon Comprehensive Cancer Plan including increasing the proportion of Oregonians who are aware of genetic factors that increase individual cancer risk.
• BRCA1 & BRCA2 Mutation Prevalence Tables
  Created by Myriad Genetic Laboratories, Inc.
• Familial Cancer Risk Assessment: Breast and Ovarian Cancer Powerpoint presentation, 2004
• Familial Cancer Risk Assessment: Colorectal Cancer Powerpoint presentation, 2004

Also see  Cancer Factsheets for public 

Diabetes and Family History

• Family History and Diabetes
  Powerpoint review for public health professionals, 2004.
• Genetics for Targeted Disease Prevention: Diabetes
  Journal article abstract provides an overview of current thinking regarding genetics and diabetes (type 1, type 2, and gestational diabetes mellitus), including a selective look at a few implicated variants, 2004.
• State of Oregon Diabetes Program
  The State of Oregon Diabetes Program's goal is to reduce the burden of diabetes in Oregon through a public health approach, working in collaboration with aprtners in the public and private sectors.

Also see Diabetes Factsheet(s) for public 

Preconception/Prenatal Genetic Screening

Materials were created through funding from the March of Dimes Oregon Chapter in 2004-2005.

• Prenatal Genetic Screening
  Powerpoint presentation
• Ethnicity-Based Genetic Carrier Screening
  Powerpoint presentation
• Maternal Serum Screening
  Powerpoint Presentation
• Preconception/Prenatal Family History Questionnaire
  March of Dimes

• Preconception/Prenatal Family History Assessment/Management Guide
  March of Dimes

Collecting and Using Family History

• All in the Family
  A resource (CD-Summary) for providers on ways of using family history to identify and prevent disease in high-risk populations.
   
• Sample Family Health History Form for Federally-Qualified Health Center
  Although originally created for Federally-Qualified Health Center (FQHC) providers in Oregon, this clinical template can be used to collect family history information from patients by any health care provider.

See  Family Health History page for more resources.

Health Care Provider Resources | Genetic Conditions