CLINICAL GUIDELINES GENETIC TESTING

AIM General Clinical Guideline

OPEN THE GENERAL CLINICAL GUIDELINE EFFECTIVE AUGUST 17, 2020

AIM CLINICAL APPROPRIATENESS GUIDELINES FOR GENETIC TESTING

The foundation of our solution platform for specialty benefits management is our clinical appropriateness guidelines. AIM Clinical Appropriateness Guidelines for Genetic Testing are developed through a rigorous process integrating evidence-based literature with expert review.

 

AIM CLINICAL APPROPRIATENESS GUIDELINES FOR GENETIC TESTING FOR HEREDITARY CARDIAC DISEASE

The testing addressed in the AIM Clinical Appropriateness Guidelines for Genetic Testing for Hereditary Cardiac Disease includes testing for inherited arrhythmias and cardiomyopathies.

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AIM CLINICAL APPROPRIATENESS GUIDELINES FOR GENETIC TESTING FOR HEREDITARY CANCER SUSCEPTIBILITY

The testing addressed in the AIM Clinical Appropriateness Guidelines for Genetic Testing for Hereditary Cancer Susceptibility includes screening for hereditary cancer predisposition syndromes.

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COMING SOON HEREDITARY CANCER SUSCEPTIBILITY GUIDELINES EFFECTIVE JANUARY 4, 2021

 

AIM CLINICAL APPROPRIATENESS GUIDELINES FOR MOLECULAR TESTING OF SOLID AND HEMATOLOGIC TUMORS AND MALIGNANCIES

The testing addressed in the AIM Clinical Appropriateness Guidelines for Molecular Testing of Solid and Hematologic Tumors and Malignancies includes genetic testing and gene expression profiling of solid and hematologic tumors for the purpose of diagnosis or for information related to treatment selection, prognosis, or recurrence risks.

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COMING SOON MOLECULAR TESTING OF SOLID AND HEMATOLOGIC TUMORS AND MALIGNANCIES GUIDELINES EFFECTIVE JANUARY 4, 2021

 

AIM CLINICAL APPROPRIATENESS GUIDELINES FOR PHARMACOGENETIC TESTING AND GENETIC TESTING FOR THROMBOTIC DISORDERS

The testing addressed in the AIM Clinical Appropriateness Guidelines for Pharmacogenetic Testing and Genetic Testing for Thrombotic Disorders includes genotyping to predict response to certain medications and testing for gene mutations associated with coagulation disorders.

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AIM CLINICAL APPROPRIATENESS GUIDELINES FOR GENETIC TESTING FOR SINGLE-GENE AND MULTIFACTORIAL CONDITIONS

The testing addressed in the AIM Clinical Appropriateness Guidelines for Genetic Testing for Single-Gene and Multifactorial Conditions includes single-gene testing, multigene diagnostic panels, testing for variants associated with multifactorial conditions, chromosomal microarray analysis, and human leukocyte antigen (HLA) histocompatibility testing.

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AIM CLINICAL APPROPRIATENESS GUIDELINES FOR WHOLE EXOME AND WHOLE GENOME SEQUENCING

The testing addressed in the AIM Clinical Appropriateness Guidelines for Whole Exome and Whole Genome Sequencing includes the diagnostic use of whole exome and genome sequencing in the evaluation of rare disease.

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AIM CLINICAL APPROPRIATENESS GUIDELINES FOR GENETIC TESTING FOR REPRODUCTIVE CARRIER SCREENING AND PRENATAL DIAGNOSIS

The testing addressed in the AIM Clinical Appropriateness Guidelines for Genetic Testing for Reproductive Carrier Screening and Prenatal Diagnosis includes carrier testing for familial mutations and common and ethnic genetic diseases; preimplantation screening and diagnosis; prenatal screening and diagnosis; and testing for recurrent pregnancy loss and infertility.

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COMING SOON REPRODUCTIVE CARRIER SCREENING AND PRENATAL DIAGNOSIS GUIDELINES EFFECTIVE JANUARY 4, 2021

 

Guidelines developed by, and used with permission from, Informed Medical Decisions, Inc. (dba InformedDNA®). © 2020 Informed Medical Decisions, Inc. All rights reserved.

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