Summary. Objective: A quality improvement (QI) strategy to improve the rate of genetic counseling (GC) services was initiated in cystic fibrosis (CF) care Center E in 2010. This state-wide study was conducted to determine: (1) GC rates before and after implementation of the QI strategy at Center E; (2) characteristics associated with not receiving GC; and (3) topic areas addressed during GC. Methods: The retrospective study included 1,097 CF carriers born from 2008 to 2011 identified through Michigan’s Newborn Screening Program. Rate of GC services was determined for Center E and the other four CF centers before and after the QI change. Bivariate and multivariable logistic regression was used to determine associations between select charact...
Introduction: Cystic fibrosis is considered the most common autosomal disease with multisystem compl...
This paper presents results from a 1991 OTA survey of 431 genetic counselors and nurse geneticists. ...
OBJECTIVES: To determine whether the improved clinical status after newborn screening (NBS) for cyst...
PURPOSE: To study the follow-up of genetic counseling performed in families with a newborn detected ...
AbstractBackgroundThere is no valid and reliable instrument to evaluate genetic education and counse...
Background: Although cystic fibrosis (CF) is a common genetic condition, genetic counselling service...
Our objective was to describe: 1) physicians’ knowledge of whether genetic counseling is provided to...
OBJECTIVE: To evaluate compliance with recommendations for sweat testing/specialty evaluation and ge...
Many patients with cystic fibrosis (CF) are living well into their adult years and contemplating par...
Cystic fibrosis (CF) care has rapidly evolved over the past decade due to the introduction of CFTR m...
AUTOMATIC REFERRALS WITHIN A CYSTIC FIBROSIS MULTIDISCIPLINARY CLINIC IMPROVE PATIENT EVALUATION AND...
International audienceWhile the goals of genetic counseling for cystic fibrosis - delivering relevan...
Cystic fibrosis (CF) newborn screening (NBS) was universally adopted in 2009 in the United States. V...
Genetic testing and genetic counseling are crucial components of the growing Precision Medicine init...
Background: The Cystic Fibrosis (CF) Registry collects clinical data on all patients attending speci...
Introduction: Cystic fibrosis is considered the most common autosomal disease with multisystem compl...
This paper presents results from a 1991 OTA survey of 431 genetic counselors and nurse geneticists. ...
OBJECTIVES: To determine whether the improved clinical status after newborn screening (NBS) for cyst...
PURPOSE: To study the follow-up of genetic counseling performed in families with a newborn detected ...
AbstractBackgroundThere is no valid and reliable instrument to evaluate genetic education and counse...
Background: Although cystic fibrosis (CF) is a common genetic condition, genetic counselling service...
Our objective was to describe: 1) physicians’ knowledge of whether genetic counseling is provided to...
OBJECTIVE: To evaluate compliance with recommendations for sweat testing/specialty evaluation and ge...
Many patients with cystic fibrosis (CF) are living well into their adult years and contemplating par...
Cystic fibrosis (CF) care has rapidly evolved over the past decade due to the introduction of CFTR m...
AUTOMATIC REFERRALS WITHIN A CYSTIC FIBROSIS MULTIDISCIPLINARY CLINIC IMPROVE PATIENT EVALUATION AND...
International audienceWhile the goals of genetic counseling for cystic fibrosis - delivering relevan...
Cystic fibrosis (CF) newborn screening (NBS) was universally adopted in 2009 in the United States. V...
Genetic testing and genetic counseling are crucial components of the growing Precision Medicine init...
Background: The Cystic Fibrosis (CF) Registry collects clinical data on all patients attending speci...
Introduction: Cystic fibrosis is considered the most common autosomal disease with multisystem compl...
This paper presents results from a 1991 OTA survey of 431 genetic counselors and nurse geneticists. ...
OBJECTIVES: To determine whether the improved clinical status after newborn screening (NBS) for cyst...