Australian journal of general practice · 2026
Integrating genomics into pre-pregnancy and pregnancy care in general practice: Practical tools from the PRECISE Project.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Gusen Talia, Makeham Meredith, Ma Alan, Bonakdar Tehrani Mehrnoush, Hayward Janette, Middleton Edwina, Chan Rebecca, Barnett Stephen
Аннотация
BACKGROUND: Genomic medicine is increasingly relevant in general practice. It supports more informed reproductive decision making and strengthens the way practitioners assess risk and guide patients through complex information.
OBJECTIVE: The aim of this article is to introduce tools and resources from the Practitioner Readiness, Education and Capabilities, with Implementation Science Evaluation (PRECISE) Project that help general practitioners offer genetic screening and counselling during pre-pregnancy and pregnancy. These resources aim to streamline assessment, improve communication and support consistent and efficient practice across settings.
DISCUSSION: The article describes how reproductive genetic carrier screening and non-invasive prenatal testing or screening fit into routine care. It highlights Continuing Professional Development-accredited modules, point-of-care guides and clear referral pathways that support confident use in busy clinics. It also outlines simple steps for discussing results, managing uncertainty and coordinating referrals to genetics services when required.
OBJECTIVE: The aim of this article is to introduce tools and resources from the Practitioner Readiness, Education and Capabilities, with Implementation Science Evaluation (PRECISE) Project that help general practitioners offer genetic screening and counselling during pre-pregnancy and pregnancy. These resources aim to streamline assessment, improve communication and support consistent and efficient practice across settings.
DISCUSSION: The article describes how reproductive genetic carrier screening and non-invasive prenatal testing or screening fit into routine care. It highlights Continuing Professional Development-accredited modules, point-of-care guides and clear referral pathways that support confident use in busy clinics. It also outlines simple steps for discussing results, managing uncertainty and coordinating referrals to genetics services when required.