Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20042
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dc.contributor.authorHamblin, Peter S-
dc.contributor.authorSheehan, Penelope M-
dc.contributor.authorAllan, Carolyn-
dc.contributor.authorHoulihan, Christine A-
dc.contributor.authorLu, Zhong X-
dc.contributor.authorForehan, Simon P-
dc.contributor.authorTopliss, Duncan J-
dc.contributor.authorGilfillan, Christopher-
dc.contributor.authorKrishnamurthy, Bala-
dc.contributor.authorRenouf, Debra-
dc.contributor.authorSztal-Mazer, Shoshana-
dc.contributor.authorVaradarajan, Suresh-
dc.date2018-12-18-
dc.date.accessioned2019-01-02T01:15:10Z-
dc.date.available2019-01-02T01:15:10Z-
dc.date.issued2019-
dc.identifier.citationInternal Medicine Journal 2019; 49(8): 994-1000en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20042-
dc.description.abstractInterest in potential adverse outcomes associated with maternal subclinical hypothyroidism (normal Free T4, elevated TSH) has increased significantly over recent years. In turn, the frequency of maternal thyroid function testing has risen, despite universal thyroid function screening not being recommended, leading to a marked increase in referrals to obstetric endocrinology clinics. In 2017 the American Thyroid Association (ATA) revised their diagnostic and management guidelines. While welcome, these new guidelines contain recommendations which may cause confusion in clinical practice. To ensure uniform practice in the diagnosis and management of subclinical hypothyroidism in pregnancy across all Melbourne Public Hospitals. Consensus was achieved and the guidelines were endorsed by the Council of the Endocrine Society of Australia. Trimester and assay specific TSH reference intervals derived from healthy local populations should be used, where available. When unavailable, a TSH cut-off of 4 mU/L (replacing the previously recommended 2.5 mU/L) should be used to initiate treatment, irrespective of thyroid autoantibody status. The recommended starting dose of levothyroxine is 50 ug daily, with a therapeutic TSH target of 0.1 mU/L to 2.5 mU/L. Levothyroxine should generally be ceased after delivery, with some exceptions. Hospitals will ensure smooth transfer of care back to the woman's general practitioner with clear documentation of pregnancy thyroid management and a recommended plan for follow-up. Fewer women will be classified as having subclinical hypothyroidism during pregnancy, which is likely to lead to reductions in emotional stress, hospital visits, repeated blood tests and financial costs. Uniform clinical practice will occur across Melbourne. This article is protected by copyright. All rights reserved.en_US
dc.language.isoeng-
dc.subjectHypothyroidismen_US
dc.subjectPregnancyen_US
dc.subjectSubclinical hypothyroidismen_US
dc.titleSubclinical Hypothyroidism During Pregnancy: The Melbourne Public Hospitals Consensus.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleInternal Medicine Journalen_US
dc.identifier.affiliationPeninsula Clinical School, Monash University, Frankston, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Endocrinology & Diabetes, Eastern Health, Box Hill, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, Eastern Clinical School, Monash University, Box Hill, Victoria, Australiaen_US
dc.identifier.affiliationWerribee Mercy Hospital, 300 Princes Highway, Werribee, Victoria, Australiaen_US
dc.identifier.affiliationSt Vincents Institute of Medical Research, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Endocrinology & Diabetes, Peninsula Health, Frankston, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Endocrinology & Diabetes, Western Health, Sunshine Hospital, 176 Furlong Road, St Albans 3021en_US
dc.identifier.affiliationDepartment of Medicine - Western Precinct, The University of Melbourne, St Albans, VIC, 3021en_US
dc.identifier.affiliationPregnancy Research Centre, Royal Women's Hospital, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationUniversity of Melbourne Department of Obstetrics & Gynaecology, Royal Women's Hospital, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationEndocrine Services in Pregnancy, Monash Health, Clayton, Victoria, Australiaen_US
dc.identifier.affiliationHudson Institute of Medical Research Clayton, Victoria, Australiaen_US
dc.identifier.affiliationMercy Hospital for Women, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationAustin Healthen_US
dc.identifier.affiliationDepartment of Chemical Pathology, Melbourne Pathology, Collingwood, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, Monash University, Clayton, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Endocrinology & Diabetes, The Alfred, Commercial Road, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Medicine, Central Clinical School, Monash University, The Alfred, Commercial Road Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Diabetes and Endocrinology, Royal Melbourne Hospital, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationDepartment of Endocrinology & Diabetes, Northern Health, Epping, Victoria, Australiaen_US
dc.identifier.doi10.1111/imj.14210en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-6280-865Xen_US
dc.identifier.pubmedid30561039-
dc.type.austinJournal Article-
local.name.researcherHoulihan, Christine A
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptEndocrinology-
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