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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chew C.Y. | en |
dc.contributor.author | Saracino A.M. | en |
dc.contributor.author | Nikpour M. | en |
dc.contributor.author | Mar A. | en |
dc.date.accessioned | 2021-05-14T11:57:01Z | en |
dc.date.available | 2021-05-14T11:57:01Z | en |
dc.date.copyright | 2020 | en |
dc.date.created | 20200605 | en |
dc.date.issued | 2020-06-05 | en |
dc.identifier.citation | Australasian Journal of Dermatology. 61 (2) (pp e150-e157), 2020. Date of Publication: 01 May 2020. | en |
dc.identifier.issn | 0004-8380 | en |
dc.identifier.uri | https://repository.monashhealth.org/monashhealthjspui/handle/1/35375 | en |
dc.description.abstract | Hydroxychloroquine is an age-old drug whose use as an immunomodulatory agent with a low side-effect profile continues to expand. We present a review of this drug including recently updated prescribing recommendations and a summary of its clinical application in dermatology. A maximum daily dose of 5.0 mg/kg based on actual body weight and no greater than 400 mg is advised in order to reduce the risk of retinopathy, which is potentially permanent and has an estimated prevalence of 7.5% at 5 years on standard dosing. Baseline ophthalmologic assessment followed by annual screening after 5 years is recommended; however, closer monitoring should be considered in the setting of existing retinopathy, a cumulative dose > 1000 g or renal dysfunction. Hydroxychloroquine is now considered to be safe in pregnancy, and routine glucose-6-phosphate dehydrogenase (G6PD) deficiency testing is not required. Smoking can significantly decrease its efficacy although the reason is still uncertain. Hydroxychloroquine appears to also demonstrate antineoplastic and cardioprotective benefits.Copyright © 2019 The Australasian College of Dermatologists | en |
dc.language | en | en |
dc.language | English | en |
dc.publisher | Blackwell Publishing | en |
dc.relation.ispartof | Australasian Journal of Dermatology | en |
dc.subject.mesh | drug absorption | - |
dc.subject.mesh | drug bioavailability | - |
dc.subject.mesh | drug contraindication | - |
dc.subject.mesh | drug efficacy | - |
dc.subject.mesh | drug metabolism | - |
dc.subject.mesh | drug safety | - |
dc.subject.mesh | erythema annulare centrifugum | - |
dc.subject.mesh | erythema multiforme | - |
dc.subject.mesh | eye examination | - |
dc.subject.mesh | gastrointestinal symptom | - |
dc.subject.mesh | giant cell granuloma | - |
dc.subject.mesh | glioblastoma | - |
dc.subject.mesh | glucose 6 phosphate dehydrogenase deficiency | - |
dc.subject.mesh | granuloma annulare | - |
dc.subject.mesh | heart protection | - |
dc.subject.mesh | heartburn | - |
dc.subject.mesh | hyperpigmentation | - |
dc.subject.mesh | hypertransaminasemia | - |
dc.subject.mesh | hypoglycemia | - |
dc.subject.mesh | immunomodulation | - |
dc.subject.mesh | irritability | - |
dc.subject.mesh | leukopenia | - |
dc.subject.mesh | lichen (disease) | - |
dc.subject.mesh | lichen planus | - |
dc.subject.mesh | lichen sclerosus et atrophicus | - |
dc.subject.mesh | liver toxicity | - |
dc.subject.mesh | lung cancer | - |
dc.subject.mesh | lupus vulgaris | - |
dc.subject.mesh | measles like rash | - |
dc.subject.mesh | melanoma | - |
dc.subject.mesh | mood change | - |
dc.subject.mesh | morphea | - |
dc.subject.mesh | mucinosis | - |
dc.subject.mesh | multiple myeloma | - |
dc.subject.mesh | nausea | - |
dc.subject.mesh | necrobiosis lipoidica | - |
dc.subject.mesh | nightmare | - |
dc.subject.mesh | pancreas cancer | - |
dc.subject.mesh | panniculitis | - |
dc.subject.mesh | patient monitoring | - |
dc.subject.mesh | pharmacodynamics | - |
dc.subject.mesh | photodermatosis | - |
dc.subject.mesh | porphyria cutanea tarda | - |
dc.subject.mesh | practice guideline | - |
dc.subject.mesh | pregnancy | - |
dc.subject.mesh | prescription | - |
dc.subject.mesh | pruritus | - |
dc.subject.mesh | psoriasis | - |
dc.subject.mesh | rash | - |
dc.subject.mesh | retina maculopathy | - |
dc.subject.mesh | retinopathy | - |
dc.subject.mesh | risk benefit analysis | - |
dc.subject.mesh | risk reduction | - |
dc.subject.mesh | sarcoma | - |
dc.subject.mesh | skin contusion | - |
dc.subject.mesh | skin sarcoidosis | - |
dc.subject.mesh | smoking | - |
dc.subject.mesh | solid malignant neoplasm | - |
dc.subject.mesh | Stevens Johnson syndrome | - |
dc.subject.mesh | systemic lupus erythematosus | - |
dc.subject.mesh | systemic sclerosis | - |
dc.subject.mesh | toxic epidermal necrolysis | - |
dc.subject.mesh | urticaria | - |
dc.subject.mesh | vasculitis | - |
dc.subject.mesh | visual impairment | - |
dc.subject.mesh | vomiting | - |
dc.subject.mesh | cyclosporine/it [Drug Interaction] | - |
dc.subject.mesh | digoxin/it [Drug Interaction] | - |
dc.subject.mesh | glucose 6 phosphate dehydrogenase | - |
dc.subject.mesh | hydroxychloroquine [Adverse Drug Reaction] | - |
dc.subject.mesh | hydroxychloroquine/it [Drug Interaction] | - |
dc.subject.mesh | hydroxychloroquine | - |
dc.subject.mesh | methotrexate/it [Drug Interaction] | - |
dc.subject.mesh | follicular mucinosis | - |
dc.subject.mesh | lichen planopilaris | - |
dc.subject.mesh | reticular erythematous mucinosis | - |
dc.subject.mesh | urticarial vasculitis | - |
dc.subject.mesh | laboratory test | - |
dc.subject.mesh | abdominal distension | - |
dc.subject.mesh | acute generalized exanthematous pustulosis | - |
dc.subject.mesh | agranulocytosis | - |
dc.subject.mesh | alopecia | - |
dc.subject.mesh | alopecia areata | - |
dc.subject.mesh | anorexia | - |
dc.subject.mesh | antineoplastic activity | - |
dc.subject.mesh | antiphospholipid syndrome | - |
dc.subject.mesh | antithrombotic activity | - |
dc.subject.mesh | aplastic anemia | - |
dc.subject.mesh | blood toxicity | - |
dc.subject.mesh | chronic urticaria | - |
dc.subject.mesh | dermatology | - |
dc.subject.mesh | dermatomyositis | - |
dc.subject.mesh | diarrhea | - |
dc.subject.mesh | DRESS syndrome | - |
dc.title | Hydroxychloroquine in dermatology: New perspectives on an old drug. | en |
dc.type | Review | en |
dc.identifier.affiliation | Dermatology | - |
dc.type.studyortrial | Review article (e.g. literature review, narrative review) | - |
dc.identifier.doi | http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1111/ajd.13168 | - |
dc.publisher.place | Australia | en |
dc.identifier.pubmedid | 31612996 [http://www.ncbi.nlm.nih.gov/pubmed/?term=31612996] | en |
dc.identifier.source | 2003501174 | en |
dc.identifier.institution | (Chew, Mar) Department of Dermatology, Monash Health, Clayton, VIC, Australia (Nikpour) The University of Melbourne at St. Vincent's Hospital Melbourne, Melbourne, VIC, Australia (Saracino) Division of Medicine, Centre for Rheumatology and Connective Tissue Diseases, University College London at Royal Free Hospital London, London, United Kingdom | en |
dc.description.address | A.M. Saracino, Division of Medicine, Centre for Rheumatology and Connective Tissue Diseases, University College London at Royal Free Hospital London, London, United Kingdom. E-mail: amanda.saracino.15@ucl.ac.uk | en |
dc.description.publicationstatus | Embase | en |
dc.rights.statement | Copyright 2020 Elsevier B.V., All rights reserved. | en |
dc.subect.keywords | adverse effects dermatology hydroxychloroquine lupus erythematosus monitoring plaquenil recommendations retinopathy | en |
dc.identifier.authoremail | Saracino A.M.; amanda.saracino.15@ucl.ac.uk | en |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.openairetype | Review | - |
crisitem.author.dept | Dermatology | - |
Appears in Collections: | Articles |
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