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1.
Australas J Dermatol ; 2024 May 13.
Article in English | MEDLINE | ID: mdl-38741474

ABSTRACT

BACKGROUND: Treatment goals have been established in Australia to facilitate the management of adults with moderate to severe psoriasis. The Australasian College of Dermatologists sought to determine if and how these adult treatment goals could be modified to accommodate the needs of paediatric and adolescent patients. METHODS: A modified Delphi approach was used. Comprehensive literature review and guideline evaluation resulted in the development of statements and other questions to establish current clinical practices. Two rounds of anonymous voting were undertaken, with a collaborative meeting held in between to discuss areas of discordance. Overall, consensus was defined as achievement of ≥75% agreement in the range 7-9 on a 9-point scale (1 strongly disagree; 9 strongly agree). RESULTS: Consensus was achieved on 23/29 statements in round 1 and 17/18 statements in round 2. There was a high level of concordance with treatment criteria in the adult setting. The limitations of applying assessment tools developed for use in adult patients to the paediatric setting were highlighted. Treatment targets in the paediatric setting should include objective metrics for disease severity and psychological impact on the patients and their family, and be based on validated, age-appropriate tools. CONCLUSION: While the assessment, classification and management of moderate to severe psoriasis in paediatric patients aligns with metrics established for adults, it is vital that nuances in the transition from childhood to adolescence be taken into account. Future research should focus on psoriasis severity assessment scales specific to the paediatric setting.

3.
Australas J Dermatol ; 65(4): 373-377, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38445760

ABSTRACT

As with adults, paediatric patients may benefit from a number of advanced targeted therapies for inflammatory skin disease. This brief report aims to be an accessible reference tool with respect to regulatory approval and reimbursement of these treatments within Australia.


Subject(s)
Dermatologic Agents , Humans , Australia , Child , Dermatologic Agents/administration & dosage , Dermatologic Agents/therapeutic use , Psoriasis/drug therapy , Antibodies, Monoclonal, Humanized/therapeutic use , Antibodies, Monoclonal, Humanized/administration & dosage , Ustekinumab/therapeutic use , Ustekinumab/administration & dosage , Skin Diseases/drug therapy
4.
Australas J Dermatol ; 65(1): 59-62, 2024 Feb.
Article in English | MEDLINE | ID: mdl-37927148

ABSTRACT

There is increasing evidence of clinically resistant cutaneous fungal infections. The use of combination oral antifungals is described in adults but not in paediatric patients. We present seven paediatric cases of clinically resistant fungal infections treated successfully with combination oral antifungal therapy after inadequate response to a single agent.


Subject(s)
Antifungal Agents , Dermatomycoses , Child , Humans , Antifungal Agents/therapeutic use , Dermatomycoses/drug therapy , Administration, Oral
5.
J Paediatr Child Health ; 59(6): 851-852, 2023 06.
Article in English | MEDLINE | ID: mdl-37144960
6.
Australas J Dermatol ; 63(4): e289-e296, 2022 Nov.
Article in English | MEDLINE | ID: mdl-36057946

ABSTRACT

Discoid (nummular) eczema is a common and distinctive eczema variant, which has not been studied in depth. Although the principles of management are similar to that of classic atopic dermatitis, distinctions are made due to its unique presentation and persistent clinical course in children. Australian and New Zealand dermatologists with an interest in paediatric eczema developed a consensus narrative to assist clinicians in diagnosing and treating this subtype of eczema. Identifying triggers, potent topical corticosteroids under occlusion, skin barrier support and management of pruritus are first-line therapies, however, many eventually require systemic immunomodulatory agents.


Subject(s)
Dermatitis, Atopic , Dermatologic Agents , Eczema , Child , Humans , New Zealand , Australia , Eczema/diagnosis , Eczema/drug therapy , Dermatitis, Atopic/drug therapy , Dermatologic Agents/therapeutic use
8.
Australas J Dermatol ; 63(3): 365-367, 2022 Aug.
Article in English | MEDLINE | ID: mdl-35622930

ABSTRACT

Netherton syndrome is a rare, severe genetic disorder of cornification without specific treatment. We describe two cases who demonstrated marked cutaneous improvement with secukinumab and suggest a role for IL-17 therapy in treating this condition.


Subject(s)
Ichthyosis , Netherton Syndrome , Skin Neoplasms , Antibodies, Monoclonal, Humanized , Hair , Humans , Netherton Syndrome/complications , Netherton Syndrome/drug therapy
9.
Australas J Dermatol ; 62(4): 470-477, 2021 Nov.
Article in English | MEDLINE | ID: mdl-34523734

ABSTRACT

Baby wipes are a commonly used cleansing method for infants. A literature review has been performed to assess if using baby wipes is beneficial or harmful compared to water and cloth in terms of nappy rash. This includes a detailed analysis of baby wipe ingredients, as many skin irritants as well as allergens are identified. MedLine, Embase and PubMed were searched and after 420 titles and abstracts were screened, 21 studies remained for inclusion. Baby wipes are deemed as superior to water and cloth in the majority of the literature. However, no definitive conclusion can be drawn as many studies are also industry funded. The most notable allergens identified are fragrances, such as linalool, cocamidopropyl betaine (surfactant), formaldehyde-releasing preservatives and other preservatives, including methylisothiazolinone and methylchloroisothiazolinone. As not all allergens are listed on the label accurately, this can be misleading for the consumer.


Subject(s)
Diaper Rash/etiology , Household Products/adverse effects , Humans , Infant , Infant, Newborn , Perfume/adverse effects
13.
Australas J Dermatol ; 61(2): e158-e173, 2020 May.
Article in English | MEDLINE | ID: mdl-31721162

ABSTRACT

Probiotic supplementation may decrease the risk of allergic disease; however, there are differences between studies, such as the type of probiotic, the route or the duration of supplementation. Therefore, determining the most effective probiotic strain/s, route of administration and duration for clinical recommendation has been difficult. An electronic systematic literature search was undertaken between using Ovid MEDLINE, Embase, PubMed and Cochrane. Risk ratio (RR) and 95% confidence interval (CI) are presented for the studies. PEDro scale and Newcastle-Ottawa Scale were used to assess the quality of the included studies. A total of 21 studies met the inclusion criteria. Strain-specific sub-meta-analyses indicated that single strains are not as effective as probiotic mixtures and administration to a combination of pregnant mothers, breastfeeding mothers and infants had a reduced risk in the onset of atopic dermatitis in children. Our systematic review and meta-analysis showed that a mixture of probiotic supplementation given to the mother in pregnancy and continuing while breastfeeding and also to the infant in children classified as high-risk for atopic dermatitis and non-high-risk groups is the most efficacious in reducing the risk of incidence of atopic dermatitis in children.


Subject(s)
Breast Feeding/statistics & numerical data , Dermatitis, Atopic/prevention & control , Hypersensitivity, Immediate/prevention & control , Primary Prevention/methods , Probiotics/therapeutic use , Child , Eczema/prevention & control , Female , Humans , Infant , Pregnancy , Prenatal Care/methods , Rhinitis, Allergic/prevention & control
14.
Pediatr Dermatol ; 35(4): e221-e223, 2018 Jul.
Article in English | MEDLINE | ID: mdl-29683223

ABSTRACT

Mid-dermal elastolysis is an acquired skin condition affecting the elastin fibers of the dermis, resulting in laxity of the skin. We report a case of mid-dermal elastolysis for which novel treatment with mycophenolate mofetil was successful.


Subject(s)
Elastic Tissue/pathology , Enzyme Inhibitors/therapeutic use , Mycophenolic Acid/therapeutic use , Skin Diseases/drug therapy , Adolescent , Diagnosis, Differential , Female , Glucocorticoids/therapeutic use , Humans , Immunohistochemistry , Skin/pathology
15.
Australas J Dermatol ; 59(1): 31-40, 2018 Feb.
Article in English | MEDLINE | ID: mdl-27435804

ABSTRACT

BACKGROUND/OBJECTIVES: Systemic oral immunomodulators azathioprine, methotrexate and cyclosporin are widely used in paediatric dermatology. Routine blood tests are performed to minimise drug-related adverse events. However, the frequency of monitoring tests may lead to significant fearful experiences for patients. We reviewed haematological abnormalities and clinical side-effects in a paediatric clinic population commencing immunomodulators for dermatological conditions, where haematological profiles are monitored less frequently than in current recommendations. METHODS: A retrospective chart review of children started on azathioprine, methotrexate or cyclosporin for a dermatological condition between 2001-2015 from a primarily paediatric, private dermatology practice was performed. Blood tests were done at baseline, 1 month, 2 months and then 3-monthly for children on azathioprine. Children on methotrexate and cyclosporin had tests done at baseline, after 1 month and then 3-monthly. RESULTS: In total, 242 children were included in this study. Azathioprine, methotrexate and cyclosporin cohorts had 95, 97 and 50 patients treated for a mean duration of 656, 758 and 313 days, respectively. Isolated abnormal blood tests indicated the cessation of azathioprine in 3/95 (3%), methotrexate in 5/97 (5%) and cyclosporin in 2/50 (4%) of patients. Abnormal blood test results were not associated with any reported clinical side-effects in the azathioprine (P = 0.726), methotrexate (P = 0.06) or cyclosporin groups (P = 0.250). CONCLUSION: In our experience, less frequent monitoring did not result in any significant adverse events over a 15-year period. We suggest that haematological monitoring during immunosuppressants use can be safely reduced from current recommendations.


Subject(s)
Azathioprine/adverse effects , Cyclosporine/adverse effects , Drug Monitoring/standards , Immunosuppressive Agents/adverse effects , Methotrexate/adverse effects , Administration, Oral , Adolescent , Azathioprine/administration & dosage , Blood Cell Count , Child , Child, Preschool , Creatinine/blood , Cyclosporine/administration & dosage , Electrolytes/blood , Female , Humans , Immunoglobulin E/blood , Immunosuppressive Agents/administration & dosage , Liver Function Tests , Male , Methotrexate/administration & dosage , Methyltransferases/blood , Retrospective Studies , Skin Diseases/drug therapy , Urea/blood
18.
Australas J Dermatol ; 58(4): e171-e175, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28266703

ABSTRACT

The newly revised Australian Infant Feeding Guidelines recommends that all infants, including those at high risk of allergy, be introduced foods traditionally considered allergenic (such as peanut butter, dairy, wheat and egg) within the first year of life. High-risk infants are those with early onset eczema (<3-months old) or with moderate to severe eczema not responding to treatment (<6-months old). Eczema can also represent a symptom of allergy presentation and the recommended introduction of some foods in this group may lead to allergic reactions at home. Although there have been no reported deaths from gradual food introduction to infants at home and cohort studies have only reported mild to moderate reactions, there is anecdotal evidence that more severe reactions can occur rarely. Allergic reactions, even if they are not life-threatening, can be a terrifying experience for parents. Dermatologists play an important role when dealing with high-risk infants in promoting the message of early allergenic food introduction yet also instigating appropriate allergy testing when necessary. This short review aims to provide an update to Australasian dermatologists on the newly revised Australian Infant Feeding Guidelines and provide a food allergy screening pathway for high-risk infants prior to commencement of allergenic foods.


Subject(s)
Dermatology , Food Hypersensitivity/diagnosis , Food Hypersensitivity/etiology , Food/adverse effects , Australia , Eczema/complications , Food Hypersensitivity/prevention & control , Guidelines as Topic , Humans , Infant , Risk Factors , Skin Tests
19.
Australas J Dermatol ; 58(2): 155-159, 2017 May.
Article in English | MEDLINE | ID: mdl-28251611

ABSTRACT

Although most infantile haemangiomas do not require treatment due to a natural history of spontaneous involution, some require early intervention. The Australasian Vascular Anomalies Network and the Australasian Paediatric Dermatology Network have developed a consensus statement for the treatment of infantile haemangiomas with oral propranolol. Infants with haemangiomas that are life threatening, at risk of ulceration, or at risk of causing a significant functional impairment, psychological impact or physical deformity should be treated early with oral propranolol. Oral propranolol is safe and effective and in most healthy infants oral propranolol can be started in an outpatient setting.


Subject(s)
Consensus , Hemangioma, Capillary/drug therapy , Neoplastic Syndromes, Hereditary/drug therapy , Propranolol/therapeutic use , Vasodilator Agents/therapeutic use , Drug Monitoring , Humans , Patient Selection , Propranolol/administration & dosage , Vasodilator Agents/administration & dosage
20.
Australas J Dermatol ; 58(3): e138-e140, 2017 Aug.
Article in English | MEDLINE | ID: mdl-27641714

ABSTRACT

Benzalkonium chloride is a quaternary ammonium cationic detergent present in a number of household products, which can act as a major skin irritant. We present the case of six children who developed granular parakeratosis after exposure to benzalkonium chloride in laundry rinse aids, presenting as a brightly erythematous, tender but minimally pruritic, intertriginous eruption followed by superficial desquamation. The eruptions resolved over 3-4 weeks after cessation of exposure.


Subject(s)
Benzalkonium Compounds/adverse effects , Household Products/adverse effects , Parakeratosis/chemically induced , Parakeratosis/pathology , Adolescent , Child , Child, Preschool , Female , Humans , Laundering , Male
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