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1.
Sex Health ; 16(1): 56-62, 2019 02.
Article in English | MEDLINE | ID: mdl-30501846

ABSTRACT

Background Pre-exposure prophylaxis (PrEP) was introduced in Sexual Health Services of the Welsh National Health Service (NHS Wales) in July 2017 as a 3-year pilot service. METHODS: Data were collected through the pre-existing Sexual Health in Wales Surveillance System, to which codes were added to capture PrEP eligibility, outcome of offer of PrEP, reasons for declining and adherence. Eligibility categories were defined based on nationally agreed criteria: men who have sex with men (MSM) and transgender people at high risk of HIV acquisition; partners of HIV-positive individuals not known to be virally suppressed; and heterosexuals reporting condomless intercourse with a HIV-positive individual not known to be virally suppressed. RESULTS: During the first 6 months, 516 people were eligible, 96% of which were MSM. Overall, 57% of those eligible (296/516) started PrEP. Reasons for declining PrEP were given by 88 (56%) of 157 people; 50 (57%) of whom did not believe themselves to be at risk. Of the available adherence assessments, 89% considered that all risk episodes had been covered. Persistence at 3 months was assessed for 141 people, of which 93 (66%) were still using PrEP. There were no HIV diagnoses in people taking PrEP during the first 6 months. Twenty-nine people were diagnosed with 37 episodes of sexually transmissible infections (STIs) while on PrEP. STI incidence was 105.7 per 100 person-years. CONCLUSIONS: The early trend indicates that implementation of PrEP is progressing as planned, and the service has been utilised by clients. This analysis can help refine implementation, inform planning and research around uptake, use and effect in Wales and internationally.


Subject(s)
HIV Infections/prevention & control , Homosexuality, Male , Medication Adherence , Pre-Exposure Prophylaxis , Adolescent , Adult , Aged , Aged, 80 and over , Anti-HIV Agents/administration & dosage , Emtricitabine, Tenofovir Disoproxil Fumarate Drug Combination/administration & dosage , Female , Health Plan Implementation , Humans , Male , Middle Aged , National Health Programs , Pilot Projects , Program Evaluation , Sexual Partners , Transgender Persons , Wales/epidemiology , Young Adult
3.
Int J STD AIDS ; 29(11): 1120-1122, 2018 11.
Article in English | MEDLINE | ID: mdl-29665741

ABSTRACT

A 43-year-old Malaysian man with well-controlled HIV infection on combination antiretroviral therapy presented with a six-week history of a widespread rash. The patient was otherwise well but was developing new lesions on a daily basis. Referral to Dermatology instigated punch biopsies, which revealed a diagnosis of lymphomatoid papulosis type A. This case highlights the importance of swift referral, especially in cases of spontaneous regression of symptoms, in order to obtain the correct diagnosis. In most patients, this condition tends to be chronic, with its chronicity and benign clinical course setting it apart from cutaneous anaplastic T-cell lymphoma and Hodgkin's disease, which are major entities in the histological differential diagnosis.


Subject(s)
Exanthema/pathology , HIV Infections/complications , Lymphomatoid Papulosis/pathology , Skin Neoplasms/pathology , Adult , Antiretroviral Therapy, Highly Active , Biopsy , Exanthema/etiology , Female , HIV Infections/drug therapy , Humans
4.
Int J STD AIDS ; 27(10): 906-8, 2016 09.
Article in English | MEDLINE | ID: mdl-26384945

ABSTRACT

Trichomonas vaginalis is a sexually transmitted protozoan infection resulting in vulvo-vaginitis and altered vaginal discharge in symptomatic women. Trichomoniasis has been implicated in causing adverse pregnancy outcomes such as low birth weight and pre-term labour. Metronidazole is the recommended first-line treatment for trichomonal infection. Other nitroimidazoles, such as tinidazole, are used as alternative regimens with similar activity but at a greater expense. Treatment failure usually represents patient non-compliance or re-infection, although metronidazole resistance has previously been documented. Antimicrobial susceptibility testing for T. vaginalis is currently not available in the UK. Patients with disease unresponsive to first-line treatments pose a major challenge, as therapeutic options are limited. We present the case of a patient with presumed resistant infection during pregnancy, and the additional treatment issues that this presented.


Subject(s)
Antitrichomonal Agents/therapeutic use , Metronidazole/therapeutic use , Pregnancy Complications, Parasitic/drug therapy , Tinidazole/therapeutic use , Trichomonas Vaginitis/drug therapy , Trichomonas vaginalis/isolation & purification , Drug Resistance , Female , Humans , Pregnancy , Pregnancy Complications, Parasitic/diagnosis , Pregnancy Outcome , Treatment Outcome , Trichomonas Vaginitis/diagnosis , Trichomonas vaginalis/drug effects
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