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Review of services for people living with HIV in New Zealand

Review of services for people living with HIV in New Zealand

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It is evident that stigma is the elephant <strong>in</strong> the wait<strong>in</strong>g room <strong>of</strong> <strong>HIV</strong> public health responses – <strong>of</strong>ten<strong>in</strong>voked as the cause <strong>of</strong> sub‐optimal population responses to prevention and support activities, yethard to quantify or isolate by region or population.There is some debate over how best to engage m<strong>in</strong>ority populations (and, correspond<strong>in</strong>gly, who isthe preferred service provider). One side <strong>of</strong> the argument is that a ‘by Māori <strong>for</strong> Māori’ (or a ‘byAfricans <strong>for</strong> Africans’) approach is necessary to ensure the quality <strong>of</strong> engagement <strong>with</strong> those most atrisk that would guarantee susta<strong>in</strong>ed, effective <strong>HIV</strong>/STI prevention and care. The other side suggeststhat the equal access guaranteed by current DHB and NGO <strong>services</strong> <strong>of</strong>fers a greater degree <strong>of</strong>anonymity and confidentiality that is crucial. In other words, the impact <strong>of</strong> stigma differentiateshealth care delivery <strong>for</strong> <strong>HIV</strong> and SH from that <strong>of</strong> other conditions. One physician noted, ‘We are bestplaced to deliver [to m<strong>in</strong>ority ethnic populations] because <strong>of</strong> our place <strong>with</strong><strong>in</strong> the health serviceculture.’ Another noted that the presence <strong>of</strong> health providers outside traditional family andcommunity networks encouraged engagement <strong>of</strong> some <strong>people</strong> <strong>with</strong> SH <strong>services</strong> cit<strong>in</strong>g the maxim, ashas been quoted elsewhere, ‘you don’t know my auntie’.The strength <strong>of</strong> the arguments on both sides is tempered by the limited data available <strong>for</strong> clarify<strong>in</strong>gthem. One example is the question over whether populations <strong>of</strong> Māori, or <strong>of</strong> Africans, andconsequently their responses to <strong>HIV</strong> at an <strong>in</strong>dividual and community level, are homogenous. Manystaff and PLHA asserted that they were not, and questioned public health responses rely<strong>in</strong>g onhomogeneity as an assurance <strong>of</strong> expected ethnic responses. The experiences <strong>of</strong> Māori and Africancommunity personnel employed by the NZAF and DHBs have been difficult to accurately evaluatebecause <strong>of</strong> <strong>in</strong>dividuals’ <strong>of</strong>ten reported fear <strong>of</strong> disclos<strong>in</strong>g their <strong>HIV</strong> status <strong>with</strong><strong>in</strong> their communities,either <strong>in</strong> or outside <strong>New</strong> <strong>Zealand</strong>. The power <strong>of</strong> this fear is doubtless compounded by the sense <strong>of</strong>vulnerability that is consistently reported among immigrant populations. It was also acknowledgedthat there was comparatively little literature focussed on Māori or African issues <strong>in</strong> SH.Research <strong>in</strong>to ‘conventional’ STIs <strong>of</strong>fers a start<strong>in</strong>g po<strong>in</strong>t <strong>for</strong> assessment <strong>of</strong> such issues. The recentchlamydia study undertaken <strong>in</strong> the Waikato (Morgan and Bell 2009), identified that equitable accessto <strong>services</strong> was not an issue among Māori populations. In this study, Māori were as likely to betested <strong>for</strong> chlamydia, but were twice as likely as non‐Māori to test positive. Look<strong>in</strong>g at patterns <strong>of</strong>test<strong>in</strong>g <strong>in</strong> the various provider locations surveyed seems to suggest that equity <strong>of</strong> access had beenachieved through <strong>in</strong>itiatives to ensure access to free sexual and reproductive health <strong>services</strong> <strong>for</strong> allunder‐25s <strong>with</strong><strong>in</strong> the district. A Waikato DHB case management audit <strong>of</strong> 415 cases, 41 percent <strong>of</strong>which were Māori, found that time between diagnosis and treatment follow<strong>in</strong>g a positive chlamydiaresult was equitable. However, a small number <strong>with</strong> untreated <strong>in</strong>fections were more likely to beMāori than non‐Māori.The Hamilton SH cl<strong>in</strong>ic (who noted that ‘we only have data from <strong>people</strong> who come <strong>in</strong> to <strong>services</strong>’)reported that attendance is <strong>in</strong>fluenced by both perception <strong>of</strong> service staff competency and bywhether such <strong>services</strong> are free or not. This study found that <strong>in</strong> general access was more affected bysocioeconomic aspects than by ethnicity. This is consistent <strong>with</strong> the request from groups <strong>of</strong> serviceusers<strong>for</strong> <strong>HIV</strong> specialist <strong>services</strong> to provide essential primary care‐type functions, because <strong>of</strong> theprohibitive costs <strong>of</strong> primary care.While most adults are registered <strong>with</strong> a primary care practice, and at least 90 percent see theirprimary care physician at least once a year, data suggests this figure may be lower among those mostat risk <strong>of</strong> STIs and <strong>HIV</strong>. For example, primary care data suggests that only 60 percent <strong>of</strong> 15–24 yearoldsare engaged <strong>with</strong> a primary care physician. Also, recent data suggests that MSM <strong>of</strong>ten do notdisclose sexuality to their general practitioners (Adams, McCreanor and Braun 2008).REVIEW OF SERVICES FOR PLHA 41

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