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. 2005 Jun 4;330(7503):1301–1302. doi: 10.1136/bmj.38398.590602.E0

Newly diagnosed HIV infections: review in UK and Ireland

Ann K Sullivan 1, Hilary Curtis 2, Caroline A Sabin 3, Margaret A Johnson 4
PMCID: PMC558202  PMID: 15894552

In 2001, 59% of people in the United Kingdom with HIV who were starting treatment had CD4 lymphocyte counts of fewer than 200 cells/μl,1 mostly because of late diagnosis. We investigated new HIV diagnoses in the UK and Ireland, to assess the occurrence of late diagnosis (CD4 lymphocyte count < 200 cells/μl) and associated features and to determine if patients had prior presentations that may have been related to HIV infection.

Participants, methods, and results

We did a national case review by sending structured questionnaire forms to adult HIV care providers in the United Kingdom and Ireland for patients presenting with a new diagnosis of HIV infection in January-March 2003 (maximum of 25 per centre). We collected information on clinical and immune status and hospital admissions and symptoms or conditions in the previous 12 months that might have been HIV related.

Of 148 centres, 113 (76%) responded with data on 977 patients. Overall, 301 (33%) presented late (table), and this was more common in older patients (adjusted odds ratio per increase in age group 1.68, 95% confidence interval 1.42 to 1.98; P = 0.0001) and in black Africans (1.66, 1.05 to 2.62, P = 0.03), but less likely in homosexual men, independent of age and ethnicity (0.63, 0.38 to 1.05, P = 0.07). Overall, 401 (41%) were diagnosed via routine screening; this was associated with being young, female, black African, and heterosexual; 664 (68%) were diagnosed in a genitourinary, sexual health, or HIV clinic, which was associated with being young, male, and homosexual, and less commonly associated with being black African. After adjusting for demographic factors (table) in a multivariable model, diagnosis as part of a routine screen and testing at a genitourinary, sexual health, or HIV clinic were both independently associated with a lower chance of late diagnosis (testing as part of routine screen 0.40, 0.29 to 0.55, P = 0.0001; testing at a clinic 0.60, 0.44 to 0.82, P = 0.001).

Table 1.

Patients presenting with a new diagnosis of HIV infection in January-March 2003 in the United Kingdom and Ireland. Values are numbers (percentages*) unless stated otherwise

Total With CD4 <200 cells/μl at presentation P value
No of patients 977 (100.0) 301 (33.4)
Sex:
Male
540 (55.4)
147 (29.9)
0.02
Female 434 (44.6) 152 (37.4)
Age (years):
15-19
21 (2.2)
3 (15.0)
<0.0001
20-29
312 (32.0)
67 (22.9)
30-39
444 (45.6)
145 (36.1)
40-49
153 (15.7)
65 (46.1)
50-59
32 (3.3)
14 (48.3)
≥60 12 (1.2) 5 (41.7)
Ethnic group:
White
320 (33.3)
70 (23.6)
<0.0001
Black African
576 (59.9)
209 (39.3)
Other 66 (6.9) 18 (30.5)
Risk group:
Heterosexual
660 (69.1)
225 (37.0)
0.0002
Homosexual
278 (29.1)
57 (22.2)
IDU/Other 17 (1.8) 8 (47.1)
CD4 count (cells/μl):
≤50
104 (11.6)
104 (100.0)
NA
51-200
197 (21.9)
197 (100.0)
201-350
232 (25.8)
0
351-500
179 (19.9)
0
>500
188 (20.9)
0
Not known 77
Viral load (copies/ml):
<500
49 (5.7)
10 (21.3)
<0.0001
500-10 000
209 (24.4)
25 (12.1)
10 000-30 000
144 (16.8)
27 (19.0)
30 000-100 000
202 (23.6)
77 (38.3)
≥100 000
251 (29.4)
133 (53.8)
Not known 122
US Centers for Disease Control stage:
A
560 (59.1)
82 (16.1)
<0.0001
B
245 (25.8)
96 (41.9)
C 143 (15.1) 116 (85.3)

NA=Not applicable.

*

Percentages are based on those with non-missing data (numbers with missing data for CD4 count and viral load are shown for information).

P values are from χ2 tests after excluding individuals with missing values.

In the year before HIV diagnosis, 168 patients (17%) had a clinical episode that was likely to be HIV related, including 58 hospital admissions (18 for tuberculosis). Data show that 35 subsequent hospital admissions may have been avoidable and that 160 patients who had experienced a clinical episode had a CD4 lymphocyte count below the threshold for initiating treatment according to British HIV Association guidelines,2 indicating that treatment may have been delayed.

Comment

We found a significant number of missed opportunities for earlier diagnosis of HIV infection with a high proportion of patients (17%) who sought medical care with symptoms in the preceding 12 months but remained undiagnosed. Many patients are not being diagnosed on routine screening, which accounted for less than half of the diagnoses, most of these occurring in sexual health clinics. This study provides further evidence of late diagnosis of HIV infection, reflecting national trends reported by the Health Protection Agency (www.hpa.org.uk). There are well recognised advantages, including public health and health cost benefits in addition to personal benefit to the patient, of early diagnosis of HIV and starting appropriate treatment with highly active antiretroviral therapy.3,4

To improve this situation, the proportion of people diagnosed as having HIV as part of routine screening needs to increase, with people at risk being encouraged to have an HIV test. Healthcare professionals' awareness of factors associated with late presentation of HIV infection and conditions likely to be related to HIV also need to increase. A wide range of healthcare providers are in a position to detect these HIV infections, because patients presented to a number of different locations with a wide variety of diseases and conditions. Improving the offering and uptake of HIV testing both as part of routine screening and as indicated by associated medical conditions should reduce the number of undiagnosed HIV infections.

What is already known on this topic

Many people with HIV in the UK are unaware of their status, possibly up to 30% of those infected

A substantial number of people are diagnosed as having HIV infection at a late stage of disease

What this study adds

Many patients are not having their HIV infection diagnosed on routine screening

Many patients present with advanced disease after initially presenting with HIV related symptoms but with their HIV infection remaining undiagnosed

See also p 1303

This article was posted on bmj.com on 13 May 2005: http://bmj.com/cgi/doi/10.1136/bmj.38398.590602.E0

The British HIV Association audit subcommittee comprises Brook G, Bunting P, Curtis H, de Ruiter A, DeSilva S, Freedman A, Johnson M (chair), McDonald C, Mital D, Monteiro E, Mulcahy F, O'Mahony C, Sabin C, Sullivan A, Tang A, Tudor-Williams G, Welch J, and Wilkins E.

Contributors: The audit subcommittee had the idea and designed the study. AKS, HC, and CAS collected and analysed the data. All the authors interpreted the data and wrote the manuscript. HC is guarantor.

Funding: British HIV Association. All authors are members of the association, and HC receives remuneration from the British HIV Association for coordinating this and similar studies

Competing interests: None declared.

Ethical approval: Not needed.

References

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  • 2.Pozniak A, Gazzard B, Anderson J, Babiker A, Churchill D, Collins S, et al. British HIV Association (BHIVA) guidelines for the treatment of HIV-infected adults with antiretroviral therapy. HIV Med 2003;4(suppl 1): S1-41. [PubMed] [Google Scholar]
  • 3.Palella FJ Jr, Deloria-Knoll M, Chmiel JS, Moorman AC, Wood KC, Greenberg AE, et al. Survival benefit of initiating antiretroviral therapy in HIV-infected persons in different CD4+ cell strata. Ann Intern Med 2003;138: 620-6. [DOI] [PubMed] [Google Scholar]
  • 4.Miners AH, Sabin CA, Trueman P, Youle M, Mocroft A, Johnson M, et al. Assessing the cost-effectiveness of HAART for adults with HIV in England. HIV Med 2001;2: 52-8. [DOI] [PubMed] [Google Scholar]

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