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Erschienen in: BMC Infectious Diseases 1/2018

Open Access 01.12.2018 | Research article

“Late for testing, early for antiretroviral therapy, less likely to die”: results from a large HIV cohort study in China, 2006–2014

verfasst von: Houlin Tang, Yurong Mao, Weiming Tang, Jing Han, Juan Xu, Jian Li

Erschienen in: BMC Infectious Diseases | Ausgabe 1/2018

Abstract

Background

Timely HIV testing and initiation of antiretroviral therapy are two major determinants of survival for HIV-infected individuals. Our study aimed to explore the trend of late HIV/AIDS diagnoses and to assess the factors associated with these late diagnoses in China between 2006 and 2014.

Methods

We used data from the Chinese Comprehensive Response Information Management System of HIV/AIDS (CRIMS). All individuals who tested positive for HIV between 2006 and 2014 in China and were at least 15 years of age were included. A late diagnosis was defined as an instance in which an individual was diagnosed as having AIDS or WHO stage 3 or 4 HIV/AIDS, or had a CD4 cell count less than 200 cells/mm3 at the time of diagnosis.

Results

Among the 528,234 individuals (≥15 years old) newly diagnosed with HIV between 2006 and 2014, 179,700 (34.0%) people were considered to have received late diagnoses. The late diagnosis rate decreased from 33.9% in 2006 to 29.7% in 2014 (P < 0.01). Late diagnoses were more likely to be found among those who were 45–54 years old (adjusted odds ratio [aOR]: 3.25, 95% confidence interval [CI]: 3.17–3.34) or 55+ years old (OR: 2.94, 95% CI: 2.86–3.02), male (aOR: 1.15, 95% CI: 1.13,1.17), employed as a farmer or rural laborer (aOR: 1.13, 95% CI: 1.11–1.14), infected through blood or plasma transfusion (aOR: 4.18, 95% CI: 4.02, 4.35), diagnosed at hospitals (OR: 1.17, 95% CI: 1.15, 1.19), of Han ethnicity (aOR: 1.30, 95% CI: 1.28, 1.32), and married (OR: 1.12, 95% CI: 1.11,1.13). Of those people living with HIV (PLHIV) who received late diagnoses, 7.4%(8637) and 46.1%(28,462) ultimately died with or without receiving antiretroviral therapy within a year of diagnosis, respectively.

Conclusion

A large proportion of individuals with HIV/AIDS receive late diagnoses, and this proportion has witnessed a slight decline in recent years. Expanded testing is needed to increase early HIV diagnosis and antiretroviral therapy should be recommended to all diagnosed individuals as early as possible to reduce AIDS-related death.
Abkürzungen
ART
Antiretroviral Therapy
CBOs
Community Based Organizations
CDC
Centre for Disease Control and Prevention
CRIMS
Chinese Comprehensive Response Information Management System of HIV/AIDS
HAART
Highly active antiretroviral therapy
HIV
Human Immunodeficiency Virus
MMT
Methadone Maintenance Treatment
MSM
Men Who Have Sex with Men
NCAIDS
National Centre for AIDS/STD Control and Prevention
NCRD
National Case Reporting Database
NFATD
National Free Antiretroviral Therapy Database
OR
Odds Ratio
PITC
Provider-Initiated HIV Testing and Counseling
PLHIV
People Living with HIV
VCT
Voluntary Counseling and Testing

Background

The introduction and expansion of highly active antiretroviral therapy (HAART) has proven to be one of the most remarkable public health measures in reducing the morbidity and mortality caused by the Human Immunodeficiency Virus (HIV) [14]. UNAIDS sets an ambitious treatment target to help end the AIDS epidemic: By 2020, 90% of all people living with HIV know their HIV status, 90% of people with diagnosed HIV receive antiretroviral therapy (ART) and 90% of all people on HIV treatment achieve viral suppression [5]. However, delayed testing as well as stigma and discrimination against infected individuals places them at risk of receiving delayed antiretroviral therapy [6].
Early detection of HIV infection is a critical factor in controlling the spread of HIV [7]. Timely ART is associated with a better prognosis among HIV-infected individuals and lower rates of disease progression [8]. Prompt linkages with health care systems at the start of ART yields the maximum benefits of HIV medical treatment for people living with HIV (PLHIV) [9] while decreasing the sexual transmission rate of HIV [1013]. A late diagnosis is detrimental to both the individual infected with HIV and the community for two reasons. First, in the absence of timely initiation of ART, the majority of patients will suffer the deleterious effects of HIV infection due to the gradual failure of the immune system, ranging from infection by opportunistic diseases to even death. Second, the propensity for HIV transmission by untested and hence unaware PLHIV is greater [14, 15] than for those made aware of their HIV status.
Developed countries such as the USA, Canada, and the European Union have been successful in addressing some of the key operational factors hindering the effective management of diseases affecting PLHIV [1621]. However, it is estimated that 30% of PLHIV in the European Union [9] remain undiagnosed, while evidence from the United States suggests that 25% of the undiagnosed population is responsible for the transmission of new HIV infections in 54% of cases [7, 22].
The proportion of those who received late diagnoses in industrialized countries is most often reported at between 25 and 45% of all newly HIV-diagnosed cases [23]. Though the largest proportion of undiagnosed PLHIV resides in developing countries, little research describing their characteristics has been conducted in these settings. In China, HIV voluntary counseling and testing (VCT) is free and can be widely accessed in urban areas. However, this free testing strategy has not been able to prevent a large proportion of cases of late HIV diagnosis for several reasons [24]. Incomplete HIV screening among STD patients in China has been cited as one important cause of missed opportunities for HIV testing [25].
Our study aimed to identify characteristics and trends of cases of late HIV/AIDS diagnosis, and to assess the factors associated with late diagnosis, early mortality, and ART initiation in China between 2006 and 2014.

Methods

Data sources and definitions

In China, all newly diagnosed HIV/AIDS cases and all recipients of free ART are registered into the Chinese Comprehensive Response Information Management System of HIV/AIDS (CRIMS). CRIMS is managed by the National Centre for AIDS/STD Control and Prevention (NCAIDS) of the Chinese Centre for Disease Control and Prevention (China CDC) and includes the National Case Reporting Database (NCRD) and the National Free Antiretroviral Therapy Database (NFATD). The NCRD collects data on newly diagnosed HIV/AIDS cases, including demographic characteristics, route of infection, site of HIV diagnosis or blood sample source, date of diagnosis, laboratory test results with corresponding test date, and date of death. These cases are followed up every 6 months. During each follow-up, CD4 cell count, counseling and behavior intervention, and other referral services are performed. The NCRD also collects additional data during each follow-up visit, including changes in demographic information, disease stage, CD4 cell count, information on behavioral determinants, and details of ART. The NFATD includes all cases that meet the national treatment criteria and have received free treatment. In China, the national criteria for treatment is a CD4 cell count of less than 350 cells/mm3 (as of 2009) and later, of less than 500 cells/mm3 (as of 2014), or being reported as having AIDS, or having WHO stage 3 or 4 HIV/AIDS and having been referred for ART [2629]. Information on the individual’s drug regiment during each follow-up visit is recorded and then uploaded to the CRIMS.
A detailed description of the NCRD and NFATD has been published elsewhere [26], including a discussion of quality control of lab work [28]. There have been several important ART studies based on the data from these two systems in recent years [2729]. In this study, we updated the results in continuation with earlier findings from the cohort study [27]. We included all newly diagnosed HIV/AIDS cases between 1 January 2006 and 31 December 2014 in mainland China involving individuals aged 15 years and over and excluded individuals who could not be located by local CDCs during follow-up visits.
There were several explanations for the term “late diagnosis” [3032]. In this study, we classified a case as a “late diagnosis” if an individual was reported as 1) having been diagnosed with AIDS or 2) having been diagnosed with WHO stage 3 or 4 HIV/AIDS, or 3) having an initial CD4 cell count of less than 200/mm3 within one year after the date of HIV diagnosis. Early mortality was defined as death from AIDS-related causes within one year of an HIV/AIDS diagnosis. Cases without a death certificate or without being lost to follow-up as of 31 December 2014, were assumed to be alive. Cases who died of overdose drug use or suicide were excluded.
We defined preventable early mortality as the estimated number of AIDS-related deaths within one year of diagnosis attributed to late diagnosis. The number of preventable early mortality equals to the number of observed AIDS-related deaths within one year of diagnosis minus the estimated number of AIDS-related deaths within one year of diagnosis according to the early mortality rate of those who received timely HIV diagnoses.

Statistical analysis

We used SAS software (version 9.4; SAS Institute; Cary, NC) for data analysis and MapInfo Professional software (version 15.0; Pitney Bowes; USA) for maps creation. Descriptive analysis was done for late diagnoses across all cases, including gender, age at HIV diagnosis, marital status, education level, route of transmission, ethnic group, and screening sites. Screening sites were categorized into three groups: VCT sites, hospitals, and detention centers. Transmission routes were classified into five groups: heterosexual, homosexual, injection drug use, sexual contact and injection drug use, and former paid blood/plasma donation. Odds ratio (OR) was used to assess the factors associated with late diagnosis by means of univariate and multivariate logistic regression models. Variables for which P values were less than 0.05 were considered to be statistically significant.

Results

A total of 563,961 individuals were newly diagnosed with HIV infection in mainland China during the period between 1 January 2006 and 31 December 2014. A total of 35,727 subjects were excluded from this analysis, as 28,544 cases could not be traced after the initial positive tests and 7183 cases concerned individuals were under 15 years of age (Fig. 1). Among the remaining 528,234 individuals, the majority were male (72.7%), married (50.2%), had attained a middle school level education or higher (60.8%), heterosexual (63.2%), and belonged to the Han ethnic group (74.6%). Most were diagnosed a t hospitals (44.7%) and VCT sites (28.4%) (Table 1).
Table 1
Demographic Characteristics and factors associated with late diagnosis in China between 2006 and 2014 (N = 528,234)
Categories
Newly diagnosed (age > 14 years old)
n (%) of Late diagnosis
Unadjusted OR (95%CI)
Adjusted OR (95%CI)
Total
528,234
179,700(34.0)
_
_
Year of HIV diagnosis
 2006
26,027
8823(33.9)
Ref.
Ref.
 2007
32,538
11,427(35.1)
1.06(1.02–1.09)
1.04(1.00–1.08)
 2008
40,690
13,734(33.8)
0.99(0.96–1.03)
0.93(0.89–0.96)
 2009
48,163
17,073(35.4)
1.07(1.04–1.11)
0.99(0.95–1.02)
 2010
53,375
19,700(36.9)
1.14(1.11–1.18)
0.99(0.96–1.03)
 2011
67,256
23,944(35.6)
1.08(1.05–1.11)
0.89(0.86–0.92)
 2012
76,716
26,598(34.7)
1.04(1.01–1.07)
0.84(0.81–0.87)
 2013
85,518
29,291(34.3)
1.02(0.99–1.05)
0.82(0.79–0.85)
 2014
97,951
29,110(29.7)
0.83(0.80–0.85)
0.65(0.63–0.68)
Sex
 Female
144,013
49,803(34.6)
Ref.
Ref.
 Male
384,221
129,897(33.8)
0.97(0.95–0.98)
1.15(1.13–1.17)
Age groups(years)
 15–24
74,796
12,174(16.3)
Ref.
Ref.
 25–34
163,089
44,161(27.1)
1.91(1.87–1.95)
187(1.82–1.91)
 35–44
132,507
51,750(39.1)
3.30(3.22–3.37)
2.78(2.72–2.85)
 45–54
70,158
32,262(46.0)
4.38(4.27–4.49)
3.25(3.17–3.34)
 55+
87,684
39,353(44.9)
4.19(4.09–4.29)
2.94(2.86–3.02)
Marital status
 Single, divorced, or widowed
256,895
74,319(28.9)
Ref.
Ref.
 Married or lives with partner
264,977
104,087(39.3)
1.59(1.57–1.61)
1.12(1.11–1.13)
Education
 Middle school or more
331,210
111,091(33.5)
Ref.
Ref.
 Primary school or less
191,811
67,212(35.0)
1.07(1.06–1.08)
0.87(0.86–0.89)
Occupation
 Other
278,138
84,141(30.3)
Ref.
Ref.
 Farmer or rural laborer
250,096
95,559(38.2)
1.43(1.41–1.44)
1.13(1.11–1.14)
Ethnic group
 Other
134,406
35,356(26.3)
Ref.
Ref.
 Han
393,828
144,344(36.7)
1.62(1.60–1.64)
1.30(1.28–1.32)
Route of HIV infection
 Heterosexual
333,753
126,658(37.9)
Ref.
Ref.
 Homosexual
85,252
20,891(24.5)
0.53(0.52–0.54)
0.71(0.70–0.73)
 Injection drug use
73,834
14,111(19.1)
0.39(0.38–0.39)
0.63(0.61–0.64)
 Sexual contact and injection drug use
5257
1147(21.8)
0.46(0.43–0.49)
0.71(0.66–0.76)
 Blood or plasma transfusion
16,767
12,910(77.0)
5.47(5.28–5.68)
4.18(4.02–4.35)
Sites of diagnosis
 VCT centers
150,157
54,260(36.1)
Ref.
Ref.
 Hospitals
236,047
97,220(41.2)
1.24(1.22–1.25)
1.17(1.15–1.19)
 Detention centers
43,231
5087(11.8)
0.24(0.23–0.24)
0.35(0.34–0.37)
others
98,799
23,133(23.4)
0.54(0.53–0.55)
0.59(0.58–0.61)
Migrant populationa
 No
402,155
143,160(35.6)
Ref.
Ref.
 Yes
126,079
36,540(29.0)
0.74(0.73–0.75)
0.94(0.93–0.96)
aMigrant population: people migrated from one county to another county and stay there for at least six months
In this cohort, 179,700 (34.0%) individuals newly diagnosed with HIV infection were classified as “late diagnosis” cases in accordance with the definition. The late diagnosis rate decreased from 33.9% in 2006 to 29.7% in 2014 (P < 0.01) (Fig. 2). The proportion of cases of late diagnosis were more than 55 % among four provinces in 2006, three provinces in 2010 and none in 2014 (Fig. 3).
The proportion of cases of late diagnosis was greater among those who were over 45 years old, married, farmers or rural laborers, and of Han ethnicity, infected through heterosexual transmission or former blood/plasma transfusion, diagnosed at hospitals, (Table 1). In addition, our results indicated that cases of late diagnosis increased with an increase in age in all calendar years during the study period.
As per our results, factors independently associated with an increased likelihood of late diagnosis were being male (aOR: 1.15, 95% CI: 1.13–1.17), being in an older age group (aOR: 3.25, 95% CI: 3.17–3.34 for 45–54 years old; aOR: 2.94, 95% CI: 2.86–3.02 for 55+ years old), having acquired HIV infection through former blood or plasma transfusion (aOR: 4.18, 95% CI: 4.02–4.35), being of Han ethnicity (aOR: 1.30, 95% CI: 1.28–1.32), being married or living with a partner (aOR: 1.15, 95% CI: 1.13–1.17), being farmers (aOR: 1.13, 95% CI: 1.11–1.14), and being tested at hospitals (aOR: 1.17, 95% CI: 1.15–1.19).
Around 52.0% of newly diagnosed cases (274,552) had their CD4 cell count results available within one month of HIV diagnosis (Table 2). This proportion increased from 19.0% in 2006 to 65.8% in 2014. Furthermore, this proportion was the lowest (29.7%) among those who were infected through injection drug use. Those who were diagnosed at VCT clinics received a timely (within one month) CD4 cell count testing of 60.9%.
Table 2
Initial CD4 cell counts after diagnosed of HIV newly diagnosed individuals in China between 2006 and 2014 (N = 528,234)
Characteristic
Newly diagnosed (age > 14 years old)
Initial CD4 cell count within one month
Initial CD4 cell count within one year
Initial CD4 cell counts < 200 cell/ul within one year
n
%
n
%
n
%
Year of HIV diagnosis
 2006
26,027
4950
19.0
9129
35.1
3901
42.7
 2007
32,538
8856
27.2
15,621
48.0
6282
40.2
 2008
40,690
14,475
35.6
23,979
58.9
8491
35.4
 2009
48,163
20,327
42.2
32,083
66.6
11,321
35.3
 2010
53,375
25,110
47.0
40,073
75.1
13,511
33.7
 2011
67,256
35,950
53.5
54,378
80.9
18,002
33.1
 2012
76,716
45,550
59.4
66,064
86.1
20,444
30.9
 2013
85,518
54,931
64.2
76,191
89.1
23,474
30.8
 2014
97,951
64,403
65.8
86,482
88.3
25,669
29.7
Route of HIV infection
 Heterosexual
333,753
183,602
55.0
264,332
79.2
96,527
36.5
 Homosexual
85,252
57,299
67.2
78,895
92.5
15,515
19.7
 Injection drug use
73,834
21,958
29.7
40,713
55.1
9168
22.5
 Sexual contact and injection drug use
5257
1760
33.5
3257
62.0
777
23.9
 Blood or plasma transfusion
16,767
7006
41.8
11,833
70.6
7142
60.4
Sites of diagnosis
 VCT centers
150,157
91,425
60.9
124,603
83.0
39,141
31.4
 Hospitals
236,047
118,702
50.3
176,834
74.9
73,114
41.3
 Detention centers
43,231
12,397
28.7
23,395
54.1
3196
13.7
 others
98,799
52,028
52.7
79,168
80.1
15,644
19.8
 Total
528,234
274,552
52.0
404,000
76.5
131,095
32.4
Our results indicate that 76.5% (404,000) of newly HIV diagnosed individuals received testing for CD4 cell count within one year of HIV diagnosis (Table 2). Of these individuals, 32.4% (131,095) had a CD4 cell count less than 200 cells/mm3. The proportion with a CD4 cell count test administered within one year increased during the study period from 35.1% in 2006 to 88.3% in 2014, and the proportion of CD4 cell count less than 200 cells/mm3 decreased from 42.7% in 2006 to 29.7% in 2014. Those infected through former blood or plasma transfusion witnessed a high proportion of CD4 cell count less than 200 cells/mm3. The proportion of CD4 cell count less than 200 cells/mm3 increased with age, from 13.3% in 15–24 age group to 44.8% in 55+ age group.

Early mortality and access to ART

Of the 179,700 individuals who received late diagnoses, excluding 1404 individuals who died of overdose drug use or suicide, the proportions receiving ART within one month of diagnosis and within one year of diagnosis were 30.1 and 65.4%, respectively. The percentage of the individuals who received late diagnoses, received ART, and died within one month of diagnosis was 0.51%. The percentage of the individuals who received late diagnoses, received ART, and died within one year of diagnosis was 7.4% (Table 3). 17.4% of individuals who received late diagnoses but did not receive ART died within one month of diagnosis, and 46.1% of those who received late diagnoses without ART died within one year of diagnosis. Upon further analysis, the early mortality was 20.8% (37,099/178,296) among those who received late diagnoses and 9.6% (32,626/341,072) among those with timely diagnoses (P < 0.01).
Table 3
Early mortality among late diagnosed individuals with or without ART, by month (N = 178,296)
Duration of time from diagnosis
Initial CD4 counts
ON ART
NO ART
N
No. of deatha
% of death
Na
No. of deatha
% of death
One month
0–49
33,897
325
0.96
15,344
2449
15.96
50–99
19,220
63
0.33
7153
516
7.21
100–199
37,747
44
0.12
13,934
330
2.37
200–349
17,685
14
0.08
6718
81
1.21
350–499
5135
3
0.06
3301
32
0.97
500-
2041
0
0.00
1977
10
0.51
No CD4 test
848
142
16.75
13,296
7316
55.02
subtotal
116,573
591
0.51
61,723
10,734
17.39
Three months
0–49
33,897
1551
4.58
15,344
5705
37.18
50–99
19,220
390
2.03
7153
1399
19.56
100–199
37,747
283
0.75
13,934
1000
7.18
200–349
17,685
61
0.34
6718
201
2.99
350–499
5135
15
0.29
3301
77
2.33
500-
2041
3
0.15
1977
34
1.72
No CD4 test
848
398
46.93
13,296
9674
72.76
subtotal
116,573
2701
2.32
61,723
18,090
29.31
Six months
0–49
33,897
2950
8.70
15,344
7963
51.90
50–99
19,220
880
4.58
7153
2253
31.50
100–199
37,747
678
1.80
13,934
1684
12.09
200–349
17,685
147
0.83
6718
359
5.34
350–499
5135
39
0.76
3301
157
4.76
500-
2041
14
0.69
1977
70
3.54
No CD4 test
848
560
66.04
13,296
10,838
81.51
subtotal
116,573
5268
4.52
61,723
23,324
37.79
Twelve months
0–49
33,897
4521
13.34
15,344
9796
63.84
50–99
19,220
1520
7.91
7153
3100
43.34
100–199
37,747
1385
3.67
13,934
2654
19.05
200–349
17,685
361
2.04
6718
628
9.35
350–499
5135
107
2.08
3301
307
9.30
500-
2041
53
2.60
1977
141
7.13
No CD4 test
848
690
81.37
13,296
11,836
89.02
subtotal
116,573
8637
7.41
61,723
28,462
46.11
aThose who died of overdose drug use or suicide were excluded
Among PLHIV who received late diagnoses, the proportion experiencing early mortality declined annually from 2006 to 2014 with an increase in the proportion receiving ART (Table 4). The early mortality rates for individuals who received late diagnoses were 29.5% in 2006 and 14.5% in 2014. At the same time, the treatment coverage rates for these individuals within one year of diagnosis were 39.5% in 2006 and 73.9% in 2014. The treatment coverage rate for those who reported having had sex with men was highest (82.8%) (p < 0.01), therefore, this group also experienced the lowest rate of early mortality (8.0%) (Table 4).
Table 4
Access to ART and early mortality among late diagnosis individuals within one year of diagnosis between 2006 and 2014 (N=178,296)
Characteristics
Late diagnosis (age>14 years old)*
N (% of access to ART within one month)
N (% of access to ART within one year)
N (% of died after receiving ART)
χ2
P-value b
Year of HIV diagnosis
    
141.52
<0.01
 2006
8675
1436(16.6)
3429(39.5)
267(7.8)
  
 2007
11252
2105(18.7)
5126(45.6)
341(6.7)
  
 2008
13535
3051(22.5)
7387(54.6)
568(7.7)
  
 2009
16874
3906(23.1)
9527(56.5)
621(6.5)
  
 2010
19532
4498(23.0)
12021(61.5)
679(5.6)
  
 2011
23741
6383(26.9)
16355(68.9)
1076(6.6)
  
 2012
26445
8524(32.2)
19038(72.0)
1495(7.9)
  
 2013
29192
11068(37.9)
22212(76.1)
1897(8.5)
  
 2014
29050
12668(43.6)
21478(73.9)
1693(7.9)
  
Sex
    
137.54
<0.01
 Female
49561
15132(30.5)
32806(66.2)
1959(6.0)
  
 Male
128735
38507(29.9)
83767(65.1)
6678(8.0)
  
Age group (years)
    
871.48
<0.01
 15-24
12082
3107(25.7)
8305(68.7)
317(3.8)
  
 25-34
43688
12146(27.8)
28734(65.8)
1436(5.0)
  
 35-44
51244
15499(30.2)
33684(65.7)
2430(7.2)
  
 45-54
32084
10846(33.8)
21947(68.4)
1832(8.3)
  
 55+
39198
12041(30.7)
23903(61.0)
2622(11.0)
  
Marital status
    
11.08
<0.01
 Single, divorced, or widowed
73626
20957(28.5)
48061(65.3)
3411(7.1)
  
 Married or lives with partner
103411
32483(31.4)
67970(65.7)
5177(7.6)
  
Education
    
488.54
<0.01
 Middle school or more
110338
34898(31.6)
77177(69.9)
4792(6.2)
  
 Primary school or less
66599
18585(27.9)
39012(58.6)
3826(9.8)
  
Occupation
    
663.26
<0.01
 Other
83510
25305(30.3)
57787(69.2)
3130(5.4)
  
 Farmer or rural laborer
94786
28334(29.9)
58786(62.0)
5507(9.4)
  
Ethnic group
    
16.57
<0.01
 Others
34969
9013(25.8)
19866(56.8)
1335(6.7)
  
 Han
143327
44626(31.1)
96707(67.5)
7302(7.6)
  
Route of HIV infection
    
622.49
<0.01
 Heterosexual
126054
40124(31.8)
83978(66.6)
6547(7.8)
  
 Homosexual
20832
6951(33.4)
17167(82.4)
646(3.8)
  
 Injection drug use
13531
1955(14.4)
5809(42.9)
372(6.4)
  
 Sexual contact and IDU
1102
245(22.2)
560(50.8)
31(5.5)
  
 Blood or plasma transfusion
12841
3722(29.0)
7457(58.1)
917(12.3)
  
Sites of diagnosis
    
681.88
<0.01
 VCT centers
53825
17809(33.1)
36452(67.7)
2346(6.4)
  
 Hospitals
96608
29659(30.7)
62791(65.0)
5683(9.1)
  
 Detention centers
4859
197(4.1)
1563(32.2)
62(4.0)
  
 others
23004
5974(26.0)
15767(68.5)
546(3.5)
  
Migrant population a
    
10.03
<0.01
 No
142108
43658(30.7)
93717(65.9)
7056(7.5)
  
 Yes
36188
9981(27.6)
22856(63.2)
1581(6.9)
  
Initial CD4+ cell count
    
10298.66
<0.01
 0-49
49241
18191(36.9)
33897(68.8)
4521(13.3)
  
 50-99
26373
9778(37.1)
19220(72.9)
1520(7.9)
  
 100-199
51681
17268(33.4)
37747(73.0)
1385(3.7)
  
 200-349
24403
6167(25.3)
17685(72.5)
361(2.0)
  
 350-499
8436
1177(14.0)
5135(60.9)
107(2.1)
  
 500-
4018
476(11.8)
2041(50.8)
53(2.6)
  
 No CD4 records
14144
582(4.1)
848(6.0)
690(81.4)
  
Total
178296
53639(30.1))
116573(65.4)
8637(7.4)
  
aThose who died of overdose drug use or suicide were excluded
bThe proportion of those who died after ART within one year is compared by different characteristics

Estimation of preventable early mortality

Early mortality among those who received timely HIV diagnoses was 9.6%. Basing our assumptions of previous research [3032], we presumed in our study that 1) early mortality would be reduced to 9.6% if there were no late diagnoses; 2) there would be no effect on deaths occurring more than a year after diagnosis; and 3) there would no other competing risks. Based on these conjectures, only 17,116 deaths would have been expected from 2006 to 2014 within a year of diagnosis if the diagnosis was timely. That is, 19,983 deaths would have been avoided during this period, compared to the 37,099 deaths actually observed among the group with late HIV diagnoses. Therefore, the current burden of early mortality would be reduced by about 53.9%.

Discussion

It has been thirty years since HIV testing first became available [33]. Despite the decades of availability of testing, it was estimated that at least one-fourth of PLHIV worldwide were unaware of their infection [24, 3439], and that this ratio could be even higher in China [24].Our results indicate that promoting timely diagnosis and treatment provided a survival advantage to PLHIV, and that almost 54% of deaths that occurred within one year of HIV diagnosis could thus be prevented. Our study expanded upon the existing literature [16, 32, 37, 40, 41] by evaluating late diagnoses among all HIV cases identified between 2006 and 2014 in China, by assessing and mapping the trend of late diagnosis over time and by evaluating factors associated with late diagnosis among HIV cases in China.
In our study, 34.0% of HIV cases were considered to have received late diagnoses between 2006 and 2014. The late diagnosis rate fluctuated from 2006 to 2014, but slightly decreased from 36.9% in 2010 to 29.7% in 2014 (P < 0.01). This declining could be due to the implementation of the provider-initiated HIV testing and counseling (PITC) strategy since 2009. After the initiating of PITC, the HIV testing was significantly scaled up in most of provinces in China [37, 38, 42]. The scaling up of HIV self-testing in China could be another reason for this phenomenon. For example, around 30% of MSM in China self-reported that they ever self-tested in 2016 [36].
The propensity to receive late HIV testing was greater for older people, those who had acquired HIV infection through former blood or plasma transfusion or heterosexual behaviors, individuals of Han ethnicity, married individuals, and farmers. These results are consistent with the findings of previous studies [31, 43], with the exception of some studies in the U.S. indicated that younger people was more likely to receive late testing [44, 45]. In recent years, spouses’ and regular partners’ testing was scaled up in China, because of a series of national and provincial laws, regulations, and policy initiatives.
The majority of late diagnoses occurred among those who were infected with HIV through heterosexual behaviors. It indicated that there might have been a prolonged period of transmission risk to their sexual partners. Strategies, promoting rapid HIV testing at primary level of health institutions, promoting HIV self-testing, and increasing collaboration with community based organizations (CBOs), should be further implemented. Also, the risk of late diagnosis was significantly higher for those who were infected through former blood or plasma transfusion. Illegal paid plasma donation was prominent in central China in the 1990s and resulted in the infection of the majority of donors with the HIV virus [26, 46, 47]. Most of these PLHIV did not seek testing due to societal discrimination and stigma against HIV. As a result, they were diagnosed with HIV only after they experienced symptoms. Most of these people are located in four provinces in central China, as shown in Fig. 3.
However, the proportion of late testing has decreased among men who have sex with men (MSM) and injection drug users in recent years. This finding may have been due to ongoing intervention programs that promoted testing in these high risk groups [48, 49], such as methadone maintenance treatment (MMT) for injection drug users and free HIV testing for MSM provided by CBOs and VCT clinics. Similar results have been found in other studies [45].
Individuals who present at an advanced stage of immunosuppression are at high risk of clinical events and death and are more likely to have a poor response when they start ART [50, 51]. The proportion of people receiving late diagnoses among newly diagnosed individuals remained at more than 30% between 2006 and 2013. However, this proportion has been in decline since 2010. In an era where effective and free testing and free treatment options are available in China, it is alarming that there is a substantial proportion of people were late diagnosed, and they are at higher risk of early death. A records-based retrospective cohort study in China found that the highest mortality rates for AIDS-related death and all-cause death were found in the first year of follow up after HIV diagnosis [52]. This phenomenon could be explained by the fact that about half of the participating cases had already progressed to AIDS before being identified, progression to AIDS was one of the strongest risk factors for AIDS-related death, with an aHR of 7.42 [52].
Individuals who present at an advanced stage of immunosuppression are at high risk of AIDS related diseases and death as well as more likely to have a poorer response to ART [36, 53]. Both HIV testing and ART have been free for PLHIV in China since 2003 [54]. In spite of this policy, our results indicate that as many as 30% of all newly diagnosed individuals received late diagnoses. Shortening the time from infection to measurement of CD4 cell counts could be an important window for early treatment. We infer that the time from infection to CD4 measurement is a useful indicator for monitoring delays in access to HIV medical care among newly diagnosed PLHIV [55]. In our analysis, 52.0% of newly diagnosed individuals had their CD4 cell counts available within one month of HIV diagnosis. This proportion increased from 19.0% in 2006 to 65.8% in 2014. It is very important for late diagnosed individuals to receive CD4 cell count testing immediately, so that they can receive referrals for timely ART and thus reduce their risk of death. In our study, this proportion of cases received ART within one month after the diagnoses increased from 16.6% in 2006 to 43.6% in 2014. The average proportion of having CD4 counts within one year was 76% from 2006 to 2014. The causes of not having CD4 counts testing within one year included death before having CD4 counts, lost to follow up, and inconvenience to access to CD4 count test. To shorten the time to CD4 cell count testing and to improve access to regular testing and treatment, efforts were taken in the past few years to dramatically improve referrals and integration of patient tracking between the health facilities responsible for patients follow up, CD4 cell count testing, and ART delivery [56].
Our analysis suggests that groups at high risk of late diagnosis should be targeted for appropriate public health intervention and encouraged to seek earlier treatment. Scaling up HIV testing is one of the important strategies in implementing this goal. This strategy may bring out a greater proportion of hidden individuals infected with HIV [57]. Another strategy would be to consider population-wide screening for HIV, such as for patients in hospitals. In the U.S., the CDC recommends routine HIV counseling and testing in healthcare settings for patients aged 13–64 years, unless the local HIV prevalence is known to be less than 0.1% [1].
There are some limitations to consider while interpreting our findings. Firstly, 2.3% (12,352/528234) individuals were lost to follow-up after HIV diagnoses, and then CD4 cell counts data or having WHO stage 3 or 4 of them were not available at diagnosis. Thus, it is possible that some individuals with AIDS may have been misclassified as having HIV. However, the resulting misclassification will be non-differential and might bias the estimates towards the null, because the proportion of individuals misclassified does not depend on the individual with respect to other variables on the analysis [58]. Secondly, our results couldn’t assess differences in mortality in late diagnosed individuals who access to ART based on ART regimen. It needs further research.

Conclusion

Even with these limitations, our results still indicate that it is important to increase the accessibility of HIV testing services. Routine testing for most individuals has been recommended as a cost-effective strategy and efforts to promote such testing should be developed [40, 53].

Acknowledgements

The authors thank all of the health care and laboratory staff at all levels who participated in HIV/AIDS diagnoses, follow-up and data collection for this study.

Funding

This study was funded from the National Health and Family Planning Commission of the People’s Republic of China (grant#131–11–0001-0501). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
This study was a secondary data analysis using existing Chinese government HIV/AIDS CRIMS data. Therefore, no additional study specific informed consent was necessary for this current study. Patient records and information were de-identified prior to analysis. This study protocol was reviewed and approved by the Institutional Review Board of the National Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and Prevention (approval #X160310409).

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
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Metadaten
Titel
“Late for testing, early for antiretroviral therapy, less likely to die”: results from a large HIV cohort study in China, 2006–2014
verfasst von
Houlin Tang
Yurong Mao
Weiming Tang
Jing Han
Juan Xu
Jian Li
Publikationsdatum
01.12.2018
Verlag
BioMed Central
Erschienen in
BMC Infectious Diseases / Ausgabe 1/2018
Elektronische ISSN: 1471-2334
DOI
https://doi.org/10.1186/s12879-018-3158-x

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