3 by 5, Millenium Development Goals (MDG), US President's Emergency Plan for AIDS Relief (PEPFAR), N/A, Universal Access (UA), Additional Recommended Indicators, 2009 UN General Assembly Special Session on HIV/AIDS (UNGASS)

Number of cases of sexually transmitted infections treated

Number of cases of sexually transmitted infections treated

The following sexually transmitted infections have been shown to be important co-factors for HIV
transmission or acquisition and should therefore be considered for the assessment: curable genital
ulcers, notably chancroid and syphilis; other curable sexually transmitted infections including Neisseria
gonorrhoeae and Chlamydia trachomatis, which may present as urethral discharge. Where treatment of
herpes viral infection is included as a part of national guidelines, assessment for appropriate genital ulcer

ID: 
761
What it measures: 

Similar types of behavior put people at risk for both sexually transmitted infections and HIV. People
with sexually transmitted infections may be at higher risk of acquiring or transmitting HIV infection
due to the co-factor effect of an existing sexually transmitted infection. Services for sexually transmitted
infections provide opportunities for comprehensive care that includes early treatment; counseling and
communication about behavior change and information for sexual partners; access to testing for HIV
infection; and an entry point into care programs for people living with HIV. Treating sexually transmitted
infections quickly and effectively reduces the possibility of further transmission of infection.

Numerator: 

Number of cases of sexually transmitted infections (determined syndromically or
etiologically) identified at selected facilities that were treated

Data Type: 
Count
Unit: 
N/A
Multiplier: 
N/A
Composite Indicator: 
No
Calculation: 
Not applicable
Method of measurement: 
Tools: program records Frequency: quarterly Disaggregation: By sex (male, female) and age To assess whether sexually transmitted infections have been treated according to national guidelines, a health facility survey should be performed. In this case, the indicator would be defined as follows. Numerator: Number of cases of sexually transmitted infections treated according to national guidelines Denominator: Total number of cases of sexually transmitted infections at selected facilities health facility surveys in a selection of facilities Frequency: every two to three years
Data Collection
Data Collection Method: 
Programme records
Indicator Type: 
Programme / Service Delivery
Indicator Level: 
National
Disaggregations
Education: 
N/A
Gender: 
Female
Male
Geographic Location: 
N/A
Pregnancy: 
N/A
Sector: 
N/A
Target: 
N/A
Time Period: 
N/A
Type of Orphan: 
N/A
Vulnerability Status: 
N/A
HIV Status: 
N/A
Service Type: 
N/A
Type/Timing of Testing: 
N/A
Condom Type: 
N/A
Preferred Indicator: 
TBD
Agency: 
Global Fund to Fight AIDS, Tuberculosis and Malaria (GFATM)
Relevance: 
N/A
Status: 
Retired
Keywords
Programme Focus General: 
Treatment
Programme Focus Specific: 
Sexually-Transmitted Infections (STI)
Target Population: 
Age: Not Specified
Sex: All
Goal - Initiative or Country: 
N/A

Number of circumcised clients experiencing at least one moderate or severe adverse event (AE) during or following surgery, within the reporting period

Number of circumcised clients experiencing at least one moderate or severe adverse event (AE) during or following surgery, within the reporting period

ID: 
758
What it measures: 

3 randomized controlled clinical trials in sub-Saharan Africa demonstrated a 60% reduction in risk of female-to-male HIV transmission among men randomized to receive circumcision (compared to uncircumcised controls). This evidence is supported by long-standing ecologic and observational data. Elective surgical male circumcision confers a partially protective effect against HIV acquisition for HIV-negative men at risk for acquiring HIV from HIV-infected female sexual partners, and may be particularly beneficial in generalized HIV epidemics and where HIV prevalence is high and male circumcision prevalence is low. Like all surgeries, male circumcision is not without risk, and the performance and reporting of safe MC services depends in part upon skill and quality of surgery, effectiveness of post-operative instructions, willingness or ability of the patient to follow post-operative instructions, suitability of the surgical candidate, level of CD4 count if HIV-positive, and the judgment of the healthcare personnel assessing AEs. Intra- and post-operative complications must be monitored to ensure maximization of the provision of safe, quality MC services, and in turn engender trust in communities and foster high demand for MC services.

Numerator: 

Number of clients circumcised that experience (reporting back to the respective circumcising program) one or more moderate or severe AE(s) during the reporting period, according to the date of MC surgery, and disaggregated by severity (moderate and/or severe), timing of AE(s), and specific AE(s)

Denominator: 

N/A

Data Type: 
Count
Unit: 
N/A
Calculation: 
N/A
Method of measurement: 
The numerator can be generated by summing the clients experiencing moderate and severe adverse events documented in Adverse Event Monitoring Logs or client medical records maintained by programs. Explanation: Clients who have documentation in the facility record that they experienced one or more moderate or severe AEs (AEs would necessarily have to be reported back to the respective circumcising program) during or following MC surgery meet the definition for the numerator. It is the date of surgery, not the date of AE(s) that must fall within the reporting period. For instance, if the reporting period is October 1, 2009, through December 31, 2009, and a client was circumcised December 29, 2009 and had a moderate adverse event on January 2, 2010, then this client would meet the definition and be included in the numerator (since his surgery was performed within the reporting period, even though his adverse event occurred after the reporting period). Adverse events must be documented in a client’s clinic record or registry by the facility that performed the surgery. For this reason, it is anticipated that the indicator reporting may reflect fewer adverse events than actually occurred (as clients experiencing AE(s) may not return to the facility at all, seek care for AE(s) elsewhere, or the facility may fail to document occurrence of the AE(s) in the appropriate record). For reporting purposes, AEs include MC cases involving an occupational exposure to blood/body fluids. Occupational exposure to blood/body fluids (splash, sharps injuries) are based upon guidelines set forth in the WHO/ILO Post-exposure Prophylaxis to Prevent HIV Infection (http://www.who.int/hiv/pub/guidelines/PEP/en/index.html) For the specific moderate/severe AEs listed in the disaggregation above, the following guidance for distinguishing between moderate and severe is offered. Routine reporting of moderate and severe AEs is all that is recommended. AEs of seriousness less than moderate should not be reported. ANESTHESIA REACTION: -Moderate: Reaction to anesthetic requiring medical treatment on site, but not transfer to another facility (Palpitations, vaso-vagal reactions, or emesis would not qualify as moderate AE(s) unless such reaction(s) were so serious as to require medical treatment). -Severe: Anaphylaxis or other reaction requiring hospitalization or referral/transfer to another facility BLEEDING: -Moderate: Intra-operative bleeding that requires a pressure dressing to control; or post-operative bleeding that requires a special return to the clinic for medical attention (Intra-operative bleeding that is easily controlled or post-operative spotting of the bandage with blood would not qualify as a moderate AE). -Severe: Intra-operative bleeding requiring blood transfusion, transfer to another facility, or hospitalization; or post-operative bleeding that requires surgical re-exploration, hospitalization, or transfer to another facility. INFECTION: -Moderate: Purulent discharge from the wound (Erythema around the incision line, by itself, would not be serious enough to qualify as a moderate AE) -Severe: Cellulitis or wound necrosis PAIN (INTRA- AND POST-OPERATIVE): -Moderate: Pain serious enough to result in disability (as evidenced by loss of work or cancellation of normal activities) that lasting for at least 4 days after surgery but not more than 7 days -Severe: Pain serious enough to result in disability (as evidenced by loss of work or cancellation of normal activities) lasting for at least 8 days after surgery. Pain that is so extraordinary as to result in early termination of surgery or administration of general anesthesia (where possible) would also be considered a severe pain AE. WOUND DISRUPTION: -Moderate: Surgical re-exploration is required, but hospitalization or referral to another facility is not necessary (Re-suturing, by itself, would not be considered serious enough to qualify as a moderate wound disruption AE) -Severe: Referral/transfer to another facility or hospitalization is required. SEXUAL DYSFUNCTION/UNDESIRABLE SENSORY CHANGES: -Moderate: Post-operative changes that impair or preclude sexual function for between 3 and 6 months after the date of surgery (sexual dysfunction for a shorter period would not qualify as a moderate AE) -Severe: Post-operative changes that impair or preclude sexual function for greater than 6 months after the date of surgery SCARRING/DISFIGUREMENT/POOR COSMETIC RESULT; EXCESS SKIN REMOVAL; INJURY TO GLANS: -Scarring/disfigurement/poor cosmetic result Moderate: Scarring/disfigurement is discernible but re-operation not required (absence of discernible scarring/disfigurement, despite a client’s complaint about the surgical outcome, would not be considered a moderate AE). -Excess skin removal Moderate: Tightening of the skin is discernible but re-operation not required (absence of discernible tightening of skin, despite a client’s complaint about the surgical outcome, would not be considered a moderate AE). -Injury to glans/shaft Moderate: Abrasion of the glans or shaft requiring pressure dressing or additional surgical intervention to stop bleeding -Scarring/disfigurement/poor cosmetic result Severe: Requires re-operation or referral/transfer to another facility -Excess skin removal Severe: Requires re-operation or referral/transfer to another facility -Injury to glans/shaft Severe: Severing of the glans or shaft OCCUPATIONAL EXPOSURE: -Moderate: All occupational exposures are moderate (none are mild or severe) OTHER: EXCESS SWELLING OF PENIS/SCROTUM (INCLUDING HEMATOMA); DIFFICULTY URINATING; OTHER: -Excess swelling of penis/scrotum (including hematoma) Moderate: Symptoms /signs so extraordinary as to cause disability (as evidenced by loss of work or cancellation of normal activities) lasting for at least 4 days after surgery but not more than 7 days. -Difficulty urinating Moderate: Partial obstruction requiring a special return to the clinic but no additional treatment (transient difficulty urinating that resolves on its own would not be considered a moderate AE). -Other Moderate: Other adverse events related to the surgery that result in disability (as evidenced by loss of work or cancellation of normal activities) lasting for at least 4 days after surgery but not more than 7 days. -Excess swelling of penis/scrotum (including hematoma) Severe: Surgical re-exploration required or symptoms /signs so extraordinary as to cause disability (as evidenced by loss of work or cancellation of normal activities) lasting for at least 8 days after surgery -Difficulty urinating Severe: Complete obstruction and/or requires referral for treatment or surgery to correct. -Other Severe: Other AE(s) related to the surgery that result in disability (as evidenced by loss of work or cancellation of normal activities) lasting for at least 8 days after surgery, or result in hospitalization or referral/transfer to another facility.
Data Collection
Data Collection Method: 
Patient record
Measurement Frequency: 
Continuously
Epidemic Type: 
Concentrated/low level
Generalized
Indicator Level: 
National
Disaggregations
Education: 
N/A
Gender: 
N/A
Geographic Location: 
N/A
Pregnancy: 
N/A
Sector: 
N/A
Target: 
N/A
Time Period: 
N/A
Type of Orphan: 
N/A
Vulnerability Status: 
N/A
HIV Status: 
N/A
Service Type: 
N/A
Type/Timing of Testing: 
N/A
Condom Type: 
N/A
Strengths and weaknesses: 

Programs are recommended to report the number clients experiencing moderate or severe adverse events to allow for monitoring of safe, quality service provision. Frequency and frequency of severity, of AEs above ‘an acceptable level’ is an indication of the need for investigation into causes and possible interventions. Further, disaggregation by timing of adverse event may inform planning of post-operative care considerations, particularly from mobile/remote services that may have limited availability following surgery. Disaggregation by specific type of AE may help determine the need for additional training to prevent or manage certain complications.

Preferred Indicator: 
TBD
Agency: 
The President's Emergency Plan for AIDS Relief (PEPFAR)
Relevance: 
US President's Emergency Plan for AIDS Relief (PEPFAR)
Status: 
Active
Keywords
Programme Focus General: 
Prevention
Target Population: 
Age: Not Specified
Sex: Men Only
Goal - Initiative or Country: 
Initiative

Reduction in Mother-to-child Transmission

Percentage of infants born to HIV-infected mothers who are infected

 

Alias: 
 UNAIDS/WHO (Infants and Children): HIV-infected infants born to HIV-infected mothers Global Fund: Reduced mother-to-child HIV transmission
ID: 
670
What it measures: 

 To assess progress towards eliminating mother-to-child HIV transmission.

In high-income countries, strategies such as antiretroviral therapy during pregnancy and following birth,
and the use of breastfeeding substitutes have greatly reduced the rate of mother-to-child HIV transmission. In low-income countries, signifi cant difficulties exist in implementing these strategies due to constraints in accessing, affording and using voluntary counselling and testing services, reproductive health, and maternal and child health services, which have integrated prevention of mother-to-child transmission interventions, including breast milk substitute (where this is part of the country’s policy on prevention of mother-tochild transmission). Nevertheless, substantial reductions in mother-to-child transmission can be achieved through approaches such as short-course antiretroviral prophylaxis.
 

Numerator: 

Not applicable

Denominator: 

Not applicable

Data Type: 
Percent
Unit: 
N/A
Multiplier: 
N/A
Composite Indicator: 
No
Calculation: 
The indicator will be calculated by taking the weighted average of the probabilities of mother-to-child transmission for pregnant women receiving and not receiving HIV prophylaxis, the weights being the proportions of women receiving and not receiving various prophylactic regimes.
Method of measurement: 
Spectrum, or other statistical modelling that uses programme coverage and efficacy studies The indicator will be calculated by taking the weighted average of the probabilities of mother-to-child transmission for pregnant women receiving and not receiving HIV prophylaxis, the weights being the proportions of women receiving and not receiving various prophylactic regimes.  
Data Collection
Data Collection Method: 
Programme records
Estimate
Measurement Frequency: 
Annual
Epidemic Type: 
Concentrated/low level
Generalized
Indicator Type: 
Disease Impact
Indicator Level: 
National
Disaggregations
Education: 
N/A
Gender: 
N/A
Geographic Location: 
N/A
Pregnancy: 
N/A
Sector: 
N/A
Target: 
N/A
Time Period: 
N/A
Type of Orphan: 
N/A
Vulnerability Status: 
N/A
HIV Status: 
N/A
Service Type: 
N/A
Condom Type: 
N/A
Strengths and weaknesses: 

 This indicator focuses on prevention of mother-to-child transmission of HIV through increased provision
of antiretroviral medicines. The Spectrum HIV estimation modelling software takes into consideration the
type of antiretroviral regimen as well as additional factors that influence HIV transmission rates such as
infant feeding practices. For further information on Spectrum please consult the webpage of the UNAIDS/
WHO Estimates and Projections Reference Group listed below.
 

Preferred Indicator: 
Core National Indicator - UNGASS
Agency: 
Joint United Nations Programme on HIV/AIDS (UNAIDS)
The President's Emergency Plan for AIDS Relief (PEPFAR)
World Health Organisation (WHO)
Relevance: 
2009 UN General Assembly Special Session on HIV/AIDS (UNGASS)
Universal Access (UA)
US President's Emergency Plan for AIDS Relief (PEPFAR)
Status: 
Active
Keywords
Programme Focus General: 
Prevention
Programme Focus Specific: 
Prevention of Mother-to-Child Transmission (PMTCT)
HIV Prevalence
Target Population: 
Age: Infants
Sex: All
Goal - Initiative or Country: 
Initiative

HIV Treatment: Survival After 12 Months on Antiretroviral Therapy

Percentage of adults and children with HIV known to be on treatment 12 months after initiation of antiretroviral therapy

Alias: 
WHO (ARV): Survival at 6, 12, 24, 36, etc. months after initiation of treatment WHO (3 by 5): Survival
ID: 
669
What it measures: 

To assess progress in increasing survival among infected adults and children by maintaining them on antiretroviral therapy.

One of the goals of any antiretroviral therapy programme is to increase survival among infected individuals. As provision of antiretroviral therapy is scaled up in countries around the world, it is also important to understand why and how many people drop out of treatment programmes. These data can be used to demonstrate the effectiveness of those programmes and highlight obstacles to expanding and improving them.
 
 

Numerator: 

Number of adults and children who are still alive and on antiretroviral therapy at 12 months after initiating treatment

Explanation of the numerator:

The numerator requires that adult and child patients must be alive and on antiretroviral therapy at 12 months after their initiation of treatment. For a comprehensive understanding of survival, the following data must be collected:
http://www.unaids.org/en/HIV_data/Methodology/default.asp Number of adults and children in the antiretroviral therapy start-up groups initiating therapy at least 12 months prior to the end of the
reporting period;
• Number of adults and children still alive and on antiretroviral therapy at 12 months after initiating treatment.
The numerator does not require patients to have been on antiretroviral therapy continuously for the 12-month period. Patients who may have missed one or two appointments or drug pick-ups, and temporarily stopped treatment during the 12 months since initiating treatment but are recorded as still being on treatment at month 12 are included in the numerator. On the contrary, those patients who have died, stopped treatment or been lost to follow-up at 12 months since starting treatment are not included in the numerator.

For example, for those patients who started antiretroviral therapy in May 2005, if at any point during the period May 2005 to May 2006 these patients die, are lost to follow-up (and do not return), or stop
treatment (and do not restart), then at month 12 (May 2006), they are not on antiretroviral therapy, and not included in the numerator. Conversely, a patient who started antiretroviral therapy in May 2005
and who missed an appointment in June 2005, but is recorded as on antiretroviral therapy in May 2006 (at month 12) is on antiretroviral therapy and will be included in the numerator. What is important is
that the patient who has started antiretroviral therapy in May 2005 is recorded as being alive and on therapy after 12 months, regardless of what happens from May 2005 to May 2006.

Denominator: 

Total number of adults and children who initiated antiretroviral therapy who were expected to achieve 12-month outcomes within the reporting period, including those who have died since starting
therapy, those who have stopped therapy, and those recorded as lost to follow-up at month 12.

Explanation of denominator:

The denominator is the total number of adults and children in the antiretroviral therapy start-up groups who initiated therapy at any point during the 12 months prior to the beginning of the reporting period,
regardless of their 12-month outcome. For example, for the reporting period 1 January to 31 December 2007, this will include all patients who started antiretroviral therapy during the 12-month period from
1 January to 31 December 2006. This includes all patients, both those on antiretroviral therapy as well as those who are dead, have stopped treatment or are lost to follow-up at month 12.

At the facility level, the number of adults and children on antiretroviral therapy at 12 months includes patients who have transferred in at any point from initiation of treatment to the end of the 12-month period
and excludes patients who have transferred out during this same period to refl ect the net current cohort at each facility. In other words, at the facility level, patients who have transferred out will not be counted
either in the numerator or the denominator. Similarly, patients who have transferred in will be counted in both the numerator and denominator.

At the national level, the number of transferred-in patients should match the number of transferred-out patients. Therefore, the net current cohort (the patients whose outcomes the facility is currently
responsible for recording—the number of patients in the start-up group plus any transfers in, minus any transfers out) at 12 months should equal the number in the start-up cohort group 12 months prior.

Data Type: 
Percent
Unit: 
N/A
Multiplier: 
N/A
Composite Indicator: 
No
Calculation: 
Numerator / Denominator
Method of measurement: 
Antiretroviral therapy registers and antiretroviral therapy cohort analysis report form The reporting period is defined as any continuous 12-month period that has ended within a pre-defined number of months from the submission of the report. The pre-defined number of months can be determined by national reporting requirements. If the reporting period is 1 January to 31 December 2009, countries will calculate this indicator by using all patients who started antiretroviral therapy any time during the 12-month period from 1 January to 31 December 2008. If the reporting period is 1 July 2008 to 30 June 2009, countries will include patients who started antiretroviral therapy from 1 July 2007 to 30 June 2008. A 12-month outcome is defined as the outcome (i.e., whether the patient is still alive and on antiretroviral therapy, dead or lost to follow-up) at 12 months after starting therapy. For example, patients who started antiretroviral therapy during the 12-month period from 1 January to 31 December 2007 will have reached their 12-month outcomes for the reporting period of 1 January to 31 December 2008.
Data Collection
Data Collection Method: 
Patient record
Programme records
Measurement Frequency: 
Continuously
Epidemic Type: 
Concentrated/low level
Generalized
Indicator Type: 
Programme / Service Delivery
Indicator Level: 
National
Disaggregations
Education: 
N/A
Age-group: 
< (less than) 15 years
> (greater than) 15 years
Gender: 
Female
Male
Geographic Location: 
N/A
Pregnancy: 
N/A
Sector: 
N/A
Target: 
N/A
Time Period: 
N/A
Type of Orphan: 
N/A
Vulnerability Status: 
N/A
HIV Status: 
N/A
Service Type: 
N/A
Condom Type: 
N/A
Strengths and weaknesses: 

Using this denominator may underestimate true “survival”, since a proportion of those lost to follow-up
are alive. The number of people alive and on antiretroviral therapy (i.e. retention on antiretroviral therapy)
in a treatment cohort is captured here.

Priority reporting is for aggregate survival reporting. If comprehensive cohort patient registries are
available then it is encouraged for countries to track retention on treatment at 24, 36, and 48 months
and yearly thereafter. This will enable comparison over time of survival on antiretroviral therapy. As it
stands, it is possible to identify whether survival at 12 months increases or decreases over time. However, it is not possible to attribute cause to these changes. For example, if survival at 12 months increases over time, this may reflect an improvement in care and treatment practices or earlier initiation of antiretroviral therapy. The retention on antiretroviral therapy at 12 months therefore needs to be interpreted in view of the baseline characteristics of the cohort of patients at the start of antiretroviral therapy: mortality will be higher in sites where patients accessed antiretroviral therapy at a later stage of infection. Therefore, collection and reporting of survival over longer durations of treatment outcomes may provide a better picture of the long-term effectiveness of antiretroviral therapy.

Preferred Indicator: 
Core National Indicator - UNGASS
Agency: 
Joint United Nations Programme on HIV/AIDS (UNAIDS)
The President's Emergency Plan for AIDS Relief (PEPFAR)
World Health Organisation (WHO)
Relevance: 
2009 UN General Assembly Special Session on HIV/AIDS (UNGASS)
3 by 5
Universal Access (UA)
US President's Emergency Plan for AIDS Relief (PEPFAR)
Status: 
Active
Keywords
Programme Focus General: 
Treatment
Programme Focus Specific: 
Antiretroviral Therapy (ART)
Target Population: 
People Living with HIV
Sex: All
Age: Not Specified
Patients: ART
Goal - Initiative or Country: 
Initiative

Most-at-risk Populations: Reduction in HIV Prevalence

Percentage of most-at-risk populations who are HIV-infected

Alias: 
UNICEF: HIV prevalence among most-at-risk populations WHO Universal Access: % of MARPS who are HIV infected
ID: 
668
What it measures: 

To assess progress on reducing HIV prevalence among most-at-risk populations
Most-at-risk populations typically have the highest HIV prevalence in countries with either concentrated
or generalized epidemics. In many cases, prevalence among these populations can be more than double the prevalence among the general population. Reducing prevalence among most-at-risk populations is a critical measure of a national-level response to HIV. This indicator should be calculated separately for each population that is considered most-at-risk in a given country: sex workers, injecting drug users, men who have sex with men.

Note: countries with generalized epidemics may also have a concentrated subepidemic among one or
more most-at-risk population. If so, it would be valuable for them to calculate and report on this indicator
for those populations.
 

Numerator: 

Number of members of most-at-risk population who test positive for HIV

Denominator: 

Number of members of most-at-risk population tested for HIV

Data Type: 
Percent
Unit: 
N/A
Multiplier: 
N/A
Composite Indicator: 
No
Calculation: 
Numerator / Denominator
Method of measurement: 
This indicator is calculated using data from HIV tests conducted among members of most-at-risk population groups in the primary sentinel site or sites. The sentinel surveillance sites used for the calculation of this indicator should remain constant to allow for the tracking of changes over time. In theory, assessing progress in reducing the occurrence of new infections is best done through monitoring changes in incidence over time. However, in practice, prevalence data rather than incidence data are available. In analysing prevalence data of most-at-risk-populations for the assessment of prevention programme impact, it is desirable not to restrict analysis to young people but to report on those persons who are newly initiated to behaviours that put them at risk for infection (e.g. by restricting the analysis to people who have initiated injecting drug use within the last year or participated in sex work for less than one year, etc.). This type of restricted analysis will also have the advantage of not being affected by the effect of antiretroviral therapy in increasing survival and thereby increasing prevalence. In the Country Progress Report, it is imperative to indicate whether this type of analysis is used to allow for meaningful global analysis.  
Data Collection
Data Collection Method: 
HIV sero-sentinel surveillance
Measurement Frequency: 
Annual
Epidemic Type: 
Concentrated/low level
Generalized
Indicator Type: 
Disease Impact
Indicator Level: 
National
Disaggregations
Education: 
N/A
Gender: 
Female
Male
Geographic Location: 
N/A
Pregnancy: 
N/A
Sector: 
N/A
Target: 
N/A
Time Period: 
N/A
Type of Orphan: 
N/A
Vulnerability Status: 
N/A
HIV Status: 
N/A
Service Type: 
N/A
Condom Type: 
N/A
Strengths and weaknesses: 

 Due to diffi culties in accessing most-at-risk populations, biases in serosurveillance data are likely to be far more significant than in data from a more general population, such as women attending antenatal clinics. If there are concerns about the data, these concerns should be reflected in the interpretation.

An understanding of how the sampled population(s) relate to any larger population(s) sharing similar risk behaviours is critical to the interpretation of this indicator. The period during which people belong to a most-at-risk population is more closely associated with the risk of acquiring HIV than age. Therefore, it is desirable not to restrict analysis to young people but to report on other age groups as well.
Trends in HIV prevalence among most-at-risk populations in the capital city will provide a useful indication of HIV-prevention programme performance in that city. However, it will not be representative of the situation in the country as a whole.

The addition of new sentinel sites will increase the samples representativeness and will therefore give a
more robust point estimate of HIV prevalence. However, the addition of new sentinel sites reduces the
comparability of values. As such it is important to exclude new sites from the calculation of this indicator
when undertaking trend analyses.

Revised guidelines on HIV surveillance on most-at-risk populations are currently being prepared by the
WHO/UNAIDS Global Working Group on STI/HIV Surveillance. For further information please refer
to: http://www.unaids.org/en/KnowledgeCentre/HIVData/Epidemiology/default.asp.
 

Preferred Indicator: 
Core National Indicator - UNGASS
Agency: 
Joint United Nations Programme on HIV/AIDS (UNAIDS)
The President's Emergency Plan for AIDS Relief (PEPFAR)
United Nations Children's Fund (UNICEF)
World Health Organisation (WHO)
Relevance: 
2009 UN General Assembly Special Session on HIV/AIDS (UNGASS)
Universal Access (UA)
US President's Emergency Plan for AIDS Relief (PEPFAR)
Status: 
Active
Keywords
Programme Focus General: 
Prevention
Programme Focus Specific: 
HIV Prevalence
Target Population: 
Most-at-Risk: All
Sex: All
Age: Not Specified
Goal - Initiative or Country: 
Initiative

Reduction in HIV prevalence

Percentage of young people aged 15–24 who are HIV infected

Alias: 
WHO (Youth): HIV prevalence among young pregnant women UNICEF: HIV prevalence among pregnant women 15-24 years, capital city
ID: 
667
What it measures: 

To assess progress towards reducing HIV infection.

The goal in the response to HIV is to reduce HIV infection. As the highest rates of new HIV infections
typically occur in young adults, more than 180 countries have committed themselves to achieving major
reductions in HIV prevalence among young people—a 25% reduction in the most affected countries by
2005 and a 25% reduction globally by 2010.
 

Numerator: 

Number of antenatal clinic attendees (aged 15–24) tested whose HIV test results are positive

Denominator: 

Number of antenatal clinic attendees (aged 15–24) tested for their HIV infection status

Data Type: 
Percent
Unit: 
N/A
Multiplier: 
N/A
Composite Indicator: 
No
Calculation: 
Numerator / Denominator
Method of measurement: 
This indicator is calculated using data from pregnant women attending antenatal clinics in HIV sentinel surveillance sites in the capital city, other urban areas and rural areas.  The sentinel surveillance sites used for the calculation of this indicator should remain constant to allow for the tracking of changes over time. The proportion of the total female population aged 15–24 living in the capital city, in other urban areas and in rural areas should be provided so that national estimates can be calculated, where possible.
Data Collection
Data Collection Method: 
HIV sero-sentinel surveillance
Measurement Frequency: 
Annual
Epidemic Type: 
Generalized
Indicator Type: 
Disease Impact
Indicator Level: 
National
Disaggregations
Education: 
N/A
Gender: 
N/A
Geographic Location: 
Capital City
Rural
Urban
Pregnancy: 
N/A
Sector: 
N/A
Target: 
N/A
Time Period: 
N/A
Type of Orphan: 
N/A
Vulnerability Status: 
N/A
HIV Status: 
N/A
Service Type: 
N/A
Condom Type: 
N/A
Strengths and weaknesses: 

HIV prevalence at any given age is the difference between the cumulative numbers of people that have
become infected with HIV up to this age minus the number who have died, expressed as a percentage of the total number alive at this age. At older ages, changes in HIV prevalence are slow to reflect changes in the rate of new infections (HIV incidence) because the average duration of infection is long. Furthermore, declines in HIV prevalence can refl ect saturation of infection among those individuals who are most vulnerable and rising mortality rather than behaviour change. At young ages, trends in HIV prevalence are a better indication of recent trends in HIV incidence and risk behaviour. Thus, reductions in HIV incidence associated with genuine behaviour change should first become detectable in HIV prevalence figures for 15–19-year-olds. Where available, parallel behavioural surveillance survey data should be used to aid interpretation of trends in HIV prevalence.

In countries where the age at which young people first have sexual intercourse is late and/or levels of
contraception use are high, HIV prevalence among pregnant women of 15–24 years of age will differ from that among all women in the age group.

This indicator (using data from antenatal clinics) gives a fairly good estimate of relatively recent trends in
HIV infection in locations where the epidemic is heterosexually driven. It is less reliable as an indicator
of HIV-epidemic trends in locations where most infections remain temporarily confined to most-at-risk
populations.

To supplement data from antenatal clinics, an increasing number of countries have included HIV testing
in population-based surveys. If a country has produced HIV prevalence estimates from survey data these
estimates should be included in the comments box for this indicator to allow for comparisons between
multiple surveys. If available, survey based estimates should be disaggregated by sex.

The addition of new sentinel sites will increase the samples representativeness and will therefore give a
more robust point estimate of HIV prevalence. However, the addition of new sentinel sites reduces the
comparability of values. As such it is important to exclude new sites from the calculation of this indicator
when undertaking trend analyses.
 

Preferred Indicator: 
Core National Indicator - UNGASS
Agency: 
Joint United Nations Programme on HIV/AIDS (UNAIDS)
The President's Emergency Plan for AIDS Relief (PEPFAR)
United Nations Children's Fund (UNICEF)
United Nations Development Group (UNDG)
World Bank (WB)
World Health Organisation (WHO)
Relevance: 
2009 UN General Assembly Special Session on HIV/AIDS (UNGASS)
Millenium Development Goals (MDG)
Universal Access (UA)
US President's Emergency Plan for AIDS Relief (PEPFAR)
Status: 
Active
Keywords
Programme Focus General: 
Prevention
Programme Focus Specific: 
HIV Prevalence
Site / Setting: 
Health Care Setting
Rural Site
Urban Site
Target Population: 
Age: Young People
Sex: Women Only
Goal - Initiative or Country: 
Initiative

Injecting Drug Users: Safe Injecting Practices

Percentage of injecting drug users reporting the use of sterile injecting equipment the last time they injected

ID: 
666
What it measures: 

 To assess progress in preventing injecting drug use-associated HIV transmission.
Safer injecting and sexual practices among injecting drug users are essential, even in countries where other modes of HIV transmission predominate, because: (i) the risk of HIV transmission from contaminated injecting equipment is extremely high; and (ii) injecting drug users can spread HIV (e.g., through sexual transmission) to the wider population.

Note: countries with generalized epidemics may also have a concentrated sub-epidemic among injecting drug users. If so, it would be valuable for them to calculate and report on this indicator for this population.
 

Numerator: 

 Number of respondents who report using sterile injecting equipment the last time they injected drugs
 

Denominator: 

 Number of respondents who report injecting drugs in the last month
 

Data Type: 
Percent
Unit: 
N/A
Multiplier: 
N/A
Composite Indicator: 
No
Calculation: 
Numerator / Denominator
Method of measurement: 
 Respondents are asked the following questions. 1. Have you injected drugs at any time in the last month? 2. If yes: The last time you injected drugs, did you use a sterile needle and syringe? Whenever possible, data for injecting drug users should be collected through civil society organizations that have worked closely with this population in the field. Access to survey respondents as well as the data collected from them must remain confidential.
Data Collection
Data Collection Method: 
Survey: most-at-risk population
Data Collection Tools: 
Behavioural Surveillance Survey (BSS)
Measurement Frequency: 
Biennial
Epidemic Type: 
Concentrated/low level
Generalized
Indicator Type: 
Behavioral Outcome
Indicator Level: 
National
Disaggregations
Education: 
N/A
Age-group: 
< (less than) 25 years
> (greater than) 25 years
Gender: 
Female
Male
Geographic Location: 
N/A
Pregnancy: 
N/A
Sector: 
N/A
Target: 
N/A
Time Period: 
N/A
Type of Orphan: 
N/A
Vulnerability Status: 
N/A
HIV Status: 
N/A
Service Type: 
N/A
Condom Type: 
N/A
Strengths and weaknesses: 

 Surveying injecting drug users can be challenging. Consequently, data obtained may not be based on a
representative sample of the national injecting drug user population being surveyed. If there are concerns that the data are not based on a representative sample, these concerns should be refl ected in the interpretation of the survey data. Where different sources of data exist, the best available estimate should be used. Information on the sample size, the quality and reliability of the data, and any related issues should be included in the report submitted with this indicator.

The extent of injecting drug use-associated HIV transmission within a country depends on four factors:
(i) the size, stage and pattern of dissemination of the national AIDS epidemic; (ii) the extent of injecting
drug use; (iii) the degree to which injecting drug users use contaminated injecting equipment; and (iv) the patterns of sexual mixing and condom use among injecting drug users and between injecting drug users and the wider population. This indicator provides information on the third factor.

To maximize the utility of these data, it is recommended that the same sample used for the calculation of
this indicator be used for the calculation of the other indicators related to these populations.

Preferred Indicator: 
Core National Indicator - UNGASS
Agency: 
Joint United Nations Programme on HIV/AIDS (UNAIDS)
The President's Emergency Plan for AIDS Relief (PEPFAR)
Relevance: 
2009 UN General Assembly Special Session on HIV/AIDS (UNGASS)
US President's Emergency Plan for AIDS Relief (PEPFAR)
Status: 
Active
Keywords
Programme Focus General: 
Prevention
Programme Focus Specific: 
Injecting Behaviour
Target Population: 
Most-at-Risk: Injecting Drug Users
Sex: All
Age: Not Specified
Goal - Initiative or Country: 
Initiative

Injecting Drug Users: Condom Use

Percentage of injecting durg users reporting the use of a condom the last time they had sexual intercourse

ID: 
665
What it measures: 

 To assess progress in preventing sexual transmission of HIV.

Safer injecting and sexual practices among injecting drug users are essential, even in countries where other modes of HIV transmission predominate, because: (i) the risk of HIV transmission from contaminated injecting equipment is extremely high; and (ii) injecting drug users can spread HIV (e.g. through sexual transmission) to the wider population.

Note: countries with generalized epidemics may also have a concentrated subepidemic among injecting
drug users. If so, it would be valuable for them to calculate and report on this indicator for this population.
 

Numerator: 

Number of respondents who reported that a condom was used the last time they had sex

Denominator: 

Number of respondents who report having injected drugs and having had sexual intercourse in the last month

Data Type: 
Percent
Unit: 
N/A
Multiplier: 
N/A
Composite Indicator: 
No
Calculation: 
Numerator / Denominator
Method of measurement: 
Respondents are asked the following sequence of questions. 1. Have you injected drugs at any time in the last month? 2. If yes: have you had sexual intercourse in the last month? 3. If yes in answer to both 1 and 2: did you use a condom when you last had sexual intercourse? Whenever possible, data for injecting drug users should be collected through civil society organizations that have worked closely with this population in the field. Access to survey respondents as well as the data collected from them must remain confi dential.
Data Collection
Data Collection Method: 
Survey: most-at-risk population
Data Collection Tools: 
Behavioural Surveillance Survey (BSS)
Measurement Frequency: 
Biennial
Epidemic Type: 
Concentrated/low level
Generalized
Indicator Type: 
Behavioral Outcome
Indicator Level: 
National
Disaggregations
Education: 
N/A
Age-group: 
< (less than) 25 years
> (greater than) 25 years
Gender: 
Female
Male
Geographic Location: 
N/A
Pregnancy: 
N/A
Sector: 
N/A
Target: 
N/A
Time Period: 
N/A
Type of Orphan: 
N/A
Vulnerability Status: 
N/A
HIV Status: 
N/A
Service Type: 
N/A
Condom Type: 
N/A
Strengths and weaknesses: 

Surveying injecting drug users can be challenging. Consequently, data obtained may not be based on a
representative sample of the national injecting drug user population being surveyed. If there are concerns
that the data are not based on a representative sample, these concerns should be refl ected in the interpretation of the survey data. Where different sources of data exist, the best available estimate should be used. Information on the sample size, the quality and reliability of the data, and any related issues should be included in the report submitted with this indicator.
 The extent of injecting drug use-associated HIV transmission within a country depends on four factors:
(i) the size, stage and pattern of dissemination of the national AIDS epidemic; (ii) the extent of injecting
drug use; (iii) the degree to which injecting drug users use contaminated injecting equipment; and (iv) the patterns of sexual mixing and condom use among injecting drug users and between injecting drug users and the wider population. This indicator provides partial information on the fourth factor.

To maximize the utility of these data, it is recommended that the same sample used for the calculation of
this indicator be used for the calculation of the other indicators related to these populations.

Preferred Indicator: 
Core National Indicator - UNGASS
Agency: 
Joint United Nations Programme on HIV/AIDS (UNAIDS)
The President's Emergency Plan for AIDS Relief (PEPFAR)
Relevance: 
2009 UN General Assembly Special Session on HIV/AIDS (UNGASS)
US President's Emergency Plan for AIDS Relief (PEPFAR)
Status: 
Active
Keywords
Programme Focus General: 
Prevention
Programme Focus Specific: 
Sexual Behaviour
Condoms
Target Population: 
Most-at-Risk: Injecting Drug Users
Sex: All
Age: Not Specified
Goal - Initiative or Country: 
Initiative

Men Who Have Sex with Men: Condom Use

Percentage of men reporting the use of a condom the last time they had anal sex with a male partner

Alias: 
UNICEF: Condom use among men who have sex with men UNAIDS (2000): Condom use at last anal sex between men
ID: 
664
What it measures: 

 It measures progress in preventing exposure to HIV among men who have unprotected anal sex with a male partner.

Condoms can substantially reduce the risk of the sexual transmission of HIV. Consequently, consistent and correct condom use is important for men who have sex with men because of the high risk of HIV transmission during unprotected anal sex. In addition, men who have anal sex with other men may also have female partners, who could become infected as well. Condom use with their most recent male partner is considered a reliable indicator of longer-term behaviour.

Note: countries with generalized epidemics may also have a concentrated subepidemic among men who have sex with men. If so, it would be valuable for them to calculate and report on this indicator for this population.
 

Numerator: 

Number of respondents who reported that a condom was used the last time they had anal sex

This includes both regular and non-regular partners, and both paid and unpaid sex. As with all indicators this indicator only provides a limited piece of information. For a comprehensive assessment of patterns of risk associated with male to male sex further information is needed, including information on the types and numbers of partners and whether the individual is the receptive or insertive partner.

Denominator: 

Number of respondents who reported having had anal sex with a male partner in the last six months

Data Type: 
Percent
Unit: 
N/A
Multiplier: 
N/A
Calculation: 
Numerator / Denominator
Method of measurement: 
In a behavioural survey of a sample of men who have sex with men, respondents are asked about sexual partnerships in the preceding six months, about anal sex within those partnerships and about condom use when they last had anal sex. Whenever possible, data for men who have sex with men should be collected through civil society organizations that have worked closely with this population in the field. Access to survey respondents as well as the data collected from them must remain confidential.  
Data Collection
Data Collection Method: 
Survey: most-at-risk population
Data Collection Tools: 
Behavioural Surveillance Survey (BSS)
Measurement Frequency: 
Biennial
Epidemic Type: 
Concentrated/low level
Generalized
Indicator Type: 
Behavioral Outcome
Indicator Level: 
National
Disaggregations
Age-group: 
< (less than) 25 years
> (greater than) 25 years
Strengths and weaknesses: 

 For men who have sex with men, condom use at last anal sex with any partner gives a good indication of overall levels and trends of protected and unprotected sex in this population. This indicator does not give any idea of risk behaviour in sex with women among men who have sex with both women and men.
In countries where men in the subpopulation surveyed are likely to have partners of both sexes, condom
use with female as well as male partners should be investigated. In these cases, data on condom use should always be presented separately for female and male partners.

This indicator asks about male-to-male sex in the past six months. If you have data available on another
time period, such as the last 3 or 12 months, please include this additional data in the comments section of the reporting tool.

Surveying men who have sex with men can be challenging. Consequently, data obtained may not be based on a representative sample of the national, most-at-risk population being surveyed. If there are concerns that the data are not based on a representative sample, these concerns should be reflected in the interpretation of the survey data. Where different sources of data exist, the best available estimate should be used. Information on the sample size, the quality and reliability of the data, and any related issues should be included in the report submitted with this indicator.

To maximize the utility of these data, it is recommended that the same sample used for the calculation of
this indicator be used for the calculation of the other indicators related to these populations.

Preferred Indicator: 
Core National Indicator - UNGASS
Global AIDS Progress Reporting 2012
Agency: 
European Centre for Disease Prevention and Control (ECDC)
Global Fund to Fight AIDS, Tuberculosis and Malaria (GFATM)
Joint United Nations Programme on HIV/AIDS (UNAIDS)
The President's Emergency Plan for AIDS Relief (PEPFAR)
United Nations Children's Fund (UNICEF)
Relevance: 
2009 UN General Assembly Special Session on HIV/AIDS (UNGASS)
Dublin Declaration Monitoring
Global AIDS Progress Reporting 2012
Global AIDS Response Progress Reporting (GARPR) 2013
Universal Access (UA)
US President's Emergency Plan for AIDS Relief (PEPFAR)
Status: 
Active
Keywords
Programme Focus General: 
Prevention
Programme Focus Specific: 
Behaviour Change
Sexual Behaviour
Condoms
Target Population: 
Most-at-Risk: Men who have Sex with Men
Sex: Men Only
Age: Adults
Age: Young People
Goal - Initiative or Country: 
Initiative

Sex Workers: Condom Use

Percentage of female and male sex workers reporting the use of a condom with their most recent client.

Alias: 
UNAIDS (2000): Condom use at last commerical sex, sex worker report
ID: 
663
What it measures: 

It measures progress in preventing exposure to HIV among sex workers through unprotected sex with clients.

Various factors increase the risk of exposure to HIV among sex workers, including multiple, non-regular
partners and more frequent sexual intercourse. However, sex workers can substantially reduce the risk of HIV transmission, both from clients and to clients, through consistent and correct condom use.

Note: Countries with generalized epidemics may also have a concentrated subepidemic among sex workers. If so, it would be valuable for them to calculate and report on this indicator for this population.
 

Numerator: 

Number of respondents who reported that a condom was used with their last client

Denominator: 

Number of respondents who reported having commercial sex in the last 12 months

Data Type: 
Percent
Calculation: 
Numerator / Denominator
Method of measurement: 
Respondents are asked the following question: Did you use a condom with your most recent client? Whenever possible, data for sex workers should be collected through civil society organizations that have worked closely with this population in the field. Access to survey respondents as well as the data collected from them must remain confidential. For further information, please consult the following references: o UNAIDS (2007). A Framework for Monitoring and Evaluating HIV Prevention Programmes for Most-At-Risk Populations. Geneva: UNAIDS. o UNAIDS (2007). Practical Guidelines for Intensifying HIV Prevention: Towards Universal Access. Geneva:UNAIDS.
Data Collection
Data Collection Method: 
Survey: most-at-risk population
Data Collection Tools: 
Behavioural Surveillance Survey (BSS)
Measurement Frequency: 
Biennial
Epidemic Type: 
Concentrated/low level
Generalized
Indicator Type: 
Behavioral Outcome
Indicator Level: 
National
Disaggregations
Age-group: 
< (less than) 25 years
> (greater than) 25 years
Gender: 
Female
Male
Strengths and weaknesses: 

Condoms are most effective when their use is consistent, rather than occasional. The current indicator
will provide an overestimate of the level of consistent condom use. However, the alternative method of
asking whether condoms are always/sometimes/never used in sexual encounters with clients in a specified period is subject to recall bias. Furthermore, the trend in condom use in the most recent sexual act will generally reflect the trend in consistent condom use.

This indicator asks about commercial sex in the past twelve months. If you have data available on another time period, such as the last 3 or 6 months, please include this additional data in the comments section of the reporting tool.
 Surveying sex workers can be challenging. Consequently, data obtained may not be based on a representative sample of the national, most-at-risk population being surveyed. If there are concerns that the data are not based on a representative sample, these concerns should be refl ected in the interpretation of the survey data. Where different sources of data exist, the best available estimate should be used. Information on the sample size, the quality and reliability of the data, and any related issues should be included in the report submitted with this indicator.

To maximize the utility of these data, it is recommended that the same sample used for the calculation of
this indicator be used for the calculation of the other indicators related to these populations.

Preferred Indicator: 
Core National Indicator - UNGASS
Global AIDS Progress Reporting 2012
Agency: 
European Centre for Disease Prevention and Control (ECDC)
Global Fund to Fight AIDS, Tuberculosis and Malaria (GFATM)
Joint United Nations Programme on HIV/AIDS (UNAIDS)
The President's Emergency Plan for AIDS Relief (PEPFAR)
United Nations Children's Fund (UNICEF)
Relevance: 
2009 UN General Assembly Special Session on HIV/AIDS (UNGASS)
Dublin Declaration Monitoring
Global AIDS Progress Reporting 2012
Global AIDS Response Progress Reporting (GARPR) 2013
Universal Access (UA)
US President's Emergency Plan for AIDS Relief (PEPFAR)
Status: 
Active
Keywords
Programme Focus General: 
Prevention
Programme Focus Specific: 
Behaviour Change
Sexual Behaviour
Condoms
Target Population: 
Most-at-Risk: Sex Workers
Sex: All
Age: Not Specified
Goal - Initiative or Country: 
Initiative
Syndicate content