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Spatial clusters of gonorrhoea in England with particular reference to the outcome of partner notification: 2012 and 2013

  • Allen O’Brien ,

    Roles Conceptualization, Formal analysis, Investigation, Methodology, Project administration, Software, Validation, Visualization, Writing – original draft, Writing – review & editing

    allen.obrien@ubc.ca

    Current address: School of Engineering, University of British Columbia, Kelowna, BC, Canada

    Affiliation Department of Global Health and Development, London School of Hygiene and Tropical Medicine, London, United Kingdom

  • Ellie Sherrard-Smith,

    Roles Conceptualization, Methodology, Resources, Supervision, Writing – review & editing

    Current address: MRC Centre for Outbreak Analysis and Modelling, Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom

    Affiliation HIV and STI Department, National Infection Service, Public Health England, London, United Kingdom

  • Bersabeh Sile,

    Roles Data curation, Resources, Software, Writing – review & editing

    Affiliation HIV and STI Department, National Infection Service, Public Health England, London, United Kingdom

  • Charlotte Watts,

    Roles Conceptualization, Project administration, Supervision, Writing – review & editing

    Affiliation Department of Global Health and Development, London School of Hygiene and Tropical Medicine, London, United Kingdom

  • Ian Simms

    Roles Conceptualization, Project administration, Resources, Supervision, Writing – review & editing

    Affiliation HIV and STI Department, National Infection Service, Public Health England, London, United Kingdom

Abstract

Background

This study explored spatial-temporal variation in diagnoses of gonorrhoea to identify and quantify endemic areas and clusters in relation to patient characteristics and outcomes of partner notification (PN) across England, UK.

Methods

Endemic areas and clusters were identified using a two-stage analysis with Kulldorff’s scan statistics (SaTScan).

Results

Of 2,571,838 tests, 53,547 diagnoses were gonorrhoea positive (positivity = 2.08%). The proportion of diagnoses in heterosexual males was 1.5 times that in heterosexual females. Among index cases, men who have sex with men (MSM) were 8 times more likely to be diagnosed with gonorrhoea than heterosexual males (p<0.0001). After controlling for age, gender, ethnicity and deprivation rank, 4 endemic areas were identified including 11,047 diagnoses, 86% of which occurred in London. 33 clusters included 17,629 diagnoses (34% of total diagnoses in 2012 and 2013) and spanned 21 locations, some of which were dominated by heterosexually acquired infection, whilst others were MSM focused. Of the 53,547 diagnoses, 14.5% (7,775) were the result of PN. The proportion of patients who attended services as a result of PN varied from 0% to 61% within different age, gender and sexual orientation cohorts. A third of tests resulting from PN were positive for gonorrhoea. 25% of Local Authorities (n = 81, 95% CI: 20.2, 29.5) had a higher than expected proportion for female PN diagnoses as compared to 16% for males (n = 52, 95% CI: 12.0, 19.9).

Conclusions

The English gonorrhoea epidemic is characterised by spatial-temporal variation. PN success varied between endemic areas and clusters. Greater emphasis should be placed on the role of PN in the control of gonorrhoea to reduce the risk of onward transmission, re-infection, and complications of infection.

Introduction

Neisseria gonorrhoeae, the causative agent of gonorrhoea, is the second most common bacterial sexually transmitted infection (STI) diagnosed in England. Gonorrhoea diagnoses reached their nadir in the early 1990s (approximately 10,000 in 1993), rose to 41,262 (2015) and subsequently fell to 36,244 in 2016 [1]. The epidemic has been focused on core risk groups including men who have sex with men (MSM), accounting for 49% of diagnoses (17,584) in 2016, and black Caribbeans [2,3]. Infection is also geographically concentrated and strongly associated with deprivation [4,5]. Transmission is perpetuated by higher rates of partner change and complex sexual networks, which can lead to localised outbreaks such as that observed recently amongst young heterosexuals [6,7]. In addition, there has been increasing concern over emerging antimicrobial resistance in gonorrhoea which threatens effective treatment and infection control strategies [812].

In England, sexual health services for the confidential diagnosis, treatment and management of STIs are provided free of charge. Partner notification (PN), including provider referral and outcome follow-up, is an essential control strategy as it reduces the risk of onward transmission, re-infection, and complications [13,14]. Since 2012, information concerning PN has been collected through the Genitourinary Medicine Clinic Activity Dataset (GUMCAD) surveillance system. Here we explore the characteristics of gonorrhoea clusters and endemic areas across England using space-time analytical techniques.

Materials and methods

Data sources

All commissioned sexual health services are required to report STI tests and diagnoses to Public Health England (PHE) through GUMCAD. The latest iteration of GUMCAD includes reporting through community pharmacies and internet testing; however, when this project was undertaken testing activity and diagnoses made through such services were not captured unless patients were referred to a commissioned or specialist service for ongoing management. Diagnoses of gonorrhoea were extracted from GUMCAD for 2012 and 2013 [15]. This pseudo-anonymised disaggregate dataset included information on patient age, gender, ethnicity, country of birth, sexual orientation, STI testing and diagnoses, HIV status, clinic attended, and attendance date. Diagnoses were coded as either index or partner notified. A positive diagnosis was considered partner notified if the diagnosis occurred 42 days before or after PN, otherwise it was classified as an index case. This timeframe ensured the study captured individuals who may have experienced symptoms after contact with an index case, even if they were tested for other reasons before PN or delayed clinical attendance. A male or female patient positive for gonorrhoea after attending sexual health services due to PN was defined as a male or female PN diagnosis, respectively.

Clinic and patient location were analysed at two geographic area levels: Middle Super Output Area (MSOA; n = 6,791, population range 5,000 to 15,000) and lower tier Local Authority (LA; n = 326, population range 2,224 to 1,074,283) [1517]. Population denominators for gender, age, and ethnicity available at MSOA and LA levels were used to calculate testing coverage and diagnosis rate [18]. A population denominator for sexual orientation was not available. The Index of Multiple Deprivation (IMD) classification, grouped by quintile, was included [19].

Diagnoses, including repeat infections (restricted to one positive diagnosis every 42 days), were stratified by gender, age, ethnicity, sexual orientation, region of birth, and HIV status. During the study period some individuals transitioned between age groups. Consequently, 2,489,334 subjects were identified across the age groups compared to 2,420,090 unique individuals. To explore gonorrhoea positivity (proportion of tests which tested positive) the dataset was restricted to those attending for gonorrhoea tests.

Analyses were based on de-identified surveillance data held by PHE. In its role providing infectious disease surveillance, PHE has permission to handle data obtained by GUMCAD under Regulation 3 of the Health Service (Control of Patient Information) Regulations 2002. The London School of Hygiene and Tropical Medicine Research Ethics Committee granted ethical approval on June 5th 2014 (Project ID: 7578).

Statistical analyses

Descriptive analyses.

The crude diagnosis rate (not controlled for covariates) was calculated for each LA. To be comparable with the demarcations used in PHE STI profiles in previous years, areas with a diagnosis rate 20% above the England average were classified as having a high rate of infection, whereas those 20% below had a low rate [20].

To examine spatial-temporal patterns the data were classified by quarter. The expected quarterly diagnosis rate was derived from the total diagnosis rate for 2012 and 2013 and was assumed to be evenly distributed. Gonorrhoea clusters were investigated by MSOA regions to provide greater detail on spatial-temporal patterns that were otherwise masked at the LA level. The proportion of PN diagnoses in each LA was calculated by comparing the number of PN diagnoses per LA to the national total of all gonorrhoea diagnoses. The observed proportion of PN diagnoses within each LA was then compared to the expected proportion of 0.045% (i.e., the proportion of PN diagnoses if evenly distributed across all LAs).

Detection and analysis of endemic areas and clusters.

Endemic areas consisted of MSOAs that had a high diagnosis rate for every six month period in 2012 and 2013. To avoid large endemic areas masking small clusters a two-stage procedure was used [21]. After endemic areas had been excluded, potential clusters were identified using a retrospective spatial-temporal SaTScan analysis (S1 Text) [22]. A likelihood ratio test was performed for each cluster, comparing the expected diagnoses from a Poisson distribution to those actually observed inside versus outside the boundary. Potential clusters were detected at the 95% confidence level and a discrete Poisson model was used to adjust for age, gender, ethnicity, and IMD rank. Population weighted centroids for each MSOA were used to identify clusters containing up to 1% of the population instead of the SaTScan 50% default setting [21]. Data for MSOAs contained within a cluster were aggregated. Clusters were then compared in terms of gender, sexual orientation, and PN classification (index or PN diagnosis). Here the locations have been referred to using local place names. When stratified by cluster location, women who have sex with women (WSW) presented low numbers of diagnoses and were grouped with heterosexuals to form a single female category. Data analysis was conducted in SaTScan v9.2 and STATA13 [23,24].

Results

Descriptive analysis

Between 2012 and 2013, 2,420,090 patient attendances were recorded in GUMCAD (Table 1). Of the 2,571,838 gonorrhoea tests performed, 53,547 (2.08%, 95% CI: 2.06, 2.10) were positive. A gradual increase in the proportion of positive gonorrhoea diagnoses was observed over 2012 and 2013.The highest number of patients attending GUM services was seen in the 20–34 year age group (62%). Gonorrhoea positivity was 3 times higher among males (3.27%) as compared to females (1.04%), primarily due to higher rates among MSM. Positive gonorrhoea diagnoses in both MSM (11.7%) and HIV positive patients (12.5%) were over 5 times higher than the average for all gonorrhoea tests performed. Although WSW had the fewest gonorrhoea diagnoses (86/5,097 tests), positivity (1.69%, 95% CI: 1.35, 2.08) in this group was slightly higher than heterosexual females (1.04%, 95% CI: 1.02, 1.05).

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Table 1. Patients attending GUM clinics and diagnoses of gonorrhoea, England: 2012 to 2013.

https://doi.org/10.1371/journal.pone.0195178.t001

The crude diagnosis rate was 100.8/100,000 individuals. Highest diagnosis rates were seen in LAs within cities, including London, Manchester, Newcastle-upon-Tyne, Brighton, Bedford, and Leeds (S1 Fig). Diagnosis rates of over 120/100,000 were seen in 43 LAs but the number of LAs with high rates varied by gender: more LAs with high rates were observed among males (n = 61) than females (n = 13) (S2 Fig). LAs with high rates of male diagnoses were also more geographically dispersed.

The expected average quarterly diagnosis rate for England was 12.6/100,000 individuals. LAs in London, Brighton, Manchester, and Newcastle-upon-Tyne had persistently high diagnosis rates (>12.6/100,000) across quarters (i.e. three month intervals) whereas diagnoses in surrounding LAs fluctuated (Fig 1). Spatial patterns seen at MSOA level (S3 Fig) generally reflected diagnosis rates seen at LA level, a pattern observed in both 2012 and 2013.

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Fig 1. Quarterly gonorrhoea diagnosis rate with regions grouped by Local Authority (LA), England: 2013.

Regions are compared to the English average (12.6/100,000 people) as higher, similar or lower. Similar regions were denoted as those within 20% above or below the English average (12.6–15.1 and 10.1–12.6/100,000 people, respectively).

https://doi.org/10.1371/journal.pone.0195178.g001

Partner notification analysis

Of the 53,547 positive gonorrhoea tests, 45,772 (85.5%) were index cases and 14.5% (7,775) were diagnosed as a result of PN. Among index cases, the proportion of gonorrhoea positive males was 3.2 times higher than females (p<0.0001). Approximately a third of PN diagnoses were gonorrhoea positive, which is consistent with PHE annual data tables [2]. The observed proportion of PN diagnoses in each LA (calculated from the national total of gonorrhoea diagnoses) was compared to the expected proportion of 0.045% (the proportion of PN diagnoses if distributed evenly across all LAs) (S4 Fig). Female PN diagnoses outweighed male PN diagnoses across LAs; 25% of LAs (n = 81, 95% CI: 20.2, 29.5) had a higher than expected proportion for female PN diagnoses compared to 16% for males (n = 52, 95% CI: 12.0, 19.9).

Endemic areas and clusters

After controlling for age, gender, ethnicity, and IMD rank, endemic areas were identified in 232 MSOAs (3.7% of England’s population) within 4 cities: London, Brighton, Birmingham and Manchester (Fig 2). These endemic areas included 11,047 gonorrhoea diagnoses (22% of total diagnoses in 2012 and 2013), 86% of which occurred in London (Table 2). A total of 33 clusters were identified across 1,137 MSOAs and spanned 21 towns and cities (approximately 17.2% of England’s population) (S1 Table). Clusters accounted for 17,629 diagnoses (34% of total diagnoses) and ranged from 0.6% (Preston) to 51.9% (London). Although the majority of clusters were adjacent to MSOAs of endemic areas, exceptions were observed around endemic areas in Newcastle-upon-Tyne, Bedford, Leeds, Nottingham, and Derby.

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Fig 2. Gonorrhoea endemic regions and outbreak clusters, England: 2012 & 2013.

Brighton, London, Birmingham and Manchester were endemic for gonorrhoea by persistently arising in clusters every six months for two years. The London area is enlarged to the top right to better illustrate endemic areas and clusters. Circles denote 33 clusters across 21 aggregate regions (1,137 MSOAs). Numbers next to clusters correspond to region names listed in S1 Table. All outbreak clusters are interpreted as significant at p<0.05. Age, gender, ethnicity, and IMD were included covariates.

https://doi.org/10.1371/journal.pone.0195178.g002

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Table 2. Characteristics of endemic areas and clusters for gonorrhoea, England: 2012 and 2013.

https://doi.org/10.1371/journal.pone.0195178.t002

The average age (year) of females, heterosexual males, and MSM was 24.4, 28.4, and 32.7, respectively, across the 4 endemic areas and 23.4, 27.6 and 32.4 across the 33 clusters. The proportion of gonorrhoea diagnoses due to PN was similar between individuals with HIV (15.6%) and without HIV (16.5%). Diagnoses seen in heterosexual males and females were similar across clusters (0.7% difference, p = 0.84). Among females, the proportion of PN positive diagnoses ranged from 1.4% (Liverpool) to 47.9% (Bedford) and from 0% (Bradford) to 61% (Bedford) in heterosexual males (Table 2). Heterosexual males accounted for the highest proportion of all diagnoses in Derby and Walsall/Sandwell (both 42%). There was no observable statistical difference or pattern in the proportions of PN diagnoses between heterosexual males and females after controlling for age, gender, ethnicity, and IMD rank. Some areas were dominated by heterosexually acquired infections (Northumberland), others by diagnoses seen in MSM (Brighton). In Brighton and London, diagnoses seen in MSM accounted for over 85% and 65% of all diagnoses, respectively.

Discussion

Spatial-temporal variation is a critical feature of the gonorrhoea epidemic in England. The majority of gonorrhoea diagnoses were observed in urban areas [25], particularly London, Brighton, Manchester, and Birmingham. Although the endemic areas generally corresponded to locations with higher MSM populations (London, Manchester and Brighton), clusters were relatively common among sexual networks of both MSM and heterosexuals [21]. Both endemic areas and clusters overlapped with some of the most deprived areas of England (Liverpool, Manchester, Blackpool, Birmingham, Bradford and the London Borough of Hackney) [26]. Whilst more males presented as index cases to clinical services, a greater proportion of partner notified attendees were female. The value of PN as a case detection strategy was observed in the high proportion of gonorrhoea cases detected using this method; however, this varied considerably with respect to location, sexual orientation, and gender [13,14].

The MSOA analysis highlighted clusters that would otherwise have remained undetected at the LA level. SaTScan analysis is advantageous since it does not require an a priori hypothesis about cluster location, size or duration. The software adjusts for multiple testing and inhomogeneous population density. Additionally, since the technique is not dependent upon administrative unit denominators, the analysis was not influenced by the modifiable areal unit problem [27]. Although GUMCAD captures most gonorrhoea testing and diagnostic activity, including index cases (patients diagnosed first at GUM clinics) and their partners, these cannot be directly linked within the dataset [15,27,28]. Consequently, only the analysis of relative proportions of partner-notified to index based diagnoses can be explored. Whilst this captures current PN practices, interpretation is limited. Furthermore, when the study was conducted only 2012 and 2013 GUMCAD data was available. Although these results accurately describe the recent landscape of gonorrhoea diagnoses and PN across England, they can only approximate the current status due to possible changes in clinic locations, administrative boundaries, and underlying demographics. The new version of GUMCAD (currently under development) will capture more detailed PN information [29]. Recent studies have demonstrated the ability to predict gonorrhoea prevalence, including the development of online tools that predict gonorrhoea prevalence for non-GUM clinics [30,31].

High rates of gonorrhoea are typically distributed within core groups in densely populated urban areas [32]. These endemic areas act as reservoirs that seed clusters into bordering regions. This population structure is characteristic of a meta-population; gonorrhoea endemic populations sustain the epidemic and seed sexual networks in smaller satellite communities through bridging populations [3335]. Infection cycles are relatively independent but a cluster is more likely to become extinct in smaller populations [36].

Identifying endemic areas and clusters and exploring the characteristics of local epidemics is an essential aspect of developing effective control strategies [8]. Four clusters (Northumberland, Liverpool, Bristol and Leeds) found in this analysis were the subject of investigations undertaken by local outbreak control teams [6,8]. Although not all investigations were published because of the need to protect patient confidentiality, those that were illustrate cluster diversity. The outbreak in a socially deprived area of Northumberland was concerned mainly with young heterosexual adults, predominantly young females [6]. The three year investigation detected 360 cases of gonorrhoea within a locally discrete population. An outbreak of high level azithromycin resistant gonorrhoea emerged amongst young heterosexuals (<20) in Leeds at the end of 2014. Subsequent infections were predominantly seen in MSM aged 18 to 31 residing in London and the South East [37].

PN is a key intervention strategy that is most effective when the time between notification and treatment is minimized [13]. However, the proportion of patients attending clinics as a partner of an index case was highly variable. Specialized sexual health services are invariably located in urban areas. Several clusters seen in this analysis were either outside urban areas or did not border endemic areas [14,38]. Ensuring rural populations have access to care could increase PN rates.

Over the past two decades the epidemiology of gonorrhoea has changed significantly, influenced by population flow, sero-adaptive behaviour among HIV-positive MSM, antimicrobial resistance, advances in diagnostic techniques and therapeutic agents, chemsex, and location-based sexual networking applications [21,39]. As a result, the structure of sexual networks is being transformed from a density-dependent factor into a density-independent factor, thereby increasing the potential for infection transmission. Such developments make control increasingly challenging, particularly in locations where infection is endemic. However, whilst social media and geospatial applications are a constantly evolving forum allowing users to share information from discussing sex and locating sex partners, they are also used to interact with health services, promotion campaigns and testing services. Global mass communication provides an opportunity to explore conversations and factors that influence people’s awareness to sexual health and interaction with clinical services in ways that were not previously possible.

Conclusions

Heterogeneity across the gonorrhoea epidemic emphasises the importance of local space-time analyses to plan and evaluate sexual health services as a starting point for public health investigation, hypothesis generation, and research. The future challenge is adapting these analytical and visualisation techniques to create an evidence base that enables healthcare professionals to respond to changes within the developing epidemic.

Supporting information

S1 Text. SaTScan parameters for spatial-temporal identification of gonorrhoea clusters.

https://doi.org/10.1371/journal.pone.0195178.s001

(PDF)

S1 Fig. Rate of gonorrhoea diagnoses, England: 2012 & 2013.

Regions are separated by local authority (LA). Regions are compared to the English average (100.8 diagnoses per 100,000; 95% CI: 100.0, 101.7) as higher, similar or lower. Similar regions were denoted as those within 20% above or below the English average (100–119 and 80–99 diagnoses per 100,000 people, respectively).

https://doi.org/10.1371/journal.pone.0195178.s002

(TIF)

S2 Fig. Gonorrhoea diagnosis rate by gender, England: 2012 & 2013.

Regions are grouped by LA. Regions are compared to the English average (100.8 diagnoses per 100,000; 95% CI: 100.0, 101.7) as higher, similar or lower. Similar regions were denoted as 20% above or below the English average (100–119 and 80–99 diagnoses per 100,000 people, respectively).

https://doi.org/10.1371/journal.pone.0195178.s003

(TIF)

S3 Fig. Quarterly gonorrhoea diagnosis rate with regions grouped by middle-layer super output area (MSOA), England: 2013.

Regions are compared to the English average (12.6/100,000 people) as higher, similar or lower. Similar regions were denoted as those within 20% above or below the English average (12.6–15.1 and 10.1–12.6/100,000 people, respectively).

https://doi.org/10.1371/journal.pone.0195178.s004

(TIF)

S4 Fig. Proportion of partner notified gonorrhoea diagnoses by LA contributing to total gonorrhoea diagnoses for males or females.

Regions are compared to overall English average proportion of positive partner associated gonorrheoa diagnoses (14.5%, 95% CI: 14.2%, 14.8%) spread evenly across all 326 LAs (0.045% expected per LA). Similar regions were denoted as those within 20% above or below the average per LA (0.036%-0.045% and 0.045%-0.053% partner related diagnoses for a given gender).

https://doi.org/10.1371/journal.pone.0195178.s005

(TIF)

S1 Table. Identified gonorrhoea endemic regions and clusters with their participating MSOAs, England: 2012 & 2013.

Endemic regions were chosen by locations that were participating in a high rate cluster every six months. Outbreak clusters were selected based on a statstical level of p<0.05. The cluster numbers correspond to the clusters in Fig 2.

https://doi.org/10.1371/journal.pone.0195178.s006

(DOCX)

Acknowledgments

I would like to extend my gratitude to PHE and all the staff of the STI and HIV teams for their guidance and providing me the dataset for this project. I appreciate their provision of workspace, computers and being, in general, part of the STI team. I would like to thank the GUMCAD team at PHE for orientating me with the provided dataset and all of its background to coding and collection, including Katy Town and Hamish Mohammed for their comments on the draft manuscript. I also appreciate the insight from Dr. Jakob Petersen and his expertise and methods using SaTScan. Chris Grundy has my thanks for following my project progress and offering his suggestions and expertise. Furthermore, I would like to extend my thanks to Sara Haine and my family for their valuable insight and motivation.

References

  1. 1. Sexually Transmitted Infections and Chlamydia Screening in England, 2016 [Internet]. Public Health England; 2017. Available: https://www.gov.uk/government/uploads/system/uploads/attachment_data/file/617025/Health_Protection_Report_STIs_NCSP_2017.pdf
  2. 2. Sexually transmitted infections (STIs): annual data tables—GOV.UK [Internet]. [cited 24 Jun 2017]. Available: https://www.gov.uk/government/statistics/sexually-transmitted-infections-stis-annual-data-tables
  3. 3. Hughes G, Field N. The epidemiology of sexually transmitted infections in the UK: impact of behavior, services and interventions. Future Microbiol. 2015;10: 35–51. pmid:25598336
  4. 4. Health Protection Report: Sexually transmitted infections and chlamydia screening in England, 2013 [Internet]. Public Health England; 2014. Available: http://www.hpa.org.uk/hpr/archives/2014/hpr2414_AA_stis.pdf
  5. 5. Furegato M, Chen Y, Mohammed H, Mercer CH, Savage EJ, Hughes G. Examining the role of socioeconomic deprivation in ethnic differences in sexually transmitted infection diagnosis rates in England: evidence from surveillance data. Epidemiol Infect. 2016;144: 3253–3262. pmid:27511704
  6. 6. Foster K, Cole M, Hotonu O, Stonebridge J, Hughes G, Simms I, et al. How to do it: lessons identified from investigating and trying to control an outbreak of gonorrhoea in young heterosexual adults. Sex Transm Infect. 2016; pmid:26936653
  7. 7. Chen MI, Ghani AC, Edmunds J. Mind the gap: the role of time between sex with two consecutive partners on the transmission dynamics of gonorrhea. Sex Transm Dis. 2008;35: 435–444. pmid:18446084
  8. 8. Chisholm SA, Wilson J, Alexander S, Tripodo F, Al-Shahib A, Schaefer U, et al. An outbreak of high-level azithromycin resistant Neisseria gonorrhoeae in England. Sex Transm Infect. 2015; pmid:26601852
  9. 9. Centers for Disease Control and Prevention (CDC). CDC Grand Rounds: the growing threat of multidrug-resistant gonorrhea. MMWR Morb Mortal Wkly Rep. 2013;62: 103–106. pmid:23407126
  10. 10. Town K, Obi C, Quaye N, Chisholm S, Hughes G. Drifting towards ceftriaxone treatment failure in gonorrhoea: risk factor analysis of data from the Gonococcal Resistance to Antimicrobials Surveillance Programme in England and Wales. Sex Transm Infect. 2017;93: 39–45. pmid:27382010
  11. 11. Ison CA, Town K, Obi C, Chisholm S, Hughes G, Livermore DM, et al. Decreased susceptibility to cephalosporins among gonococci: data from the Gonococcal Resistance to Antimicrobials Surveillance Programme (GRASP) in England and Wales, 2007–2011. The Lancet Infectious Diseases. 2013;13: 762–768. pmid:23764300
  12. 12. Wi T, Lahra MM, Ndowa F, Bala M, Dillon J-AR, Ramon-Pardo P, et al. Antimicrobial resistance in Neisseria gonorrhoeae: Global surveillance and a call for international collaborative action. PLOS Medicine. 2017;14: e1002344. pmid:28686231
  13. 13. Estcourt C, Sutcliffe L. Moving partner notification into the mainstream of routine sexual health care. Sex Transm Infect. 2007;83: 169–172. pmid:17435054
  14. 14. Mercer CH, Aicken CRH, Estcourt CS, Keane F, Brook G, Rait G, et al. Building the bypass—implications of improved access to sexual healthcare: evidence from surveys of patients attending contrasting genitourinary medicine clinics across England in 2004/2005 and 2009. Sex Transm Infect. 2012;88: 9–15. pmid:22199133
  15. 15. Health Protection Agency. Genitourinary Medicine Clinic Activity Dataset (GUMCADv2) [Internet]. [cited 4 Aug 2014]. Available: http://www.hpa.org.uk/Topics/InfectiousDiseases/InfectionsAZ/SexualHealth/SexualHealthProgramme/hivsti_sexhealth_GUMCAD/
  16. 16. Public Health England. GUMCADv2 Guidance to Clinic Staff. 2013.
  17. 17. Office for National Statistics [Internet]. [cited 29 Jul 2014]. Available: https://geoportal.statistics.gov.uk/geoportal/catalog/content/filelist.page
  18. 18. Census 2011 Ethnic group by sex by age—Nomis [Internet]. [cited 29 Jul 2014]. Available: https://www.nomisweb.co.uk/census/2011/dc2101ew
  19. 19. English indices of deprivation 2010—Publications—GOV.UK [Internet]. [cited 29 Jul 2014]. Available: https://www.gov.uk/government/statistics/english-indices-of-deprivation-2010
  20. 20. Public Health Profiles [Internet]. [cited 29 Jul 2014]. Available: http://fingertips.phe.org.uk/profile/sexualhealth/data
  21. 21. Petersen J, Gibin M, Sile B, Simms I. Identifying and interpreting spatiotemporal variation in diagnoses of infectious syphilis among men, England: 2009 to 2013. Sex Transm Infect. 2016; sextrans-2015-052306. pmid:27147614
  22. 22. Kulldorff M. A spatial scan statistic. Communications in Statistics—Theory and Methods. 1997;26: 1481–1496.
  23. 23. Kulldorff M, Information Management Service Inc. SaTScanTM v9.2: Software for the spatial and space-time scan statistics. [Internet]. 2014. Available: www.satscan.org
  24. 24. StataCorp. Stata Statistical Software: Release 13. College Station, TX: StataCorp LP; 2013.
  25. 25. Gesink DC, Sullivan AB, Norwood TA, Serre ML, Miller WC. Does core area theory apply to sexually transmitted diseases in rural environments? Sex Transm Dis. 2013;40: 32–40. pmid:23254115
  26. 26. Communities and Local Government. The English Indices of Deprivation 2010: Statistical Release [Internet]. Government of United Kingdom; 2011. Available: https://www.gov.uk/government/uploads/system/uploads/attachment_data/file/6871/1871208.pdf
  27. 27. Simms I, Gibin M, Petersen J. Location, location, location: what can geographic information science (GIS) offer sexual health research? Sex Transm Infect. 2014; sextrans-2014-051695. pmid:24912479
  28. 28. Geanuracos CG, Cunningham SD, Weiss G, Forte D, Henry Reid LM, Ellen JM. Use of Geographic Information Systems for Planning HIV Prevention Interventions for High-Risk Youths. Am J Public Health. 2007;97: 1974–1981. pmid:17901452
  29. 29. Genitourinary medicine clinic activity dataset (GUMCADv3) pilot—Detailed guidance—GOV.UK [Internet]. [cited 11 Jul 2016]. Available: https://www.gov.uk/guidance/genitourinary-medicine-clinic-activity-dataset-gumcadv3-pilot
  30. 30. Town K, Furegato M, Field N, Hughes G. Estimating gonorrhoea prevalence in young heterosexual men and women attending community-based sexual health services to inform decisions on gonorrhoea testing. Epidemiology & Infection. 2017;145: 1682–1687. pmid:28253939
  31. 31. Guidance for the detection of gonorrhoea in England—GOV.UK [Internet]. [cited 10 Oct 2017]. Available: https://www.gov.uk/government/publications/guidance-for-the-detection-of-gonorrhoea-in-england
  32. 32. Schleihauf E, Watkins RE, Plant AJ. Heterogeneity in the spatial distribution of bacterial sexually transmitted infections. Sex Transm Infect. 2009;85: 45–49. pmid:18723583
  33. 33. Rothenberg R. Maintenance of endemicity in urban environments: a hypothesis linking risk, network structure and geography. Sex Transm Infect. 2007;83: 10–15. pmid:17283360
  34. 34. Jebbari H, Simms I, Conti S, Marongiu A, Hughes G, Ward H, et al. Variations in the epidemiology of primary, secondary and early latent syphilis, England and Wales: 1999 to 2008. Sexually Transmitted Infections. 2011;87: 191–8. http://dx.doi.org/10.1136/sti.2009.040139 pmid:21262786
  35. 35. Le Polain De Waroux O, Harris RJ, Hughes G, Crook PD. The epidemiology of gonorrhoea in London: a Bayesian spatial modelling approach. Epidemiol Infect. 2014;142: 211–220. pmid:23561246
  36. 36. Blanchard JF, Aral SO. Emergent properties and structural patterns in sexually transmitted infection and HIV research. Sex Transm Infect. 2010;86 Suppl 3: iii4–9. pmid:21098056
  37. 37. High level azithromycin resistant gonorrhoea in England—GOV.UK [Internet]. [cited 9 Jul 2017]. Available: https://www.gov.uk/government/publications/high-level-azithromycin-resistant-gonorrhoea-in-england
  38. 38. Aicken CR, Cassell JA, Estcourt CS, Keane F, Brook G, Rait G, et al. Rationale and development of a survey tool for describing and auditing the composition of, and flows between, specialist and community clinical services for sexually transmitted infections. BMC Health Services Research. 2011;11: 30. pmid:21306604
  39. 39. Gilbart VL, Simms I, Jenkins C, Furegato M, Gobin M, Oliver I, et al. Sex, drugs and smart phone applications: findings from semistructured interviews with men who have sex with men diagnosed with Shigella flexneri 3a in England and Wales. Sex Transm Infect. 2015;91: 598–602. pmid:25921020