*Corresponding Author : : Ravi Patel
Department of Trauma and Orthopaedics, Hull
Royal Infirmary, HU3 2JZ, Hull, United Kingdom.
Email: [email protected]
Received : Jun 15, 2022
Accepted : Jul 29, 2022
Published : Aug 05, 2022
Archived : www.jcimcr.org
Copyright : © Patel R (2022).
Sexually transmitted infections (STIs) cause significant morbidity [1], and rates are increasing across the North West [2]. Partner notification (PN) is a public health mainstay in the United Kingdom (UK) for preventing the spread of STIs [3]. However, health services face several challenges when trying to implement PN.
Firstly, while several PN strategies are employed throughout the UK, it is unclear which is most effective, and there are advantages and disadvantages to each [1]. Secondly, there are patient-specific barriers to successful PN [4], and furthermore, there may be service- or clinician-specific barriers to PN [5]. Lastly, PN may involve disclosing confidential information [3], which introduces an ethical challenge.
The primary objective of the review was to identify current challenges to PN applicable to the UK.
Secondary objectives were to describe PN audit data, and to describe UK legal and professional frameworks for patient confidentiality.
Patient-led referrals under PN are more effective when supported by clinician guidance and resources, including leaflets [1]. Furthermore, this practice is recommended under NICE guidance [6]. Therefore, the overarching goal of the project was to produce an information leaflet on PN for patients with STIs.
This aims to fulfil the needs of patients with STIs in two ways:
• Directly, clarifying the PN process, addressing common concerns, and providing the information needed to encourage effective patient referral, and
• Indirectly, providing healthcare professionals a resource to help explain PN during consultation.
The intention of introducing such a leaflet into practice would be to increase successful PN referrals, and by extension, reduce STI transmission.
To find national audit data and guidelines, the Public Health England (PHE), National Institute for Health and Care Excellence (NICE), and British Association for Sexual Health and HIV (BASSH) websites were searched in addition to the primary literature review.
The literature search was performed through the EMBASE and PubMed databases. Search terms combined the concept of sexual health (“sexual health” or “sexual history” or “sexually transmitted infection” or “sexually transmitted disease” or “STI” or “STD”) and partner notification (“partner notification” or “contact tracing” or “confidentiality”).
Articles were constrained to books and documents, clinical studies, meta-analyses, systematic reviews, and reviews.
Specific dates were not defined, as information on the history of partner notification was sought.
No exclusion criteria were defined.
Contact tracing is a process which identifies individuals who have been in contact with a person known to have a transmissible disease [1].
For STIs, contact tracing aims to inform current and past sexual partners of the index case that they are at risk of infection, a process known as “partner notification” (PN) [3].
STIs are often asymptomatic [7] but may still be transmissible and can lead to serious complications [8]. Therefore, PN aims to test and treat asymptomatic individuals to reduce infection sequalae, prevent re-infection of the original patient, and prevent further spread [8].
Various strategies have been employed in facilitating PN (Table 1).
Strategy | Description |
---|---|
Simple patient referral | The patient is encouraged to notify relevant sexual partners. |
Enhanced patient referral | As patient referral, with resources and/or counselling provided to facilitate explanation (e.g. information leaflets). |
Provider referral | Healthcare professionals notify the partner(s) anonymously. |
Contract referral | The patient is encouraged to notify their partner(s). If the partner does not attend an appointment within a specified timeframe, they will be contacted anonymously by healthcare professionals. |
Expedited partner therapy | The patient offers treatment (e.g. a prescription) to their partner(s) without a medical consultation (N.B. this strategy was developed in the United States is not legal in the UK). |
Evaluating the efficacy of PN empirically would require monitoring asymptomatic individuals exposed to STIs, which is not ethically feasible. However, dynamic modelling simulations suggest that PN accounts for some reduction in the UK population prevalence of chlamydia and gonorrhoea infection [9].
Concerning different PN methods, a 2013 Cochrane systematic review of randomised controlled trials and a 2014 health technology assessment analysis drew similar conclusions [1,9]. There was moderate-quality evidence that expedited partner therapy decreases index case reinfection compared to simple patient referral [1]. However, it was not superior to enhanced patient referral [1]. Overall, the difference in rate of adverse effects between patient, provider, and contract referral methods was not statistically significant [1].
Separately, in a 2016 review of systematic reviews, it was concluded that patient counselling is important for enhanced patient referral, while there was no evidence to support didactic consultation [10].
Globally, barriers to PN are similar [4,11,12]. A 2010 systematic review on PN in developing countries found that for current partners, these include:
• embarrassment or stigma attached to an STI,
• fear of loss of respect,
• fear of rejection or divorce [4].
For casual partners, major barriers included being non-contactable and perceived lack of benefit [4].
A survey of 776 sexual health patients in South Africa drew similar conclusions, but additionally found that fear of a violent reaction was an important barrier for both men and women [11].
In a United States study from 2000, 79 people with STIs were interviewed about PN. Barriers included fear of gossip, rejection, or abuse, or the perception that the STI had been knowingly transmitted to them [12].
More broadly, a 2020 systematic review analysed barriers to engagement with contact tracing services (13). Barriers were categorised into five themes: concerns around privacy, mistrust, lack of support or information, worry of stigmatisation, and contact tracing system-specific challenges (13).
No studies on barriers to PN were found in the UK population.
In their 2007 recommendations, NICE advise that: “All (primary care) services should include arrangements for the notification, testing, treatment, and follow-up of partners of people who have an STI (partner notification)” [14]. Additionally, patient referral is encouraged as an initial strategy [14]. In a 2019 NICE quality standard, it is added that:
• commissioners should arrange PN services provision,
• service providers should establish pathways for PN, offering PN discussion, and specialist referral,
• healthcare professionals should understand local PN procedures and support their patients in this process (6).
Nationally, procedural standards are set by BASHH [3].
This guidance lists infections requiring PN, and for patients with these infections, either a PN discussion or a reason for PN refusal should be documented (3). This discussion should clarify which partners will be notified and the method of notification (3).
Patient, partner, and contract referral are all acceptable in the UK (3), although patient referral is the most common (15). The method employed depends on local service provision and individual patient factors (3, 8). For example, provider referrals are generally carried out by sexual health advisers (15), as this process requires specific and documented competencies (3, 8).
PN is not necessary if a partner has already attended a consultation for the relevant infection, is considered untraceable due to inadequate information, or if it would put patient wellbeing at risk (3).
In England, PN in 18–24-year-olds with chlamydia infection is audited against BASHH standards by Public Health England [5, 16]. The most recent report, published in 2020, examines data between 11th September and 23rd October 2019, covering 52% of upper tier local authorities [5].
In total, 93% of patients had a documented PN offer compared to the standard of 97%, which was a decrease from 94% in 2017 [5]. Rates varied between services, although general practice (GP) and genitourinary medicine (GUM) both offered PN in only 87% of cases (Figure 1) [5].
The commonest reasons for not offering PN were:
*Sexual and Reproductive/Contraception and Sexual Health services Information sourced from [5].
• “No documented evidence” (43%),
• “Other” (19%),
• No reason given (15%),
• “Lost to follow-up” (13%).
Less common reasons were patients attending other services, transferring care, or undertaking PN elsewhere.
In the UK, patients with STIs are not legally obliged to notify their partners [8] and may not wish information to be shared between healthcare services [3]. However, these are prerequisites for successful PN, which raises the ethical challenge of sharing confidential information [8].
Confidentiality in medicine is governed by several laws, including common law, data protection law, and the Human Rights Act 1998 [17]. Legal confidentiality frameworks vary across different countries in the UK [17].
Concerning STIs, the NHS Trusts and Primary Care Trusts Directions 2000 (Sexually Transmitted Diseases) regulates practice in England [17]. This states that information identifying a patient with an STI may be disclosed to a treating medical professional or to prevent spread of disease [17].
These legal frameworks inform the General Medical Council (GMC) guidelines on confidentiality for doctors [17,18]. Paragraph 9 states that confidential information can be disclosed if either:
i) the patient consents,
ii) disclosure is in the best interests of someone who lacks capacity,
iii) disclosure is required or approved by a legal framework, or
iv) disclosure is justifiable for the public interest (17).
Undertaking PN without patient consent falls under public interest disclosure (18).
The GMC additionally offer guidance on disclosing information about serious communicable diseases (18). A serious communicable disease is defined as: “any disease that can be transmitted from human to human and that can result in death or serious illness. It particularly applies to, but is not limited to, HIV, tuberculosis, and hepatitis B and C” (18).
Paragraphs 12-15 advise that:
• Patients should be told how they can protect others from infection (18).
• Close contacts of a patient with a serious communicable disease may be informed if:
o there is a risk of infection likely to cause serious harm, and
o the patient will not inform them (18).
• If an adult at risk of serious harm from infection lacks the capacity to understand this information, this should be disclosed to an appropriate responsible person or authority (18).
• If practicable, the patient should be told before disclosing information and their identity should not be disclosed (18).