Objectives Malignant melanoma has high morbidity and mortality rates. Early diagnosis improves prognosis. Clinical prediction rules (CPRs) can be used to stratify patients with symptoms of suspected malignant melanoma to improve early diagnosis. We conducted a systematic review of CPRs for melanoma diagnosis in ambulatory care.
Design Systematic review.
Data sources A comprehensive search of PubMed, EMBASE, PROSPERO, CINAHL, the Cochrane Library and SCOPUS was conducted in May 2015, using combinations of keywords and medical subject headings (MeSH) terms.
Study selection and data extraction Studies deriving and validating, validating or assessing the impact of a CPR for predicting melanoma diagnosis in ambulatory care were included. Data extraction and methodological quality assessment were guided by the CHARMS checklist.
Results From 16 334 studies reviewed, 51 were included, validating the performance of 24 unique CPRs. Three impact analysis studies were identified. Five studies were set in primary care. The most commonly evaluated CPRs were the ABCD, more than one or uneven distribution of Colour, or a large (greater than 6 mm) Diameter (ABCD) dermoscopy rule (at a cut-point of >4.75; 8 studies; pooled sensitivity 0.85, 95% CI 0.73 to 0.93, specificity 0.72, 95% CI 0.65 to 0.78) and the 7-point dermoscopy checklist (at a cut-point of ≥1 recommending ruling in melanoma; 11 studies; pooled sensitivity 0.77, 95% CI 0.61 to 0.88, specificity 0.80, 95% CI 0.59 to 0.92). The methodological quality of studies varied.
Conclusions At their recommended cut-points, the ABCD dermoscopy rule is more useful for ruling out melanoma than the 7-point dermoscopy checklist. A focus on impact analysis will help translate melanoma risk prediction rules into useful tools for clinical practice.
- PRIMARY CARE
- Clinical prediction rules
- Systematic review
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Strengths and limitations of this study
The main strengths of this review are the use of broad inclusion criteria, the systematic search of multiple databases not limited by language, use of the CHARMS checklist to assess methodological quality, pooling data from a broad range of studies to enhance generalisability and the use of a broad definition of primary care to account for the variation in primary care services and access internationally. Quality assessment criteria were used to assess risk of bias and the majority of studies were at low risk in relation to the randomisation procedure and monitoring of loss to follow-up.
A large proportion of studies did not provide sufficient information and data to perform stratified meta-analysis according to different levels of risk.
Current research shows that dermoscopic clinical prediction rules (CPRs) may be a useful tool for primary care physicians prioritising appropriate referrals for higher risk patients and adopting a watchful waiting strategy in lower risk patients but future impact analysis research is necessary to establish their impact on patient outcomes.
The incidence of malignant melanoma in most developed countries has been steadily rising (faster than other cancer types) in recent decades.1 ,2 Increases in the age-standardised incidence of at least 4–6% per annum have been reported internationally in many fair-skinned populations including Australia, the USA and most of Europe.3–5 Simultaneously, there has been a significant rise in overall 5-year survival in melanoma patients, largely attributable to earlier detection and diagnosis of thinner tumours.6 While the majority of patients may survive melanoma, the disease has a significant impact on patient quality of life7 and healthcare expenditure, with the average annual total treatment costs for melanoma in the USA increasing to US$3.3 billion in 2011.8 Melanoma is potentially preventable since a significant risk factor, exposure to ultraviolet (UV) radiation, is modifiable.9 However, other risk factors (eg, number naevi, eye and hair colour, freckles, familial history and genetic predisposition) also play an important role in the risk of developing melanoma.10 ,11
Early detection followed by curative surgery greatly improves melanoma prognosis. However, early detection may be affected by the challenging natures of differential diagnosis of pigmented lesions. Particularly in primary care where the evaluation of suspected skin lesions is imposing an increasing burden due to rising incidences of skin cancer.12 It has been suggested that primary care practitioners' skills of diagnosing skin lesions could be improved.13 A number of clinical prediction pules (CPRs) and computer-assisted diagnostic tools have been developed to assist in distinguishing malignant melanoma from benign pigmented skin lesions. The UK National Institute for Clinical Excellence (NICE) guidelines advise against routine use of computer-assisted diagnostic tools in the initial evaluation of a pigmented skin lesion (NICE guidelines) and promote use of the weighted 7-point checklist in primary care to guide referral (NG12). When used by dermatologists for the diagnosis of melanoma, certain CPRs have demonstrated high sensitivity and specificity.6 Although each CPR has its own unique elements, there is significant overlap in terms of their content (see online supplementary appendix 1), and while their use is promoted, it is unclear which rules are most suitable for use in primary care.
CPRs may be for use in clinical (ie, naked eye) examination, or in conjunction with dermoscopy. Dermoscopy, dermatoscopy or epiluminescent microscopy refers to the examination of pigmented skin lesions using surface microscopy.14 ,15 The use of dermoscopy, primarily by dermatologists, has been found to increase diagnostic accuracy compared with naked-eye inspection, as it allows the visualisation of features that are not visible to the naked eye.14–16 However, the effectiveness of dermoscopy depends on clinical experience and training. Dermatologists with formal training in dermoscopy have higher melanoma detection rates compared with untrained dermatologists and primary care physicians.16–18
As primary care or ambulatory care physicians are frequently and increasingly confronted with the care of skin lesions suspected of malignancy,12 it is essential to identify tools to aid primary care practitioners to differentiate patients with clinically significant lesions, requiring referral, from those who can be treated and monitored in primary care. The aim of this study was to perform a systematic review of CPRs for the diagnosis of malignant melanoma, to evaluate their diagnostic accuracy in primary care and specialist outpatient settings, among patients with a pigmented skin lesion. Secondary aims were to review studies that have examined the implementation of CPRs in clinical practice through impact analysis studies.
The protocol for this systematic review was published on PROSPERO (CRD42015020898) and was conducted according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.19
Search strategy and data sources
A systematic literature search was conducted (May 2015) including the following databases: PubMed, EMBASE, PROSPERO, CINAHL, the Cochrane Library and SCOPUS, using combinations of the following keywords and MeSH terms: melanoma/diagnosis, melanoma, prediction, score, model, decision, sensitivity, specificity, validate, derived. Hand searches of references of retrieved full-text articles and key author searches supplemented the search. No date or language limits were imposed.
All articles were initially screened for inclusion according to title and abstract by two reviewers (NW, EH). Full-text articles of studies considered eligible for inclusion were independently read by both reviewers, with any disagreements resolved by a third reviewer (BC).
Validation studies were eligible for inclusion if they met the following criteria;
Population: Adults (age ≥18 years) with a pigmented skin lesion in ambulatory care settings in general practice/family medicine, dermatology, plastic surgery and other relevant specialties.
Risk: Derivation and/or validation of a CPR for melanoma diagnosis to aid decision making about referral or investigation of a pigmented skin lesion. CPRs were defined as ‘a clinical tool that quantifies the individual contributions that various components of the history, physical examination and investigations make toward the diagnosis, prognosis or likely response to treatment in a patient’.
Comparison: Usual clinical judgement for decision making about referral or investigation OR another CPR for melanoma diagnosis.
Primary outcome: Performance of a CPR for predicting diagnosis of malignant melanoma (in terms of sensitivity, specificity, negative predictive values and positive predictive values).
Observational study designs (eg, cohort, cross-sectional, case–control) were included. Studies were excluded where they had undergone derivation only, reported individual predictors only, or used computer-assisted diagnostic tools, following the NICE guideline recommendation against the routine use of computer-assisted diagnostic tools.20
The following study designs were included for impact analysis: (cluster) randomised controlled trials (RCTs), controlled before–after studies or interrupted time series studies. We excluded uncontrolled study designs. We included studies where a melanoma CPR was used to predict melanoma compared with usual care in the clinical setting. The outcomes of interest included physician behaviour, process of care, patient outcomes and/or cost-effectiveness. A requirement for inclusion was that the CPR comprised the entire intervention. Studies where the CPR was implemented as part of a broader guideline, protocol or decision aid were excluded. Studies that used a CPR to determine eligibility for trial inclusion but were not part of the intervention were also excluded.
Data were extracted by four reviewers (LA, HB, HS, EH) using a data form based on the CHARMS checklist.21 Data extracted included study design and setting, patient demographics and inclusion criteria, CPR name, CPR type (clinical or dermoscopic), predictive accuracy of the CPR (sensitivity/specificity) and for impact analysis, the impact on the primary outcome.
Critical appraisal of studies
Two reviewers (EH, NW) critically appraised included studies using the CHARMS checklist, developed to provide guidance on data extraction and critical appraisal of prediction modelling studies.21 The checklist contains 11 domains of critical appraisal. The methodological quality of each study was independently evaluated by two reviewers and by a third reviewer if consensus was not reached. The methodological quality of each impact analysis study was also independently assessed, using an appropriate quality assessment checklist. RCTs were assessed using the Cochrane risk of bias tool and controlled before–after studies were evaluated using Cochrane criteria for these study designs.22
Statistical analysis was conducted using Stata V.12 (StataCorp, College Station, Texas, USA), in particular the metandi and midas commands. For each CPR, a standard cut-point was identified (table 1). From each included study we extracted (where available) the numbers of true positives, false positives, true negatives, false negatives, sensitivity and specificity and their corresponding 95% CIs. Where sensitivity/specificity for more than one observer was reported, the mean value was included in the analysis. Studies were grouped for analysis by CPR type (ie, clinical or dermoscopic). Summary estimates of sensitivity and specificity and their corresponding 95% CIs were calculated using the bivariate random effects model (midas). The bivariate model has the benefits of being easily interpretable, is technically straightforward to undertake and takes into account the sample and heterogeneity beyond chance between studies.23
Individual and summary estimates of sensitivity and specificity were plotted on a hierarchical summary receiver operating characteristic (HSROC) graph. This approach incorporates sensitivity and specificity, while taking into account the correlation between the two.24 Sensitivity (true positive) was graphed on the y-axis and 1-specificity (false negative) on the x-axis. The 95% confidence region and the 95% prediction region were also plotted around the pooled estimates in order to depict the precision with which the pooled estimates were determined (confidence ellipse around the mean value) and to illustrate the amount of between-study variation (prediction ellipse).
The search strategy yielded a total of 25 816 articles. Of these 9481 were duplicates and 16 166 were deemed irrelevant based on title/abstract. The remaining 171 were reviewed in full with 51 meeting the inclusion criteria (see online supplementary appendix 2). From these, 24 unique melanoma CPRs were identified (table 1). Twelve papers reported derivation and validation studies, 36 were validation studies only and three were impact analyses.
Summary of studies
Table 2 summarises the characteristics of the included studies. The majority (11, 22%) were conducted in Italy14 ,15 ,25–34 and ranged from an analysis of 40 lesions to 1580 lesions. From 13 studies providing information, mean age of included patients ranged from 36.7 to 53.25 ,28 ,31 ,35–44 From the 14 studies that reported gender, the proportion of males ranged from 22% to 60%.25 ,31 ,33 ,35–45 In total, 31 of the 50 studies were published in/or after 2000.14 ,25 ,28 ,29 ,31–37 ,42–44 ,46–62 Five studies were set in primary care,36 ,44 ,49 ,62 ,63 with the remainder undertaken in specialist outpatient settings.
Summary of CPRs identified
Of the 24 rules identified, four were clinical (ie, naked eye), 17 were dermoscopic and the remaining three used novel diagnostic technologies. The most commonly applied clinical CPR was the ABCDE rule (five studies),6 ,15 ,28 ,64 ,65 while for dermoscopy the most common were the Asymmetry, irregular Borders, more than one or uneven distribution of Colour, or a large (greater than 6 mm) Diameter (ABCD) rule of dermoscopy (23 studies)14 ,25 ,26 ,29 ,31 ,32 ,39 ,42 ,43 ,47–49 ,52 ,53 ,57 ,65–70 and the 7-point checklist for dermoscopy (17 studies).14 ,25 ,26 ,29 ,35 ,37 ,42 ,43 ,46–50 ,52 ,56 ,57 ,59
Each of the elements included in the 24 rules identified are presented in table 3. All four clinical rules included the elements of diameter and colour variegation (table 3 and see online supplementary appendix 1). The most frequently included elements in the 17 dermoscopic rules were multiple colours (13 rules), asymmetry (12 rules) and streaks (10 rules) (table 3 and see online supplementary appendix 1).
Methodological quality of validation studies
Based on the CHARMS checklist, the quality of included studies varied.21 All studies had weaknesses in study design and quality assessment was often hindered by poor reporting of methods. The studies had reasonable sample sizes and all provided adequate definitions of the outcome of interest. However, a number of important weaknesses were identified. None of the studies reported on missing data and key performance measures of model performance (eg, calibration) were often missing. Derivation studies typically reported information on model development, in terms of selection of candidate predictors, selection of predictors during modelling, and model evaluation. However, often the methods applied introduced a strong risk of bias, for example, a number of studies described splitting the original sample into a development and validation sample which is considered statistically inefficient and results in overfitting of the model.21 Full results of the quality assessment are shown in online supplementary appendix 3.
Predictive accuracy of melanoma CPRs
The results for the most commonly applied CPRs, the ABCD rule and the 7-point checklist are presented here. The sensitivity and specificity of all rules identified (including the ABCDE clinical rule, the seven features for melanoma rule and Menzies dermoscopy for melanoma rule) are summarised in table 4.
Clinical (naked eye) CPRs for melanoma diagnosis
Four studies validating the ABCDE clinical rule6 ,15 ,28 ,64 and one validating the ABCD clinical rule65 were included. There was insufficient data to conduct any meta-analysis. Rao et al reported a sensitivity of 0.84 and specificity of 0.78, for an unspecified cut-point.65
Six studies validating the original and revised 7-point checklist were included. There was insufficient data to conduct a meta-analysis. Of the four studies validating the original 7-point checklist (cut-point ≥3), three reported sensitivity (range 0.44–0.86, mean 0.70) and specificity (range 0.62–0.94, mean 0.74).40 ,41 ,44 Only one of the four studies validating the revised 7-point checklist (cut-point ≥1) reported sensitivity (0.92) and specificity (0.33) (table 4).44
Dermoscopic CPRs for melanoma diagnosis
ABCD rule of dermoscopy
The ABCD rule of dermoscopy (also described as the ABCD rule of Stolz), was validated in 23 studies, 15 of which applied a cut-point of >4.75 (indicating a suspicious lesion) and six studies a cut-point of 5.45 (highly suggestive for melanoma). At a cut-point of >4.75, eight studies provided sufficient information for meta-analysis,42 ,43 ,47 ,52 ,65 ,71 resulting in a pooled sensitivity of 0.85 (95% CI 0.73 to 0.93) and specificity of 0.72 (95% CI 0.65 to 0.78) (figure 1A, B). This indicates that at this cut-point, the dermoscopy CPR is more useful for ruling out rather than ruling in melanoma, with a higher pooled sensitivity than specificity. I2 were high (>70%), indicating a high degree of heterogeneity. Of the seven studies excluded from meta-analysis, sensitivity ranged from 0.71 to 0.91 (mean 0.79) and specificity ranged from 0.43 to 0.92 (mean 0.72). None of the six studies that applied a cut-point of 5.45 were suitable for meta-analysis. From four studies that presented the information, sensitivity ranged from 0.73 to 0.98 (mean 0.85) and specificity ranged from 0.46 to 0.91 (mean 0.79) (table 4).
Seven-point checklist for dermoscopy
The 7-point checklist for dermoscopy was validated in 18 studies, 17 of which applied a cut-point of 3. 11 studies provided sufficient information for meta-analysis, revealing a pooled sensitivity of 0.77 (95% CI 0.61 to 0.88) and pooled specificity of 0.80 (95% CI 0.59 to 0.92) (See figure 2A, B).25–27 ,35 ,37 ,42 ,43 ,47 ,50 ,52 ,71 There was a high degree of heterogeneity in the results (I2>90%). Removing two outliers27 ,50 made minimal difference to the pooled result. Only one study validated the revised 7-point checklist for dermoscopy and reported sensitivity 0.78 and specificity 0.65 for a cut-point of 3 (table 4).27
We identified three unique studies that examined the impact of a melanoma CPR on processes of care (melanoma diagnosis and referrals), however, no patient outcomes were examined (table 2).62 ,63 The methodological quality of these studies is presented in online supplementary appendix 4.
Using a controlled before–after design, Westerhoff et al investigated the impact of an educational intervention about the Menzies 1996 rule on melanoma diagnosis by family physicians (FP). The control group did not receive the training. Postintervention, there was a significant improvement in melanoma diagnosis (75.9% vs 62.7%, p<0.001). No significant improvement was seen in the control group (54.8% vs 53.7%, p=0.59).62
Walter et al conducted a RCT to compare the use of a new imaging device, the MoleMate system (SIAscopy with a primary care scoring algorithm), to current best practice (clinical history, naked-eye examination, 7-point checklist). The authors found no difference between these two approaches in terms of appropriate referrals (the proportion of referred lesions that secondary care experts biopsied or monitored) to urgent skin cancer clinics (intervention 56.8% vs control 64.5% p=0.11) or the proportion of benign lesions appropriately managed in primary care (intervention 99.6% vs control 99.2%, p=0.46).63
Argenziano et al's RCT,72 involved primary care physicians first attending a 1-day training course describing the ABCD rule (cut-point unspecified) and the 3-point checklist. They were then randomly assigned to assess patients with skin lesions, either by clinical (ie, naked eye) examination, or by dermoscopy using the 3-point checklist. The referral assessments were checked for accuracy by dermatologists. The dermoscopy arm demonstrated a 25% improvement in the sensitivity of primary care referrals of pigmented lesions compared with the naked-eye examination (79.2% vs 54.1%, p=0.002), without a reduction in specificity (71.8% vs 71.3%, p=0.915).72
Summary of findings
This systematic review identified 48 studies validating a total of 24 CPRs for melanoma. Overall, the majority of validation studies used dermoscopic CPRs, with very few studies validating clinical CPRs. Meta-analysis of the dermoscopic CPRs demonstrated relatively high pooled estimates of sensitivity (0.77–0.86). The clinical implication is that applying dermoscopy CPRs will enable low-risk patients to be observed and kept under review in a primary care setting, without immediate referral for excision to secondary care. Meta-analysis was not possible for clinical CPRs but individual studies report variable sensitivity, ranging from 0.44 to 0.86. Three impact analysis studies were identified, with two reporting an improvement in melanoma diagnosis with the use of a CPR.
Context of previous research
The sensitivities and specificities we report indicate that currently available CPRs are reasonably good at ruling out melanoma. The pooled sensitivity of the ABCD rule for dermoscopy (cut-point of >4.75) was 0.85 (95% CI 0.73 to 0.93), higher than that of the 7-point checklist for dermoscopy (0.77, 95% CI 0.61 to 0.88). While this evidence would support the use of such rules in prioritising appropriate referrals for higher risk patients and adopting a watchful waiting strategy in lower risk patients, there are a number of important caveats that may prevent their adoption in primary care.
Melanoma is a high-stakes condition, one which doctors tend to be cautious in diagnosing, often preferring to excise a benign lesion rather than to miss a potentially fatal cancer.73 In such cases, a CPR with near perfect sensitivity would be desirable, however, it has been argued that a lower sensitivity should not prevent CPR use unless usual decisions, made without the rule, are demonstrably better.74 Our results are comparable with previous systematic reviews focused on melanoma diagnosis across healthcare settings in highlighting that dermoscopic CPRs are demonstrably better in terms of diagnostic accuracy in comparison with inspection by the naked eye.16 ,75 However, even a rule with almost 100% sensitivity may not be adopted. For instance, implementation of the Canadian CT Head Rule, despite 100% sensitivity in validation studies, did not result in a reduction in imaging rates, with clinicians' reporting unease with certain components of the rule and fear of missing a high-stakes diagnosis as reasons for not adopting the CPR.76
Before considering whether to use a CPR in clinical practice, it is essential that its performance be established through external validation (ie, in settings outside where it was derived). We identified a number of external validation studies in this review, however, in keeping with much CPR research, the reporting of these studies was often poor.77 ,78 In particular, the common issues of limited acknowledgement and handling of missing data and key performance measures of prediction models, that is, calibration, being omitted was encountered.77 The lack of available data in some papers meant not all studies could be combined in the meta-analysis, meaning the sensitivities and specificities reported here are not based on the totality of existing evidence. Furthermore, we were unable to assess diagnostic accuracy at different cut-point thresholds for respective CPRs. Improved reporting of CPRs at cut-point thresholds will enable pooling of diagnostic accuracy data, and will provide more robust measures of diagnostic accuracy. After validation, impact analysis studies are undertaken to determine the impact of the implementation of a CPR on processes and outcomes of care. Despite increasing interest in developing and validating CPRs relevant to primary care, relatively few have undergone impact analysis.79 Despite the large number of CPRs identified in this review, we identified only three impact analysis studies, with only two studies reporting an improvement in correct melanoma diagnosis in primary care as a result. Arguably, the dearth of well conducted and clearly reported external validation and impact analysis studies undermines trust in the use of such rules in practice.77
Current NICE guidelines for melanoma detection and management recommend dermoscopy of any suspicious lesion, advising against using computer-assisted diagnostic tools (NG14) while promoting use of the weighted 7-point checklist in primary care to guide referral (NG12).20 Based on the findings of this review, the ABCD rule for dermoscopy had a higher sensitivity than the seven point for dermoscopy checklist at their respective cut-points, indicating its potential for use in primary care. Dermoscopy, however, requires training and equipment, and is less commonly performed in primary care. Evidence suggests that dermatologists have better diagnostic accuracy than primary care physicians.18 Three studies retrieved in our search assessed dermoscopy CPR performance when applied by non-experts, with two studies reporting that the CPRs performed well overall when used by non-experts, mainly primary care physicians.49 ,66 ,72 Westerhoff et al62 and Blum et al80 demonstrated that training primary care physicians to use dermoscopy with CPRs showed significant improvement in the diagnosis of melanoma compared with naked eye inspection. Alongside the use of CPRs, training in dermoscopy would seem to be a strategy that will enhance diagnostic accuracy of melanoma in the future particularly in light of emerging evidence of differences in dermoscopic features of melanoma such as head and neck melanoma.81 It has also been highlighted that significant efforts are needed to standardise and improve dermoscopic terminology to more broadly promote the use of dermoscopy in the primary care setting.82 Of the 24 rules identified in this review, four were clinical (ie, naked eye) and 17 were dermoscopic. Owing to the limited number of studies and available data, no meta-analysis of clinical CPRs could be conducted. The range of reported sensitivities from individual studies indicates that there is insufficient evidence to recommend their use in practice.
Strengths and limitations of our study
The main strengths of this review are the use of broad inclusion criteria, the systematic search of multiple databases not limited by language, use of the CHARMS checklist to assess methodological quality, pooling data from a broad range of studies to enhance generalisability and the use of a broad definition of primary care to account for the variation in primary care services and access internationally. However, the findings of this systematic review need to be interpreted in the context of the limitations of the original studies. The lack of available data in some papers meant not all studies could be combined in the meta-analysis. A number of studies that validated CPRs and algorithms using novel diagnostic technologies which incorporated computerised image analysis and artificial intelligence were excluded from the review as routine use of these are not currently recommended in UK NICE clinical guidelines. Significant heterogeneity existed between the studies with respect to differences in the study populations and application of the CPR. Finally, individual patient data that enables pooling of risk scores at the different cut-points would enable researchers to explore the clinical use of applying risk scores at different cut-points with the purpose of assessing the role of melanoma CPRs at the different diagnostic thresholds of ‘ruling out’ (using highest pooled sensitivity) or ‘ruling in’ (using highest pooled specificity) of respective melanoma CPRs.
Implications for practice and future research
Early detection followed by curative surgery greatly improves the prognosis of malignant melanoma. As the incidence of melanoma skin cancer increases, primary care physicians are increasingly required to screen for melanoma.12 Therefore, efforts to increase the early detection of melanoma must focus on supporting primary care physicians in performing skin cancer screenings with recent evidence highlighting the benefits of developing targeted screening strategies in high-risk patients in primary care.18 ,83 This systematic review identified 24 separate clinical (naked eye) and dermoscopic CPRs, with some overlap in the included the elements. Our analysis highlights that dermoscopic CPRs have reasonable sensitivity, with the ABCD rule for dermoscopy having better sensitivity than the 7-point checklist for dermoscopy. Further development of new rules is unlikely to benefit the field of research. An increased emphasis on better reporting of validation studies, particularly at different cut-point thresholds, would allow for the conduct of more robust diagnostic accuracy meta-analysis to inform decision making. Further methodologically robust RCTs are necessary also to examine the impact of implementing CPRs in clinical practice, in terms of patient outcomes, physician behaviour, processes of care and cost-effectiveness. Finally, while guidelines promote the use of dermoscopy in the assessment of pigmented skin lesions, there needs to be greater emphasis on training in primary care on this examination technique.
This systematic review and meta-analysis shows that dermoscopic CPRs have reasonably high pooled estimates of sensitivity and may be a useful tool for primary care physicians prioritising appropriate referrals for higher risk patients and adopting a watchful waiting strategy in lower risk patients. The ABCD rule of dermoscopy has higher pooled sensitivity than the 7-point checklist for dermoscopy, when consideration about ruling out melanoma is being made. A focus on impact analysis may help translate melanoma CPRs into useful and effective triage tools for use in primary care.
Contributors EH, NW and BC drafted the manuscript. EH, NW and BC contributed to development of the selection criteria, the risk of bias assessment strategy and the data extraction criteria. EH developed the search strategy. HB, LA and HS contributed the data extraction and quality assessments. BC and TF read, provided feedback and approved the final manuscript.
Funding This systematic review is funded by the HRB Centre for Primary Care Research under grant number HRC/2014/1, Royal College of Surgeons in Ireland (RCSI), Dublin, Ireland.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement No additional data are available.
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