Clinical Review

Skin in the game: epidemiology analysis of skin cancer in rural Western Victoria

AUTHORS

name here
Tori Dopheide
1 MD, BBiomedS

name here
Jessica Feeney
2 BSc (ParamedSc), BTrngDev, Medical Student (Y3) *

name here
Joshua Eaton
1 MD, BCOM

name here
Jessica Beattie
3 MHHSM, Lecturer in Rural General Practice (Program Development and Support) ORCID logo

name here
Rizwan Jaipurwala
3 FRACGP, Affiliate Lecturer ORCID logo

name here
Lara Fuller
3 FRACGP, Director of Rural Medical Education and Director Rural Community Clinical School ORCID logo

name here
Leesa Walker
4,5 FRACGP, FRACGP-RG, Senior Lecturer

CORRESPONDENCE

*Ms Jessica Feeney

AFFILIATIONS

1 School of Medicine, Deakin University, Geelong, Vic. 3216, Australia

2 Oceania University of Medicine, Apia, Samoa

3 Rural Community Clinical School, School of Medicine, Deakin University, PO Box 713, Colac, Vic. 3250, Australia

4 Rural Health South Australia, Flinders University, PO Box 3570, Mount Gambier, SA 5290, Australia

5 Present address: Hamilton Medical Group, Foster Street, PO Box 560, Hamilton, Vic. 3300, Australia

PUBLISHED

29 January 2025 Volume 25 Issue 1

HISTORY

RECEIVED: 25 May 2023

REVISED: 4 July 2024

ACCEPTED: 5 November 2024

CITATION

Dopheide T, Feeney J, Eaton J, Beattie J, Jaipurwala R, Fuller L, Walker L.  Skin in the game: epidemiology analysis of skin cancer in rural Western Victoria. Rural and Remote Health 2025; 25: 8471. https://doi.org/10.22605/RRH8471

AUTHOR CONTRIBUTIONSgo to url

This work is licensed under a Creative Commons Attribution 4.0 International Licence


abstract:

Introduction: The aim of this clinical review was to evaluate the number and types of skin cancer excised by GPs in a rural clinic in South West Victoria, Australia, and analyse the number needed to treat (NNT, a common metric for evaluating skin cancer detection) and the influence of clinician experience on diagnostic accuracy.
Methods: This retrospective audit of patient records was for two discrete time periods (14 October 2019 to 5 November 2020 and 1 February 2021 to 17 February 2022). Data extracted included number of lesions removed, location of lesions, skin cancers detected, and patient and clinician characteristics.
Results: A total of 789 lesions were excised; of these, 449 (56.9%) were histologically confirmed to be malignant. Males were statistically more likely to be diagnosed with a malignancy (p≤0.001). The NNTs for melanoma and non-melanoma skin cancers were 5.4 and 1.4, respectively. Experienced GPs (>5 years experience) were better at detecting melanoma and non-melanoma skin cancers than their junior colleagues.
Conclusion: This study investigated the demographic characteristics of rural skin cancer patients and the diagnostic skills of GPs in South West Victoria. Results obtained found males had a higher risk of skin cancer than females. The diagnostic accuracy for all skin cancers improved with clinician experience and a lower overall NNT for both melanoma and non-melanoma skin cancers when compared to existing literature. Differences in this may highlight the experience, exposure, and professional interest of rural GPs, addressing a lack of specialist services in the area.

Keywords:

Australia, diagnostics, health education, lesion, melanoma, non melanoma skin cancer, rural medicine, rural Victoria general practice, self skin checks, skin cancer, skin cancer removal, skin checks.

full article:

Introduction

Skin cancer is a major public health issue in Australia, with the highest incidence of skin cancer globally1. Melanoma in particular is renowned as ‘Australia’s national cancer’1. Non-melanoma skin cancer (NMSC) is the cancer most commonly diagnosed in general practice, both in Australia and globally. NMSC frequency is five times that of all other cancers combined, resulting in a substantial economic burden to the Australian economy of approximately $1.7 billion annually1,2. 

Rural Australian populations experience a higher skin cancer burden when compared to their metropolitan counterparts3,4. While lifetime risk of diagnosis of melanoma skin cancer and NMSC is increasing, the mortality for both types of skin cancer remains low5,6. Rural populations have a higher melanoma mortality rate when compared to metropolitan areas7. Those living in the state of Victoria and outside major cities are 44% more likely to be diagnosed with melanoma, with the highest likelihood of diagnosis in the South West Victoria region8. Given NMSCs are not reportable conditions, it is difficult to ascertain whether the same trends exist. These differences in incidence and mortality have been attributed to a combination of an ageing rural population, the increased occupational risk from UV exposure (such as for farmers in rural regions), and inequities in service availability between metropolitan and rural areas7.

Australian GPs manage over half of Australia’s skin cancer cases, constituting approximately 3% of all GP patient presentations9,10. Patients experiencing socioeconomic disadvantage, and rural Australians, are more likely to have their skin cancers diagnosed and managed in primary care, reflecting the financial and geographical accessibility of GPs10. As of the 2021/2022 medical workforce analysis, there were 39 259 GPs nationally, of whom 9629 practised in Victoria and 416 were practising in rural locations11. GPs are responsible for investigating, diagnosing and managing the array of skin presentations in rural areas as approximately 92% of specialised dermatologists are based in metropolitan centres12. While skin cancer detection is included in the Royal Australian College of General Practitioners’ training curriculum, there is a paucity of formalised training, with clinicians relying on external courses or on-the-job training5,13. As a result, considerable variations have been identified in GP confidence in diagnosis and management of skin cancers, largely due to the requirements of GPs in rural settings to be multi-skilled, variable opportunities to participate in specialised training and those with a particular interest incorporating skin cancer as a speciality in their practice5. GPs able to accurately detect skin cancer early minimised both the morbidity and mortality burden, with delays in diagnosis of stage I melanoma increasing the mortality risk by 5%14-16.

Existing literature has covered the epidemiology of skin cancer in rural populations across various states, yet there is limited research specifically focused on Victoria17. This clinical review addresses this gap by investigating the detection of melanoma skin cancer and NMSC in a rural general practice in the South West region of Victoria. The clinic location is categorised as a medium rural town by the Modified Monash Model (MM 4), but also serves a broader agricultural area of small rural towns (MM 5), serving a population of about 16 50018.

Methods

This clinical review was a retrospective data audit of patient files for two different time periods: 14 October 2019 to 5 November 2020 and 2 February 2021 to 20 February 2022. Due to the impact of the COVID-19 pandemic, the time periods were unable to be exactly 1 year apart. A retrospective study design provides an efficient process in data analysis and is a practical methodology in terms of managing datasets19.

Participants and data collection

A file review was completed in the clinic’s electronic medical records (ZedMed) of all Medicare item numbers billed for skin cancer and presumed skin cancer excisions (items 31356 to 31376) for all doctors for the periods of 14 October 2019 to 5 November 2020 and  1 February 2021 to 17 February 2022. Clinical information was cross-checked with hard-copy treatment room records.

Data collection focused on complete excisions of skin cancers only, not on any lesions that were treated non-surgically after a diagnostic biopsy. Neither punch nor shave biopsies were included in the dataset, to streamline data collection.

Lesions that were re-excised where surgical margins were inadequate were only counted as a single procedure. Multiple excisions from different anatomical locations from the same patient were counted as separate procedures.

Statistical analysis

Data were reported as mean, range and standard deviation (SD) where appropriate. All p-values less than 0.05 were considered statistically significant. Statistical analysis was conducted using STATA v17 (StataCorp; https://www.stata.com) (Tables 1–3).

Number needed to treat (NNT) is a measurement of the impact of medicine or medical intervention by estimating the number of patients that need to be treated in order to have an effect on one person, and it is a common metric for evaluating skin cancer detection13.

When applied to skin cancer detection in this retrospective analysis, NNT is a ratio calculated to determine the total number of patients that need to be treated, to prevent one incidence of skin cancer, calculated individually for each cancer, thus representing the ratio of benign skin lesions excised for every confirmed malignancy13,20. It was calculated by dividing the total number of lesions excised by the number of malignant lesions excised and rounded to the nearest whole number.

table image

In the setting of this retrospective research, the number needed to treat (NNT) is a concept to provide a measurement of diagnostic accuracy in melanoma detection, where the ratio reflects the number of benign pigmented lesions removed for each melanoma13. It is suggested that the lowest NNT results are associated with dermatologists, followed by GP skin cancer specialists20. A lower NNT has been linked with improved patient care by aiding in earlier detection and reducing unnecessary biopsies13,20.

Diagnostic accuracy was calculated to assess how experience affects the pre-procedural diagnostic ability of each clinician. In this context it is a more specific measure than NNT as it calculates if a clinician’s exact pre-procedural diagnosis was in keeping with the histology report. Where NNT is a more general measure, diagnostic accuracy provides context on how experience and diagnostic skills are linked.

A diagnosis was found to be correct if the preoperative notes suggested a lesion was a basal cell carcinoma (BCC) and the histology confirmed a BCC. If the pre-procedural diagnosis was a squamous cell carcinoma (SCC) and the lesion was histologically a BCC or a melanoma, this was still graded as inaccurate.

table image

A companion article explores administered anaesthetic (volume/dose), complications (dehiscence/infection), patient and clinician demographics over the same time periods21.

Ethics approval

Ethics approval was granted by Deakin University Human Research Ethics Committee (DUHREC) (approval number 2022-177).

Results

Across the study periods, a total of 789 lesions were excised from 575 patients, of which 449 (56.9%) lesions were histologically confirmed to be malignant (Table 1). Patient ages ranged between 17 and 99 years, with mean ages for men and women of 68.3 and 65.5 years, respectively. In male patients 62.2% of lesions excised were histologically confirmed to be malignant, while in females the proportion of malignant lesions was much lower, at 49.7%. There was a corresponding statistically significant difference in malignancy rates between genders (p≤0.001).

Preoperatively, 681 lesions were suspected to be malignant. Table 2 compares the preoperative clinical diagnosis with the histological diagnosis. The preoperative diagnostic category ‘aesthetic’ refers to lesions the clinician believed to be benign but the patient wanted removed for cosmetic purposes. Overall, GPs were mostly correct in identifying malignancies, especially for NMSCs, whereas melanomas were more difficult to correctly identify. Regarding NMSCs that were correctly identified, BCCs were diagnosed 63.8% of the time and SCCs 59.1%. Melanomas were only identified correctly 15.6% of the time; however, considering the difficulty in diagnosis, this is expected19,22.

There were similar numbers of excisions across the head and neck, trunk and limbs (Fig1). NMSCs were more commonly removed from sun-exposed areas of the body such as the head and neck, and limbs. There were differences between the locations of SCCs and BCCs. BCCs had a greater occurrence on the head and neck, while SCCs were more common on the limbs. In contrast, melanoma was predominantly found on the trunk. 

A total of 15 GPs removed lesions, with experience ranging from registrar level to specialist GP skin practitioners. Table 3 presents the number of removals and diagnostic accuracy by years of experience in general practice. Using the aforementioned NNT calculation approach, the NNTs for melanoma and NMSC were 5.4 and 1.4, respectively.

Table 1: Skin cancer type by patient gendertable image

Table 2: Histological skin lesion diagnosis compared with preoperative diagnostic category in a rural clinic in South West Victoria, Australia, 14 October 2019 – 5 November 2020 and 1 February 2021 – 17 February 2022table image

Table 3: GP diagnostic accuracy compared to years of general practice experience in a rural clinic in South West Victoria, Australia, 14 October 2019 – 5 November 2020 and 1 February 2021 – 17 February 2022table image

table image Figure 1: Location and histology of excised lesions.

Discussion

This study examined the NNT and incidence of skin cancer in a rural general practice in South West Victoria. The location is in an MM 4 location that also services a wider agricultural geographic area of MM 5 due to the scarcity of primary healthcare services in the area.

Epidemiology

A total of 789 lesions were removed from 575 patients across two distinct time periods. The data were collected as part of a broader investigation into skin cancer excisions.

A total of 56.9% of excisions were histologically confirmed to be malignant. The anatomical distribution of skin malignancies aligned with trends reported in existing research2,23,24.

Males were significantly more likely to be diagnosed with skin cancer. Notably, there was an over-representation of males diagnosed with melanoma compared to the statewide average25. This difference occurred despite the practice catchment exhibiting a gender ratio comparable to the statewide figure26. While comparative data for NMSC are unavailable due to it not being a reportable condition, it is known rural males are significantly more likely to be diagnosed with cancer than metropolitan males27.

The higher rates of skin cancer among rural males may be attributed to the occupational profile of the rural workforce, with a higher percentage of male farmers and outdoor workers7. Additionally, rural males are more likely to recognise personal skin cancer risk factors, self-examine their skin and seek skin checks than their metropolitan counterparts20,28,29.

Melanoma and non-melanoma skin cancer

This study determined the NNT for melanoma is 5, a significantly lower figure than for other research findings13,29,30. Australian literature, focusing on skin cancer detection in primary care, estimates the NNT range for melanoma to be 9.4–4013,28,29, while an international meta-analysis estimated the NNT for melanoma was 20,22,2320. The broad range in melanoma NNT across the literature reflects the diversity within the GP workforce. GPs with a special interest in skin cancer are often those working in areas with a higher prevalence of skin cancer, achieving a lower NNT13,20,28. The prevalence of skin cancer in regional Australia is another factor contributing to improved NNT due to increased caseloads and exposure frequency13,30-33.

As expected, the NNT for NMSC was lower than for melanoma. This is due to the challenge in distinguishing subtle skin changes associated with melanoma. Furthermore, melanomas are less common and, due to their high mortality risk, clinicians often adopt a more conservative approach19,33. The calculated NNT for NMSC was 1, which aligned with other Australian studies, with an NNT range for NMSC of 1.5–1.729,34.

While there is no ideal NNT, a lower value is often preferred as it generally reflects a higher diagnostic accuracy, fewer unnecessary excisions and a reduction in associated morbidity and economic burden29,30. However, a low NNT may signify too narrow an excision criterion being used, resulting in under-excision of lesions30.

The low NNT for both melanoma and NMSC in this study may be attributable to the increased experience of rural GPs, due to the locality and specialist maldistribution of the Australian workforce. National data reports the number of GPs per 1000 people is highest among MM 4 locations, at 1.3 per 1000, but this decreases to 0.8 per 1000 in MM 5 locations35. Clinics such as the one in this research are within an MM 4 region. MM 4 areas often have a larger ratio of catchment area to population and consequently have more scope and responsibility than their metropolitan counterparts9,12.

There are significantly fewer non-GP specialists in MM 4 and MM 5 locations, at 0.4–0.1 per 1000, 4.5 times lower than in MM 3 locations35. While these statistics are nationwide and do not account for the heterogeneity within rural Australia, they do provide insight into the increased and broad experience rural GPs develop compared to their urban counterparts.

GP diagnostic accuracy

This study used diagnostic accuracy to evaluate its relationship with GP experience. Diagnostic accuracy, rather than NNT, was used as it allowed comparison between pre-procedural and histological diagnosis, providing a more specific reflection of diagnostic skill.

Our results indicate a positive association between increasing GP experience and diagnostic accuracy, and this result aligns with previous research13,20. GPs with more than 20 years of experience demonstrated the highest diagnostic accuracy for melanoma skin cancer and NMSC, at 17% and 68%, respectively. Interestingly, GPs with 6–19 years of experience exhibited a lower diagnostic accuracy for melanoma compared to their less-experienced counterparts. In contrast, those with 0–5 years of experience showed an interest in skin cancer management but lacked the general practice medicine expertise of more senior colleagues. In existing literature, there is substantial variability in the reported diagnostic accuracy for GPs13,20,32. Determining the true diagnostic skill within the workforce is difficult due to the broad range of clinician interest, training, clinical exposure and patient demographic characteristics.

GPs with 6–19 years of experience conducted the fewest procedures within this study. This is attributed to their clinical area of interest, and their demographic characteristics. While it is known that having a special interest in skin cancer increases a GP’s diagnostic accuracy, the impact of clinical interest on the availability of timely skin cancer care is not well documented36,37. This highlights a potential area of further research as there are increasing numbers of skin cancer presentations, often outweighing practitioner availability, especially in rural settings where health service capacity is stretched38-40.

Limitations

Several limitations within this study have been identified. It is unclear whether these results are transferrable to other rural settings in Australia, as there is considerable variation in healthcare availability, climate and demographics across the country, particularly in rural MM 4 and MM 5 settings. Moreover, this study was a subset of a larger intervention study that spanned two discrete time periods. While the intervention was not relevant to the data used, it is not known whether it resulted in a subconscious change in behaviour in GPs. As the larger study did not include shave or punch biopsies or delineate between in-situ and invasive lesions, these data were not available. Due to the retrospective nature of this research, some data may have been incomplete and absent due to inconsistent documentation available. Also, this study design did not account for patients who may have been referred to local surgeons or out-of-town dermatology services, which may potentially impact the estimates of NNT and diagnostic accuracy.

Conclusion

This study examined the demographic characteristics of rural skin cancer patients and the skin cancer diagnostic skills of GPs in South West Victoria. To our knowledge there is little existing research on this region of Australia specific to this topic. Results revealed males were significantly more likely to be diagnosed with skin cancer. This may be attributed to the occupational profile of the rural community and health-seeking behaviour of rural males. This study also found a lower NNT for melanoma and NMSC compared to existing Australian research, likely reflecting the increased pressure on rural GPs to diagnose skin cancer. Moreover, the diagnostic accuracy was demonstrated to increase with clinician experience and for clinicians with a special interest in skin cancer. However, there is limited large-scale research available for comparison. Given the vital role of GPs in skin cancer management, the diagnostic accuracy of Australian GPs should be further investigated.

references:

1 Melanoma Institute Australia. Melanoma Facts. Available: web link (Accessed 20 February 2023).
2 Staples MP, Elwood M, Burton RC, Williams JL, Marks R, Giles GG. Non-melanoma skin cancer in Australia: the 2002 national survey and trends since 1985. Medical Journal of Australia 2006; 184(1): 6-10. DOI link, PMid:16398622
3 Australian Institute of Health and Welfare. Rural, regional and remote health: indicators of health status and determinants of health: Summary. 2008. Available: web link (Accessed 25 December 2023).
4 Adelson P, Sharplin GR, Roder DM, Eckert M. Keratinocyte cancers in South Australia: incidence, geographical variability and service trends. Australian and New Zealand Journal of Public Health 2018; 42(4): 329-333. DOI link, PMid:29972285
5 Smith AL, Watts CG, Robinson S, Schmid H, Chang CH, Thompson JF, et al. GPs' involvement in diagnosing, treating, and referring patients with suspected or confirmed primary cutaneous melanoma: a qualitative study. BJGP Open 2020; 4(2): bjgpopen20X101028. DOI link, PMid:32295791
6 Australian Institute of Health and Welfare. Skin cancer in Australia: Summary. 2016. Available: web link (Accessed 25 December 2023).
7 Coory MD, Ho T, Jordan SJ. Australia is continuing to make progress against cancer, but the regional and remote disadvantage remains. Medical Journal of Australia 2013; 199(9): 605-608. DOI link, PMid:24182226
8 Cancer Council Victoria. Making cancer care equitable for all Victorians. [Victorian Cancer Registry]. 2023. Available: web link (Accessed 25 December 2023).
9 Whiting G, Stocks N, Morgan S, Tapley A, Henderson K, Holliday EG, et al. General practice registrars' use of dermoscopy: Prevalence, associations and influence on diagnosis and confidence. Australian Journal for General Practitioners 2019; 48(8): 547-553. DOI link, PMid:31370131
10 Reyes-Marcelino G, McLoughlin K, Harrison C, Watts CG, Kang YJ, Aranda S, et al. Skin cancer-related conditions managed in general practice in Australia, 2000-2016: a nationally representative, cross-sectional survey. BMJ Open 2023; 13(5): e067744. DOI link, PMid:37142316
11 Australian Government Department of Health and Aged Care. General practice workforce providing primary care services in Australia. Available: web link (Accessed 24 December 2023).
12 Adelson P, Eckert M. Skin cancer in regional, rural and remote Australia; opportunities for service improvement through technological advances and interdisciplinary care. Australian Journal of Advanced Nursing 2020; 37(2). DOI link
13 Rosendahl C, Williams G, Eley D, Wilson T, Canning G, Keir J, et al. The impact of subspecialization and dermatoscopy use on accuracy of melanoma diagnosis among primary care doctors in Australia. Journal of the American Academy of Dermatology 2012; 67(5): 846-852. DOI link, PMid:22325462
14 Doran CM, Ling R, Byrnes J, Crane M, Searles A, Perez D, et al. Estimating the economic costs of skin cancer in New South Wales, Australia. BMC Public Health 2015; 15(1): 952. DOI link, PMid:26400024
15 Higashi MK, Veenstra DL, Langley PC. Health economic evaluation of non-melanoma skin cancer and actinic keratosis. Pharmacoeconomics 2004; 22(2): 83-94. DOI link, PMid:14731050
16 Guy GP, Ekwueme DU. Years of potential life lost and indirect costs of melanoma and non-melanoma skin cancer: a systematic review of the literature. Pharmacoeconomics 2011; 29(10): 863-874. DOI link, PMid:21846158
17 Richard MA, Grob JJ, Avril MF, Delaunay M, Gouvernet J, Wolkenstein P, et al. Delays in diagnosis and melanoma prognosis (II): the role of doctors. International Journal of Cancer 2000; 89(3): 280-285. DOI link, PMid:10861505
18 Australian Government Department of Health and Aged Care. Health workforce locator. 2019. Available: web link (Accessed 1 December 2024).
19 Argenziano G, Soyer HP. Dermoscopy of pigmented skin lesions – a valuable tool for early diagnosis of melanoma. Lancet Oncology 2001; 2(7): 443-449. DOI link, PMid:11905739
20 Petty AJ, Ackerson B, Garza R, Peterson M, Liu B, Green C, et al. Meta-analysis of number needed to treat for diagnosis of melanoma by clinical setting. Journal of the American Academy of Dermatology 2020; 82(5): 1158-1165. DOI link, PMid:31931085
21 Eaton J, Feeney J, Dopheide T, Beattie J, Jaipurwala R, Fuller L, et al. Not just tachycardia: A pilot study examining wound-healing complications associated with the dose and volume of lignocaine in skin cancer excisions. Australian Journal of General Practice 2024; 53(8): 558-562. DOI link, PMid:39099120
22 Rosendahl C, Tschandl P, Cameron A, Kittler H. Diagnostic accuracy of dermatoscopy for melanocytic and nonmelanocytic pigmented lesions. Journal of the American Academy of Dermatology 2011; 64(6): 1068-1073. DOI link, PMid:21440329
23 Youl PH, Janda M, Aitken JF, Del Mar CB, Whiteman DC, Baade PD. Body-site distribution of skin cancer, pre-malignant and common benign pigmented lesions excised in general practice. British Journal of Dermatology 2011; 165(1): 35-43. DOI link, PMid:21443534
24 Buettner PG, Raasch BA. Incidence rates of skin cancer in Townsville, Australia. International Journal of Cancer 1998; 78(5): 587-593. DOI link
25 Arroyo GP, Lofters A, Clarkson E. Pharmacological management of common soft tissue lesions of the oral cavity. Oral and Maxillofacial Surgery Clinics of North America 2022; 34(1): 99-114. DOI link, PMid:34728147
26 Victorian Government Department of Health. Melanoma. Available: web link (Accessed 25 December 2023).
27 Carli P, de Giorgi V, Chiarugi A, Nardini P, Weinstock MA, Crocetti E, et al. Addition of dermoscopy to conventional naked-eye examination in melanoma screening: a randomized study. Journal of the American Academy of Dermatology 2004; 50(5): 683-689. DOI link, PMid:15097950
28 Rolfe HM. Accuracy in skin cancer diagnosis: a retrospective study of an Australian public hospital dermatology department. Australasian Journal of Dermatology 2012; 53(2): 112-117. DOI link, PMid:22571558
29 Glenister K, Bougoulias M, Zgibor J, Bourke L, Simmons D. Self-reported skin cancer-related behaviours in rural Victoria: results from repeat cross-sectional studies in 2001-2003 and 2016-2018. Australian and New Zealand Journal of Public Health 2022; 46(3): 382-386. DOI link, PMid:35238449
30 Goodwin BC, Rowe AK, Crawford-Williams F, Baade P, Chambers SK, Ralph N, et al. Geographical disparities in screening and cancer-related health behaviour. International Journal of Environmental Research and Public Health 2020; 17(4): 1246. DOI link, PMid:32075173
31 Hansen C, Wilkinson D, Hansen M, Argenziano G. How good are skin cancer clinics at melanoma detection? Number needed to treat variability across a national clinic group in Australia. Journal of the American Academy of Dermatology 2009; 61(4): 599-604. DOI link, PMid:19664848
32 Baade PD, Youl PH, Janda M, Whiteman DC, Del Mar CB, Aitken JF. Factors associated with the number of lesions excised for each skin cancer: a study of primary care physicians in Queensland, Australia. Archives of Dermatology 2008; 144(11): 1468-1476. DOI link, PMid:19015421
33 English DR, Del Mar C, Burton RC. Factors influencing the number needed to excise: excision rates of pigmented lesions by general practitioners. Medical Journal of Australia 2004; 180(1): 16-19. DOI link, PMid:14709122
34 Nelson KC, Swetter SM, Saboda K, Chen SC, Curiel-Lewandrowski C. Evaluation of the number-needed-to-biopsy metric for the diagnosis of cutaneous melanoma: a systematic review and meta-analysis. JAMA Dermatology 2019; 155(10): 1167-1174. DOI link, PMid:31290958
35 Youl PH, Baade PD, Janda M, Del Mar CB, Whiteman DC, Aitken JF. Diagnosing skin cancer in primary care: how do mainstream general practitioners compare with primary care skin cancer clinic doctors? Medical Journal of Australia 2007; 187(4): 215-220. DOI link, PMid:17708723
36 Moffatt CRM, Green AC, Whiteman DC. Diagnostic accuracy in skin cancer clinics: the Australian experience. International Journal of Dermatology 2006; 45(6): 656-660. DOI link, PMid:16796621
37 FitzGerald KL, Buttner PG, Donovan SA. Nonpigmented skin lesions – how many are nonmelanoma skin cancer? Australian Family Physician 2006; 35(7): 555-557.
38 Australian Government Department of Health and Aged Care. Review of the DPA Classification System. 2022. Available: web link (Accessed 25 December 2023).
39 Tran H, Chen K, Lim AC, Jabbour J, Shumack S. Assessing diagnostic skill in dermatology: a comparison between general practitioners and dermatologists. Australasian Journal of Dermatology 2005; 46(4): 230-234. DOI link, PMid:16197420
40 National Rural Health Alliance. Skin cancer in Australia: awareness, early diagnosis and management – House of Representatives Standing Committee on Health. 2014. Available: web link (Accessed 23 December 2023).

You might also be interested in:

2015 - Regional universities and rural clinical schools contribute to rural medical workforce, a cohort study of 2002-2013 graduates

2014 - Healthcare use and prescription of opioids in rural residents with pain

2009 - Survey of a videoconference community of professional development for rural and urban nurses