Page 2 of 17 JDDG manuscript proof How to run a an effective and efficient dermato- oncology unit.
Short title: How to run a dermato-oncology unit
Simone (S) van der Geer*, Hajo (H.A) Reijers**, Gertruud (G.A.M) Krekels***
For Peer Review
Department of Dermatology, Rotterdam, the Netherlands.
** Eindhoven University of Technology, School of Industrial Engineering, Eindhoven,
*** Catharina Hospital Eindhoven, Department of Dermatology, Eindhoven, the
JDDG manuscript proof JDDG manuscript proof Page 3 of 17
The worldwide incidence of skin cancer (especially non-melanoma skin cancer) has
risen dramatically over the last decades. Skin cancer, including pre-malignancy is
becoming a chronic disease. Adjustments in skin cancer health care need to be
made. A disease management system for skin cancer is mandatory in order to avoid
waiting lists and insure adequate treatment quality with ever growing numbers of
patients requiring (surgical) treatment. At the Catharina Hospital Eindhoven
For Peer Review
being made on several levels of the dermato-oncology unit in
collaboration with Eindhoven University of Technology. The model combines
technological improvements, with training of health care workers, training General
Practioners and prevention of skin cancer. In this article we will discuss our ideas and
clinical experiences on managing a dermato-oncology unit.
JDDG manuscript proof Page 4 of 17 JDDG manuscript proof For Peer Review JDDG manuscript proof JDDG manuscript proof Page 5 of 17
The worldwide incidence of skin cancer (especially non-melanoma skin cancer) has
risen dramatically over the last decades.[1,2]
Estimates show that one in five persons will be diagnosed with skin cancer in their
life time.[1] This is probably an underestimate because adequate registration of these
For Peer Review
acking in many countries.[2] Traditionally, the incidence is highest in
the elderly (> 65 years), 438 per 100,000 person-years.[3] There is a world-wide rise
in skin cancer incidence of at least 5% annually.[3] This increase will continue for at
least two decades, and is caused by a growing aging population as well as an
increase of UV exposure (solar and artificial).[3]
A second patient group consists of organ transplant patients who develop multiple
lesions. Although rates differ across various countries, the number of patients
receiving organ transplants is increasing. In the Netherlands 1,100 persons had
organ transplants in 2007, which is an increase of 28% compared to 2006.[4] Since
the improvement of graft survival has resulted in increased survival for transplant
patients, the number of survivors has increased accordingly. However, this
phenomenon is paired with a longer duration of immune suppressive medication
resulting in more skin malignancies.[5,6] Nearly 50% of all renal transplant patients
develop skin cancers within 20 years after transplantation.[6]
The younger adult population (15-34 years) is a third large patient group. In this
group, it is predicted that skin cancer incidence will double from 322 incident cases in
With a population that is aging and a skin cancer incidence that is on the rise in the
younger population, a growing amount of patients will be confronted with multiple
new tumours for the rest of their lives. In addition, many of these patients have skin
JDDG manuscript proof Page 6 of 17 JDDG manuscript proof
pre-malignancies as well.[7,8,9,10] Skin cancer and pre-malignancy is becoming a
chronic disease with a disease burden comparable to other chronic diseases.
The increased prevalence has resulted in many dermatologists needing to allocate
more of their time to these problems. An evaluation of the diagnosis-treatment codes
of a large outpatient dermatology clinic at the Catharina-Hospital Eindhoven in the
Netherlands shows that over 50% of dermatologists’ time is spent on skin cancer and
For Peer Review
n lesions. This is only the tip of the iceberg. If no changes are
planned for the health care system, this will result in dermatologists’ work being
limited to skin malignancies and pre-malignancies, resulting in less attention paid to
other dermatology patients. Consequently, adjustments in skin cancer health care
need to be made. A disease management system for skin cancer is mandatory in
order to avoid waiting lists and ensure adequate treatment quality with ever growing
numbers of patients requiring (surgical) treatment.
In the literature, few articles are available about the management of a dermatology
practice. The latest articles date back to 2000, discussing general adjustments for
dermatology clinics to achieve the best possible business outcome.[11,12,13] No
literature at all is available about running a dermato-oncology unit, i.e. how to deal
with an increasing amount of skin cancer patients while maintaining quality of care.
Few articles describe specialty clinics for the dermatologic care of solid-organ
transplant patients.[14,15] They emphasize the importance of an organized and
firmly established clinic model to allow proactive and ongoing care for these patients.
Close communication with the team of transplant physicians, education of other
health care providers, an effective scheduling mechanism and patient education are
all described as key points to provide the best care.
JDDG manuscript proof JDDG manuscript proof Page 7 of 17
At the Catharina Hospital Eindhoven, adjustments are being made on several levels
of the dermato-oncology unit. In this so called “disease management system for skin
cancer”, we are working closely together with the Eindhoven University of
Technology. In the past 5 years it has shown to be possible to accommodate an
increase of 20% in skin cancer patients at the Catharina Hospital. Workflow
technology will help in further reorganizing this dermato-oncology unit so that it will
be capable of facilitating an annual increase of at least 5% skin cancer patients. We
For Peer Review
eas and clinical experiences with respect to developing the disease
First of all, prevention is one of the most important strategies to influence the rapidly
increasing incidence of skin cancer. Prevention campaigns should increase attention
to young children and their parents, with a focus on UV protection throughout life.
Prevention however, will not influence the rising skin cancer incidence and
prevalence on a short term basis. As a result -- unfortunately -- it is not an important
subject for health care insurances. The sense of urgency among dermatologists that
skin cancer is becoming an expensive disease (in the U.S skin cancer has taken the
fifth position with respect to cancer costs) [16], has not resulted in providing financial
stimulus for prevention campaigns by governments nor insurance companies.
Primary prevention and secondary prevention should go hand in hand and
dermatologists should play an important role in educating patients and future patients
in how to reduce the risk of chronic skin malignancy.
JDDG manuscript proof Page 8 of 17 JDDG manuscript proof
General practioners (GP) should be trained to recognize skin malignancies and
diagnose them at an early stage. This will lead to smaller skin malignancies, which
are less difficult and less expensive to treat than large malignancies.[17] We are
preparing a large scale training programme for general practioners to recognize and
treat actinic keratosis (AK). In an unpublished survey among GP’s, it was stated that
they have difficulties in recognizing AK and find it important to be trained and
For Peer Review
gnizing and treating AK. Many patients with chronic skin
(pre)malignancy could be followed by the GP and/or a nurse practioner who is
stationed at the GPs office once a week. It will be sufficient to see these patients in
the dermato-oncology clinic only if the GP is in doubt about the diagnosis, if a
squamous cell carcinoma is suspected (and early excision is required) or if there are
severe adverse events occurring during treatment. Teledermatology could help to
improve efficiency of patient referrals and patient care.[18,19]
GP’s should also be involved in prevention campaigns and in the after-care of treated
patients (for instance, remove stitches and inform patients of complete or incomplete
tumour-removal). A continuous medical education programme for GP’s (e-learning
and training), will reduce unnecessary or late referrals.
In the Catharina Hospital, we started in 2004 with a training programme for dermato-
oncology nurses. This resulted in special trained dermato-oncology nurses, nurse
practioners and physician assistants. Depending on their educational background
and clinical experience they perform multiple tasks to relieve the workload for the
dermatologists at our dermato-oncology unit.
Biopsies and small standard excisions, including the closure of small defects , are
performed by these employees with supervision of a dermatologist. They also
perform photodynamic therapy and cryotherapy, give local anesthesia, remove
JDDG manuscript proof JDDG manuscript proof Page 9 of 17
stitches, and give information on (primary and secondary) prevention and treatments.
They inform the patient about the diagnosis, treatment and follow-up. Workflow
management helps to reduce the number of hospital visits and dermato-oncology
nurses are available to give adjuvant information (mostly by email) in case the
patients has a question. A dermatologist is available in the background if needed.
Nurse care management interventions have been shown to improve medical,
psychosocial and lifestyle outcomes in patients with chronic diseases such as
For Peer Review
or et al show that nurse care managers, working closely with the
patients’ GP and using evidence based algorithms, can improve medical outcomes,
without increasing physician visits.[20] A review of a nurse-led care in dermatology
concludes that nurses are managing and treating a number of dermatological
conditions, primarily using treatment protocols. Patients report various benefits such
as faster access to treatment, reduction in referral to the general practitioner or
dermatologist and an increase in knowledge of their condition.[21]
To improve work efficiency, quality of care and patient satisfaction, a modern
information technology system is needed. Together with Eindhoven University of
Technology, we are shaping an information technology system that in the first place
will allow to consult, manipulate and retrieve patient-related data. Furthermore, the
system shall be pro-active and allow diagnostic and treatment advice for clinically
Over the past years, insights have been gained on how such clinical decision support
could be effectively integrated into the care process.[22] The system will also be
developed such that communication amongst the health care teams is facilitated, for
instance, assisting nurses in ascertaining which actions need to be executed or have
already been completed for patients.[23] The potential of this technology has not
JDDG manuscript proof Page 10 of 17 JDDG manuscript proof
been fully exploited in the healthcare domain in general, and certainly not for skin
For instance, by using a workflow system at our dermato-oncology unit, it was
possible to increase the number of photodynamic treatments performed by a
dermato-oncology nurse from 7 to 10 per day. Workflow technology will also be
beneficial to further streamline the allocation of work, to monitor work in progress,
and analyze effectiveness of treatment patterns for patient subgroups.
For Peer Review
ent resulting from the application of IT is the use of email-contact for
patients with their dermato-oncology nurse. This reduces the number of telephone-
calls (which are more time-consuming then emails) and improves the patient-
Instant diagnosis by histopathology should be available to diminish the number of
hospital visits and telephone calls. In the Catharina Hospital we are using fresh
frozen sections on biopsies on clinically well defined BCC, immediately at the first
visit in the hospital. The fresh frozen sections are examined by one of the Mohs
surgeons as well as a pathologist to confirm the diagnosis. Patients will be informed
about the diagnosis the same day. If planned properly, an excision could take place
as follow-up immediately by a physician assistant. In other cases, Mohs Micrographic
surgery or PDT can be performed immediately after and follow-up appointments can
By this so-called “One-stop-shop diagnosis and treatment”, less appointments are
needed (reducing the burden on the healthcare system,) and on the other hand it will
improve quality of medical care (especially for most elderly patients and their
relatives less hospital visits are extremely welcome).
JDDG manuscript proof JDDG manuscript proof Page 11 of 17
For pigmented lesions and squamous cell carcinoma, direct excision is possible on a
Various treatment modalities are available for dermato-oncology patients.
Dermatologists need to use all these modalities in an efficient way. Treatments can
easily be combined.[25,26,27,28,29] Periods that patients are in the hospital need to
For Peer Review
ntly as possible. While patients are waiting in between Mohs
micrographic surgery (MMS) rounds for their aggressive BCC in the face, we perform
For patients with very extensive skin malignancies, like patients with the Nevoid
Basal Cell Carcinoma Syndrome, we perform megasessions under general
anesthesia. In these treatment sessions, we treat multiple lesions with various
techniques (MMS, surgical excision, PDT).[30,31]
In addition, several treatments exist that can be used by the patient at home. This will
of course diminish the workload at the outpatient clinic. Patients are able to contact a
nurse practioner or special trained nurse if they have questions about the treatment,
Finally, treatment options need to be based on optimal treatment results.
Unfortunately, for surgical treatments randomized controlled trials on margins,
histopathological examination, etc. are limited. Recently, 5-years results on MMS
have become available and these indicate less recurrences after MMS for recurrent
facial BCC.[32] In the past, MMS was considered to be time-consuming, and this
was a reason not to perform MMS. By incorporating a histopathology lab into the
dermatology clinic, it is possible to increase efficiency for MMS. In the Catharina
Hospital we perform 6 MMS procedures combined with multiple excisions (for
pigmented lesions, Squamous cell carcinoma), PDT and One-stop-shop for BCC .
JDDG manuscript proof Page 12 of 17 JDDG manuscript proof
Skin cancer, including pre-malignancy, is becoming a chronic disease. The
enormous increase in skin cancer will force dermatologists to make adjustments in
how they run their unit. The disease management system that is set up at the
Catharina Hospital Eindhoven is one of the ways to provide an answer to the ever
increasing number of patients that need to be treated for skin cancer, but an effective
one at that. The system, which is still expanded and developed, combines
For Peer Review
rovements (for instance workflow technology to maximize the
number of MMS or PDT treatments) with training of health care workers (nurses,
nurse practioners, Physician Assistants, GP’s, etc). Additionally, there is a focus on
early recognition of lesions by patients and GP’s, as well as on prevention of skin
Finally, the use of One-stop-shop (by the use of frozen sections, already available for
MMS) can furthermore increase efficiency. We hope that our ideas and experiences
can serve as an inspiration for setting up other dermatolo-oncology units.
Key words: dermato-oncology, skin cancer, management
JDDG manuscript proof JDDG manuscript proof Page 13 of 17 References
1. Rigel DS, Friedman RJ, Kopf AW. Lifetime risk for development of skin
cancer in the U.S. population: Current estimate is now 1 in 5. J Am Acad
2. Vries de E, Rhee van der H, Coebergh JWW. Trends, oorzaken, aanpak en
gevolgen van de huidkankerepidemie in Nederland en Europa. Ned Tijdschr
For Peer Review
, Poll-Franse van de LV, Louwman WJ, Gruijl de FR, Coebergh
JWW. Predictions of skin cancer incidence in the Netherlands up to 2015. Br
4. Dutch transplant society (Nederlandse transplantatie stichting).
http://www.transplantatiestichting.nl/files/misc/persbericht_nts_2008.pdf.
5. Moloney FJ, Comber H, O’Lorcain P, O’Kelly P, Conlon PJ, Murphy GM. A
population-based study of skin cancer incidence and prevalence in renal
transplant recipients. Br J Dermatol 2006; 154: 498-504.
6. Carroll RP, Ramsay HM, Fryer AA, Path FMRC, Hawley CM, Nicol DL,
Harden PNl. Incidence and prediction of nonmelanoma skin cancer post-renal
transplantation: a prospective study in Queensland, Australia. Am J Kidney
7. Marcil I, Stern RS. Risk of developing a subsequent nonmelanoma skin
cancer in patients with a history of nonmelanoma skin cancer. Arch Dermatol
8. Collins GL, Nickoonahand N, Morgan MB. Changing demographics and
pathology of nonmelanoma skin cancer in the last 30 years. Semin Cutan
JDDG manuscript proof Page 14 of 17 JDDG manuscript proof
9. Karagas MR, Greenberg ER, Spencer SK, Stukel TA, Mott LA. Increase in
incidence rates of basal cell and squamous cell skin cancer in New
Hampshire, USA. Int J Cancer 1999; 81: 555-559.
10. Ramchandran S, Fryer AA, Smith A, Lear J, Bowers B, Jones PW, Strange
RC. Cutaneous basal cell carcinomas. Distinct host factors are associated
with the development of tumors on the trunk and on the head an neck.
For Peer Review
DL. Dermatology practice management assures practice
development and efficiency. Sem Cutan Med Surg 2000; 19: 170-172.
12. Baker KE. Will a physician assistant improve your dermatology practice? Sem
13. Nestor MS. Dermatology practice management enhancement: implications for
dermatology in the age of managed care. Sem Cutan Med Surg 2000; 19:
14. Christenson LJ, Geusau A, Ferrandiz C, Brown CD, Ulrich C, Stockfletch E,
Berg D, Orengo I, Shaw JC, Carucci JA, Euvrard S, Pachego T, Stasko T,
Otley CC. Specialty clinics for the dermatologic care of solid organ transplant
recipients. Dermatol Surg 2004; 30: 598-603.
15. Ismail F, Mitchell L, Casabonne D, Gulati A, Newton R, Proby CM, Harwood
CA. Specialist dermatology clinics for organ transplant recipients significantly
improve compliance with photoprotection and levels of skin cancer
awareness. Br J Dermatol 2006; 155: 916-925.
16. Housman TS, Feldman SR, Williford PM, Fleischer AB, Goldman ND,
Acostamadiedo JM, Chen GJ. Skin cancer is among the most costly of all
cancers to treat for the Medicare population. J Am Acad Dermatol 2003; 48:
JDDG manuscript proof JDDG manuscript proof Page 15 of 17
17. Smeets NW, Krekels GA, Ostertag JU, Essers BA, Dirksen CD, Nieman FH,
Neumann HA. Lancet 2004; 364(9447): 1766-72.
18. Moreno-Ramirez D, Ferrandiz L, Nieto-Garcia A, Carrasco R, Moreno-
Alvarez P, Galdeano R, Bidegain E, Rios-Martin JJ, Camacho FM. Store-and-
forward teledermatology in skin cancer triage. Arch Dermatol 2007; 143: 479-
19. May C, Giles L, Gupta G. Prospective observational comparative study
For Peer Review
the role of store and forward teledermatology triage in skin cancer.
20. Barr Taylor C, Houston Miller N, Reilly KR, Greenwald G, Cunning D, Deeter
A, Abascal L. Evaluation of a nurse-care management system to improve
outcomes in patients with complicated diabetes. Diabetes Care 2003; 26:
21. Courtenay M, Carey N. A review of the impact and effectiveness of nurse-led
care in dermatology. J Clin Nurs 2007; 16: 122-8.
22. Fieschi M, Dufour JC, Staccini P, Gouvernet J, Bouhaddou O. Medical
decision support systems: old dilemmas and new paradigms? Methods Inf
23. Maviglia SM, Zielstorff RD, Paterno M, Teich JM, Bates DW, Kuperman GJ.
Automating complex guidelines for chronic disease: lessons learned. J Am
24. Lenz R, Reichert M. IT Support for healthcare processes premises,
challenges, perspectives. Data Knowledge Engineering 2007; 61: 39-58.
25. Kuijpers DI, Smeets NW, Krekels GA, Thissen MR. Photodynamic therapy as
adjuvant treatment of extensive basal cell carcinoma treated with Mohs
micrographic surgery. Dermatol Surg 2004; 30: 794-8.
26. Thissen MR, Kuijpers DI, Krekels GA. Local immune modulator (imiquimod
5% cream) as adjuvant treatment after incomplete Mohs micrographic surgery
JDDG manuscript proof Page 16 of 17 JDDG manuscript proof
for large, mixed type basal cell carcinoma: a report of 3 cases. J Drugs
27. Tsjui T, Otake N, Nishimura M. Cryosurgery and topical fluorouracil : a
treatment method for widespread basal cell epithelioma in basal cell nevus
28. Strange PR, Lang PG. Long-term management of basal cell nevus syndrome
with topical tretinoin and 5-fluorouracil. J Am Acad Dermatol 1992; 27: 842-
For Peer Review
29. Krunic AL, Viehman GE, Madani S, Clark RE. Microscopically controlled
surgical excision combined with ultrapulse CO2 vaporization in the
management of a patient with the nevoid basal cell carcinoma syndrome. J
30. Geer van der S, Ostertag JU, Krekels GAM. Treatment of basal cell
carcinomas in patients with nevoid basal cell carcinoma syndrome. J Eur
31. Geer van der S, Krekels GAM, Verhaegh ME. Treatment of the Nevoid Basal
Cell Carcinoma Syndrome patient in a megasession. A case series. Dermatol
32. Mosterd K, Krekels GA, Nieman FH, Ostertag JU, Essers BA, Dirksen CD,
Steijlen PM, Vermeulen A, Neumann HAM, Kelleners-Smeets NWJ. Surgical
excision versus Mohs micrographic surgery for primary and recurrent basal
cell carcinoma of the face; a prospective randomised controlled trial with 5-
years’ follow-up. Lancet Oncol 2008 Dec; 9(12): 1149-56. Epub 2008 Nov 17.
JDDG manuscript proof
Hydration and nutrition The BCUHB website has links to the documents and policies described in this leaflet. The effects of dementia on food and fluid intake and hence nutritional status can be considerable. Ongoing nutritional screening and regular monitoring are important. Refer to the Guidance on the use of the Do Not Attempt BCUHB Adult Nutritional Support Policy for guidance on
a quick guide to symptoms , treatment and prevention Healthy Respect @ Lothian NHS Board NHS Lothian, Deaconess House, 148 Pleasance Edinburgh EH8 9RS Tel 0131 536 9454 Email [email protected] www.healthy-respect.com C aught Chlamydia? You have been diagnosed with an infection called Chlamydia. At your appointment today you willhave been given a lot of