1. THE 7TH SYMPTOM
LYMPHEDEMA IN ADVANCED CANCER
Madeleine Fiddes
Rural CNS and Lymphedema Therapist
Hospice Waikato
Hospice NZ Palliative Conference
29-31st October 2014
2. Overview
• Definition of lymphedema
• Types of lymphedema
• Stages of lymphedema
• Lymphedema and Palliative Care
• Treatment options
• Collaboratively in the community
• Case Studies
• Conclusion
3. Lymphatic system
Lymphatic system is part of circulatory system. Network
of vessels and nodes throughout the body transporting
lymph fluid from tissues back to bloodstream.
Functions: Assist immune system
Remove waste products (ALA, 2014)
4.
5. Lymphedema
“Lymphedema is a progressive chronic condition. It leads
to excessive accumulation of protein rich lymph fluid in
the tissues as a result of lymphatic failure due to either
congenital abnormality or damage to the lymphatic
system.” (British Lymphology Society, 2010)
7. Primary Lymphedema
Mechanical insufficiency due to unknown cause
Congenital defect of lymphatic system
• Milroy’s disease
• Lymphedema Praecox – up to age 35 (at puberty)
• Lymphedema Tardis –
after age 35 (milder condition)
10. Lymphedema and Palliative Care
“Lymphedema is known to affect the physical,
psychological and social well-being of the patient”
(Tobin et al, 1995).
“Lymphedema in palliative care is associated with
worsening levels of function and dependence as
well as feelings of hopelessness, disgust and
social isolation” (Hewitt et al, 2010).
11. Oedema
• Oedema:
• Excess low-viscosity, protein-poor interstitial fluid
that exceeds lymphatic capacity to reabsorb
• Lymphedema:
• Excess protein-rich interstitial fluid within skin and
sub-cutaneous tissue resulting from lymphatic
dysfunction
12. Differential diagnosis:
Oedema/lymphedema - Advanced Cancer
• Obstruction - DVT, compression by tumour
• Hypoalbuminemia
• Renal/hepatic failure
• Cardiac failure
• Dependant limb, immobility, neurological deficit
• Effects of drugs or cytotoxic chemotherapy
• Infection – e.g. Cellulitis
• Malignant involvement or infiltration of lymphatic
structures – e.g. SVCO
(Towers et al. 2010)
13. Principles of Palliative management
• Reverse the reversible
• Patient’s priorities and goals
• Benefit versus burden
• Patient general condition and prognosis
• Psychosocial issues
Vaugn Keeley ALA conference, 2014
Explanation - Compassion - Education
14. Key concepts:
Palliative Care and Lymphedema
• Uniqueness of each patient
• Interdisciplinary (team) work
• Communication
• Ingenuity and creativity
• Good control of pain and other symptoms
• Maintenance of independence
• Fears and expectations
• Self-care (Towers et al 2010)
15. We need to continually ask: Is the
primary goal life prolongation or is it
comfort and quality of life?
17. Key components of care
• Skin care
• Remedial exercise
• Lymphatic drainage therapy
• Compression – bandaging/garments
• Kinesio® Taping
“The Power of Touch”
18. Differences Standard and Palliative CDT
Standard CDT
• Goal – reduce swelling,
transition to garment, life-long
maintenance
• Four elements CDT
• Two distinct phases in
treatment
• Definitive contra-indicators to
treatment
Palliative CDT
• Goal – comfort, support, relief
of symptoms, maintain
function
• CDT elements modified or
omitted
• Less distinction between
phases
• Contra-indicators relative
(Towers et al, 2010)
19. Standard and Palliative Bandaging
Standard
• Full standard pressure
• Multi-layer bandaging
• 24-hour bandaging during
the intense phase
• Foam padding used
• Transition to compression
garments
Palliative
• Reduced pressure
• Fewer layers required
• Intensive treatment for
lymphorrhea require
frequent re-application
• Bandaging lower leg/s
• Soft padding better
tolerated
• May transition to lighter
compression garment
• (Towers et al, 2010)
20. Management of LE in the community
Green (2010); Warilow& Jones (2012); Morgan P (n.d.)
• Patient
• GP
• Lymphedema Therapist
• Community Nurse
• Interdisciplinary approach
21. Developing: Integrated LE patient pathway
• Referral process
• Central point of entry
• Multidisciplinary focus
• Development of study days
“It is important that practitioners use standard
assessment tools and documentation (Hopkins, 2010).
29. “Mary”
• 53 yr. old woman
• Stage 4 Leiomyosarcoma – uterus
• Hysterectomy, Bilateral Oophorectomy
• Pleomorphic Sarcoma R arm and extensive bony
metastasis
30.
31. Conclusion
“Although lymphedema can be challenging to
manage in palliative populations, it is possible to
modify existing modalities to effectively reduce
oedema and improve quality of living”
(Hewit et el, 2010)
32. 2015 National Hui
NZ Lymphedema Therapists
Date: 16 – 17th May 10 - 5pm
Venue: Hamilton Airport Hotel
201, Airport Road, RD2, Hamilton
34. Useful web-sites
• Lymphoedema Support Network www.lymphoedema.org
• Australia Lymphology Association
• International Lymphoedema Framework www.lympho.org
• Lymphoedema DermNet NZ
• National Lymphoedema Network
• Lymph notes www.lymphnotes.com
• British Lymphology Society www.thebls.com
• Lymphoedema Support Network www.lymphoedema.org/lsn
• LymphCare
35. References
• Towers, A. et al. (2010). Care of palliative patients with
cancer related lymphedema. J. of Lymphoedema. 5(1).
• Morgan. P. Health Professionals ideal roles in
lymphoedema management. BJ of Community Nursing.
• Green, T. (2010). Key-worker clinics: the maintenance
phase of LE therapy. Chronic Oedema, October.
• Hopkins, A. 2010). Mapping an integrated LE patient
pathway. 5(2).
36. References
• Todd, M. (2009). Understanding lymphoedema in advanced
disease in palliative setting. IJPN. 15(10).
• Hewitt, B., et el. (2010). Lymphoedema in Palliative Care.
Cancer Forum, 34(2).
• Cooper, G. (2012). Lymphoedema treatment in palliative care:
a case study. British Journal of Nursing. 21(15).
• Board, J., & Anderson, J. (2013). Treatment of lymphorrhea.
British Journal of Healthcare Assistants. 7(1).
• Todd, M (2010). Managing lymphoedema in palliative care
patients. BJN. 18(8).
• Linnitt, N. (2005). Lymphoedema: recognition, assessment and
management. Woundcare. March.
• Fenton, S. (2001). The power of touch in last week of life. IJPN.
17(2)
37.
38. My Role
• Rural CNS
• Lymphedema Therapist –
Casey-Smith Method
• Registered ALA - member
Hinweis der Redaktion
Lymph system is a network of vessels that form a semi-circle.
Starts in tissue bed with lymphatics
Fluid moves one way, starting from the interstitial tissue.
Valves ensure the fluid moves one way only.
No pump. Muscle movement acts as a pump.
Lymph Fluid
Lymph fluid carries - large proteins, dead cells, bacteria, cancer cells
Originates as blood plasma.
Most of the plasma / fluid returns back into the blood circulation via the small veins.
A small percentage returns to blood circulation via the lymph circulation.
National Breast and Ovarian Ca Centre
Estimated 20% of breast, genituiry, Gynea or Melanoma
Vulval 36-47%, Breast 20%, Cervical 24%, Melanoma 9 -29%, following SNB 4 -8 %
Primary
Primary lymphedema result from -
Hypoplasia – small and ineffective vessels
Hyperplasia – tangle of vessels
Aplasia – absence of lymph vessels
Milroy's disease - characterized by lymphedema, commonly in the legs, caused by congenital abnormalities in the lymphatic system. Disruption of the normal drainage of lymph leads to fluid accumulation and hypertrophy of soft tissues.
Filariasis –
Most common cause secondary LE – caused by a parasitic worm roundworm/larvae migrate to the lymphatics.
These filarial worms are spread by a mosquito vector.
Wuscheria bancrofti carry out their life cycle in two hosts. Human beings serve as the definitive host and mosquitoes as their intermediate hosts. The adult parasites reside in the lymphatics of the human host.
According to WHO 2000 – 120milj – 45 milj is severely disfigured
Eradication
The WHO is coordinating an effort to eradicate filarisis. The mainstay of this programme is the mass use of antifilarial drugs on a regular basis for at least five years
In April 2011, Sri Lanka was certified by the WHO as having eradicated this disease.
Phases – Acute, Latent and chronic
As lymphoedema develops, the protein rich fluid is gradually replaced by fibro-sclerotic tissue.
This will result in ‘non-pitting’ or ‘woody’-feel to the limb
Stage 0 (sub-clinical phase)
No measurable evidence of swelling
Heaviness/pain/pins and needles
Stage 1
Some swelling evident
‘Pits’ on pressure
Subsides with elevation
Stage 2
Limb elevation no longer reduce swelling
Fibrosis – pitting less evident
Poor skin condition
Stage 3
Pitting is absent
Fibrotic changes
Holistic approach is very important
Managing lymphedema in PC is an important part of holistic care
Palliative patients can benefit from LE Management
Reduced function, immobility
Pain reduction – heaviness of limb, lymphorrhea
Infection minimisation – recurrent infections
Skin protection
Psychological support – fear and anxiety
Explanation – Compassion - Education
DVT’s are common in the hyper-co-arguable state that exist with mets cancer – the advent of low molecular heparin has simplified anti-coagulation. However use of compression and exercise remains controversial
Cardiac Failure – drugs – calcium antagonists, alpha-blockers, anti-hypertensive drugs
Hypoalbuminemia – anorexia, cachexia, ascitis – repeated drainage
Drugs – NSIADS (non steriodal inflammatory), hormonal therapies, pregabalin, bisposphonates especially Zometa,
Reversible – anaemia, ascitis and superior vena cave obstruction
Understand and respect uniqueness of patient
Inclusion of family in providing lymphedema care
Involvement of community in providing resources/care
Interdisciplinary (team) work
Attention to detail – what is important to the patient?
Good communication – patient, family and other providers
Ingenuity/creativity in dealing with therapeutic problems
Good symptom control of pain and other symptoms
Maintenance if independence and function
Focus of meaning of symptoms - fears/expectations
Attention to therapist own emotions with limited prognosis
The burden of the treatment must not exceed the benefit to the patient. (Honnor, 2008)
Patient – enable to take responsibility of his/her own care and management of LE
Provide education programmes of information
Availability of written, verbal and other information e.g. videos
Develop plans of care in partnership with patient and carers
Encourage and enable patients to use information technologies to learn more
GP role – Early diagnosis of LE
Differential diagnosis e.g. HF and DVT
Diagnostic investigations
Awareness and early referral to LE services
LE specialist – management and supervision of LE services.
Management of community based clinics
LE assessments, MLD
Assist and teach SLD
Develop a central referral system.
Auditing
Education
Key-worker – qualified health professional
Nurses identified for LE clinics had skills in leg ulcer management and tissue viability – current skills and capacity could be used to support patients within this settings.
Facilitate and develop LE support groups
Clear pathway for management of LE
Roles and skills of CNS and key worker clearly defined
Treatment carried out by staff member with appropriate training
Cost effective service
Patient discharged from community clinics within agreed protocols
Education program covered from anatomy/physiology – assessment – four key components
Patient Summary:
· 07/02/12: Clear cell carcinoma of the urethra, T4 (vagina, bladder neck) N2 (3/9) Mx (? clitoral), Stage IV.
· 19/04/12: Radical cystourethrectomy, hysterectomy, bilateral oophorectomy, vaginectomy, vulvectomy, pelvic lymph node dissection and formation of ileal conduit (anterior exenteration).
· 10/04/13: Restaging subcutaneous metastases, small volume pelvic disease.
· 18/04/13: Lymphoedema of the left leg managed conservatively. Repeat palliative radiation to bony lesion in the left pubis. Stage IV disease (symphysis pubis involvement).
· 1/9/2013: Skin lesion mons pubis slight fungation, manage conservatively
21/01/2008, wide local excision left breast plus modified B-reconstruction and axillary sentinel lymph node; pT1a(2.5mm) pNo cMx, Grade 2, invasive ductal carcinoma. No LVSI. ER 3+ 80%, PR 3+ 60 – 70% and HER2 2+, FISH not amplified. Adjuvant radiotherapy to the left breast, 50gy in 25 fractions. Tamoxifen discussed but not advised/started due to low risk.
· October 2013, presented with extensive skin and breast changes in both breasts.
· 24/10/2013, punch biopsy right breast, Grade 2/3 carcinoma, with ulceration and infiltration of the dermis. No Paget’s disease. ER 1+ (15%), PR negative, HER2 negative, cN3 cM1(skin), Stage IV disease.
· 08/11/2013, commenced on AC chemotherapy. Due to toxicities, this was stopped January 2014.
· March 2014, disease progression chest wall, extensive skin involvement from flank to flank. Further chemotherapy recommended but declined.
· 22/07/2014, re-referred with progressive disease with fungation right breast as well as increasing right arm lymphoedema with evidence of progressive lymphadenopathy, lower cervical/supraclavicular/axillary regions with brachial plexus involvement.
Treatment
Skin care, MLD – husband – gave them some time to be intimate