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Lymphatic Research and Biology logoLink to Lymphatic Research and Biology
. 2019 Apr 17;17(2):202–210. doi: 10.1089/lrb.2019.0015

LIMPRINT Study: The Turkish Experience

Pinar Borman 1,,2,, Christine Moffatt 3, Susie Murray 4, Aysegul Yaman 1, Merve Denizli 1, Meltem Dalyan 5, Sibel Unsal-Delialioğlu 5, Sibel Eyigör 6, Figen Ayhan 5, Burcu Duyur Çakıt 5, Secil Vural 5, Oya Özdemir 1,,2, Eda Kurt 7, Evrim Coşkun Çelik 8, Lale Cerrahoğlu 9, Müge Kepekçi 10, Fusun Terzioğlu 11, Ayşe Arikan Donmez 2,,12
PMCID: PMC6639105  PMID: 30995192

Abstract

Background: Lymphedema and chronic edema is a major health care problem in both developed and nondeveloped countries The Lymphoedema Impact and Prevelance - International (LIMPRINT) study is an international health service-based study to determine the prevalence and functional impact in adult populations of member countries of the International Lymphoedema Framework (ILF).

Methods and Results: A total of 1051 patients from eight centers in Turkey were recruited using the LIMPRINT study protocol. Data were collected using the core and module tools that assess the demographic and clinical properties as well as disability and quality of life (QoL). Most of the Turkish patients were recruited from specialist lymphedema services and were found to be women, housewives, and having secondary lymphedema because of cancer treatment. The duration of lymphedema was commonly <5 years and most of them had International Society of Lymphology (ISL) grade 2 lymphedema. Cellulitis, infection, and wounds were uncommon. The majority of patients did not get any treatment or advice before. Most of the patients had impaired QoL and decreased functionality, but psychological support was neglected. Although most had social health security access to lymphedema centers, nevertheless access seemed difficult because of distance and cost.

Conclusion: The study has shown the current status and characteristics of lymphedema patients, treatment conditions, the unmet need for the diagnosis and treatment, as well as burden of the disease in both patients and families in Turkey. National health policies are needed for the prevention, diagnosis, and treatment in Turkey that utilize this informative data.

Keywords: lymphedema, lymphoedema, chronic edema, LIMPRINT, quality of life, impact

Introduction

Lymphedema is an incurable, debilitating, and progressive condition, characterized by persistent swelling of one or more parts of the body, because of the impairments in lymph transport. This chronic and progressive disease can occur at any time after cancer surgeries, can arise from congenital malformation of the lymphatic system, or because by damage to lymphatic vessels.1,2 It is a major health care problem in both developed and nondeveloped countries. It is serious because of its long-term physical and psychosocial consequences for the patients, if left untreated. When lymphedema is not diagnosed and treated in the earlier stages, the prognosis for these patients is worse and treatments are more costly. Lymphedema frequently leads to physical, emotional, and psychological challenges and impairs the quality of life (QoL) if it is underrecognized and undertreated.3,4 Treatment cost of lymphedema has also been identified as a barrier. The support and funding of medical conditions and complex care needs will ease the stress and treatment burden associated with lymphedema.5 There are also challenges of managing complex lymphedema patients with obesity, and those associated with chronic medical conditions and wounds.6 Therefore the awareness of this chronic condition by both health professionals and patients—knowledge comprising the characteristics of lymphedema patients, difficulties finding appropriate treatments or funding for care, and the impact of disease on functional, psychosocial status, and QoL are of great importance, especially in developing countries.

Lymphedema has been a rising condition in Turkey over the past 10–12 years. Awareness about lymphedema was low and the treatment methods were unknown and certified lymphedema specialists were lacking until recent years.7 There are no data about the incidence of lymphedema in Turkey. Patient characteristics or experiences of some patients are reported in some small studies.7–9

The LIMPRINT© study is an international multisite health service-based study to determine the prevalence and functional impact of lymphedema/chronic edema in the adult population of member countries of the International Lymphoedema Framework (ILF). It aims to estimate the proportion of patients with chronic edema and those with a concurrent wound.

Turkey has been a member of the ILF since 2017 under the auspices of the Anatolian/Turkish Lymphedema Association (ALA), but the LIMPRINT study was first noticed by Dr. Borman, Chair of the ALA at the ILF Meeting in Glasgow, 2014 (www.ilfconference.org). She was influenced by the presentations from other countries and was interested to find out how a study of Turkish lymphedema patients could be made and compare it with different countries. The participation in LIMPRINT study would be valuable and provide important information about the demographic, social, and QoL characteristics of Turkish patients. The study results would show the current status and characteristics of lymphedema patients, treatment conditions, the unmet need for diagnosis and treatment of those suffering with the condition, and burden of the disease in both patients and families in Turkey. The LIMPRINT study would also allow the comparison with different populations from different countries. In addition the data would be informative for developing national health polices and reimbursement procedures in diagnosis and treatment of lymphedema in Turkey.

Materials and Methods

Considering all these points, an interest in being part of LIMPRINT was shared with the executive members of ALA, and after unanimous approval, a request for Turkey to be involved was officially made in 2014 and accepted by the ILF.

Two main institutions are related to lymphedema in Turkey: Anatolian Lymphedema Association and Hacettepe University Lymphedema Practice and Research Center. Therefore the participation in this international multicenter study proposal was sent to the health professional delegates of the ALA from different parts of Turkey working in centers who are managing patients with lymphedema. In addition, Hacettepe University Lymphedema Practice and Research Center actively engaged and recruited a great number of patients in collaboration with the Department of Physical Medicine and Rehabilitation. Vascular surgeons and nurses were also informed. Most of the surgeons were not interested in joining the study. After this initial information the proposal was sent to 10 centers with 8 accepting to be part of the study.

The local steering groups were Anatolian (Turkish) Lymphedema Association and Hacettepe University Lymphedema Practice and Research Center. The stakeholders were as follows, from five different areas of the country:

  • (1)

    University of Hacettepe Faculty of Medicine Department of Physical Medicine and Rehabilitation (PMR) and Hacettepe University Lymphedema Research and Practice Center (Dr. Pınar Borman, Dr. Merve Denizli, Dr. Ayşegül Yaman, Dr. Oya Özdemir, Dr. Fusun Terzioğlu, and Ayşe Arikan Dönmez).

  • (2)

    Ankara Rehabilitation Training and Research Hospital (Dr. Meltem Vural, Dr. Sibel Ünsal Delialioğlu).

  • (3)

    Ankara Training and Research Hospital Clinic of PMR (Dr. Figen Ayhan, Dr. Burcu Duyur Çakıt, Dr. Seçil Vural).

  • (4)

    Kirsehir Ahi Evran University Department of PMR (Dr. Eda Kurt).

  • (5)

    Ege University Medical Faculty Department of PMR, İzmir (Dr. Sibel Eyigör).

  • (6)

    Istanbul Rehabilitation Training and Research Hospital Clinic of PMR (Dr. Evrim Coşkun Çelik).

  • (7)

    Istanbul Kanuni Sultan Süleyman Education and Research Hospital (Dr. Muge Kepekçi).

  • (8)

    Manisa Celal Bayar University Medical Faculty Department of PMR (Lale Cerrahoğlu).

All centers gained approval from their local ethical committees. The coordinator of the Turkish study was the chair of ALA and director of the HU Lymphedema Practice and Research Center—P.B. All the LIMPRINT questionnaires were translated to Turkish and back translated to ensure accuracy of language. The QoL questionnaires lymphedema quality of life (LYMQOL)-arm and LYMQOL-leg10 did not have Turkish validation. The cross-cultural Turkish validation studies of the LYMQOL-arm and LYMQOL-leg questionnaires were performed before this study began adding further validity to the methods.11,12 Then the Turkish data collection forms were sent to the included centers. All the centers filled the questionnaires and sent them by ordinary mail to the coordinator and they were then returned when completed in batches of 30. Data entry was undertaken from one center (Hacettepe University) with each center given an individual code.

The patients were recruited to the study according to the inclusion and exclusion criteria of the LIMPRINT study protocol. Data were collected using a Core Tool to determine the prevalence of chronic edema and a set of five Module Tools to assess the impact of chronic edema on the lives of sufferers. Data were entered into a secure central on-line database. The core tools included questions about type of facility in which data are collected, demographics, level of obesity, mobility, relevant comorbidities, classification and history of lymphedema, cellulitis history, categories of treatment, site of swelling, wound area, access to treatment, and subjective control of swelling. The module tools comprised demographics and disability, QoL, details of swelling, wounds, and cancer. The Turkish version of World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0) was used to assess disability,13,14 and LYMQOL10–12 and European Quality of Life Five Dimensional Questionnaire (EQ-5D)15,16 tools were used to assess QoL.

WHODAS 2.0 is a validated 12-item disability assessment schedule. It includes questions exploring the patient's personal circumstances for example, housing, employment, and education.14,15

LYMQOL is a validated condition-specific QoL assessment instrument (it is not validated for patients with lymphatic filariasis) that assesses the impact of lymphedema on the patient's everyday living and health-related QoL. There is a tool for patients with lymphedema of the upper limb and one for the lower limb.11–13

EQ-5D is a generic QoL instrument applicable to a wide range of health conditions and provides a simple descriptive profile and single index value for health status.15 EQ-5D is primarily intended for self-completion and is simple and quick to complete. Turkish validation has previously been made and used in this study.16

Results

A total of 1051 patients from eight centers of five different geographical areas took part in the study. Most of the patients were recruited from specialist lymphedema services. The majority of patients were women, housewives, nonobese, had full range of movement, and walked independently. The most common comorbidity was diabetes followed by hypertension. Half the patients stated that their edema was not under control. The core demographic properties of the patients are given in Table 1.

Table 1.

The Core Data of Turkish Patients Comprising the Demographic and Disease-Related Variables (N = 051)

  n (%)
Type of facility
 Acute inpatient 53 (5.04)
 Acute outpatient 426 (40.53)
 General practitioner 1 (0.10)
 Nursing home 2 (0.19)
 Specialist Lymphoedema Centre 569 (54.14)
Gender
 Female 980 (93.24)
 Male 71 (6.76)
Age
 Mean (minimum, maximum) 53.42 (7–85)
 Median 54
Age groups, years
 5–14 5 (0.48)
 15–44 231 (21.98)
 45–64 615 (58.52)
 65–74 161 (15.32)
 75–84 38 (3.62)
 85 plus 1 (0.10)
Obesity
 Under weight 14 (1.33)
 Normal weight 630 (59.94)
 Obese 357 (33.97)
 Morbidly obese 50 (4.76)
Lower limb mobility
 Bed bound 10 (0.95)
 Chair bound 13 (1.24)
 Walks with aid 71 (6.76)
 Walks unaided 957 (91.06)
Upper limb mobility
 No function 3 (0.29)
 Limited range of movement 138 (13.13)
 Full range of movement 910 (86.58)
Comorbidity
 Diabetes mellitus 210 (19.98)
 Heart failure/ischemic heart disease 84 (7.99)
 Neurological disease 33 (3.14)
 Peripheral arterial disease 115 (10.94)
 None of these 711 (67.65)
Subjective control of swelling
 Yes 393 (48.70)
 No 414 (51.30)

The classification of lymphedema was mostly secondary (85%) and caused by cancer (79%) with 85% suffering from breast cancer, followed by venous insufficiency, lipedema, immobility, and obesity. The cellulitis and infection or hospitalization for cellulitis and infection were infrequent. The duration of lymphedema was <5 years in majority of the patients. The whole group disease characteristics and distribution of variables according to gender are given in Table 2.

Table 2.

The Turkish Edema Characteristics in the Core Tool (N = 051)

  Total (N = 1051) Female (n = 980) Male (n = 71) χ2 (df) or p-value
Classification
 Primary 152 (14.48) 129 (13.18) 23 (32.39) 19.75 (1)
 Secondary 898 (85.52) 850 (86.82) 48 (67.61) <0.001
Secondary swelling
 Cancer 717 (79.58) 698 (81.92) 19 (38.78) 53.09 (1)
 Noncancer 184 (20.42) 154 (18.08) 30 (61.22) <0.001
Cancer-related secondary LE
 Treatment related 715 (99.72) 696 (99.71) 19 (100.0) 0.99a
 Metastatic 8 (1.12) 7 (1.00) 1 (5.26) 0.19a
Noncancer-related secondary LE
 Venous 92 (50.0) 71 (46.10) 21 (70.00) 0.017
 Immobility 48 (26.09) 36 (23.38) 12 (40.00) 0.058
 Obesity 84 (45.65) 74 (48.05) 10 (33.33) 0.14
 Lymphatic filariasis 5 (2.72) 4 (2.6) 1 (33.3) 0.99a
 Noncancer other 57 (30.98) 51 (33.12) 6 (20.00) 0.16
Duration
 <6 Months 273 (26.00) 260 (26.56) 13 (18.31)  
 6 Months to 1 year 128 (12.19) 122 (12.46) 6 (8.45)  
 1–2 Years 142 (13.52) 133 (13.59) 9 (12.68) 6.64 (5)
 2–5 Years 219 (20.86) 201 (20.53) 18 (25.35) 0.25
 5–10 Years 146 (13.90) 136 (13.89) 10 (14.08)  
 10+ Years 142 (13.52) 127 (12.97) 15 (21.13)  
History of cellulitis
 Yes 232 (22.07) 206 (21.02) 26 (36.62) 9.37 (1)
 No 819 (77.93) 774 (78.98) 45 (63.38) 0.002
Infection in last year
 Yes 171 (73.71) 149 (72.33) 22 (84.62) 1.80 (1)
 No 61 (26.29) 57 (27.67) 4 (15.38) 0.18
Lower limb swelling
 Yes 426 (40.57) 367 (37.49) 59 (83.10) 57.12 (1)
 No 624 (59.43) 612 (62.51) 12 (16.90) <0.001
Upper limb swelling
 Yes 628 (59.81) 615 (62.82) 13 (18.31) 54.56 (1)
 No 422 (40.19) 364 (37.18) 58 (81.69) <0.001
a

Fisher's exact test.

LE, lymphedema.

The treatment categories of the patients are given in Table 3. The majority of patients did not get any treatment or advice before (66.4%). The most common treatment was exercise (50%), skin care advice (47%), massage (43%), and compression garment (40%). Psychological support was neglected in 91% of patients. A great number of patients expressed that their swelling was not under control. In Turkey the complex decongestive therapy is free in government hospitals for patients with obligative health insurance. Therefore the majority of the attendants replied to this question that treatment was free. But the cost of bandages for multilayer short stretch bandaging are not reimbursed and the amount of compression garments are only partially reimbursed in Turkey. Nearly 40% of the patients stated that if the treatment was not free, they could not cover the expenses for the treatment. Most of the patients suggested that lymphedema treatment was available for free within a reasonable travelling distance, as they are living in big cities or metropoles, but more than one third of them declared that the distance would prevent patients from accessing specialized centers. As the majority of patients did not have wounds or complicated lymphedema, they were not related to discharge from hospital or long stays in care centers (Table 4).

Table 3.

The Treatment Categories (N = 051)

  All patient (N = 1051), n (%) Female (n = 980), n (%) Male (n = 71), n (%) χ2 (df) or p-value
No treatment offered
 No 698 (66.41) 652 (66.53) 46 (64.79) 0.09 (1)
 Yes 353 (33.59) 328 (33.47) 12 (35.21) 0.76
Skin care advice
 No 552 (52.52) 516 52.65) 36 (50.70) 0.10 (1)
 Yes 499 (47.48) 464 (47.35) 35 (49.30) 0.75
Wound dressing
 No 1020 (97.05) 957 (97.65) 63 (88.73) 18.40 (1)
 Yes 31 (2.95) 23 (2.35) 8 (11.27) <0.001
Antibiotic
 No 934 (88.87) 880 (89.80) 54 (76.06) 12.63 (1)
 Yes 117 (11.13) 100 (10.20) 17 (23.94) <0.001
Massage
 No 594 (56.52) 553 (56.43) 41 (57.57) 0.04 (1)
 Yes 457 (43.48) 427 (43.57) 30 (42.25) 0.83
Physiotherapy
 No 963 (91.63) 902 (92.04) 61 (85.92) 3.24 (1)
 Yes 88 (8.37) 78 (7.96) 10 (14.08) 0.07
Compression garment
 No 638 (60.70) 599 (61.12) 39 (54.93) 1.06 (1)
 Yes 413 (39.30) 381 (38.88) 32 (45.07) 0.30
Multilayer bandage
 No 716 (68.13) 669 (68.27) 47 (66.20) 0.13 (1)
 Yes 335 (31.87) 311 (31.73) 24 (33.80) 0.72
Pneumatic compression pumps
 No 903 (85.92) 846 (86.33) 57 (80.28) 2.00 (1)
 Yes 148 (14.08) 134 (13.67) 14 (19.72) 0.16
Debulking—lipedema—lymphatic surgery
 No 1042 (99.14) 971 (99.08) 71 (100.00)  
 Yes 9 (0.86) 9 (0.92) 0 (0) 0.99a
Exercise advice
 No 517 (49.19) 479 (48.88) 38 (53.52) 0.57 (1)
 Yes 534 (50.81) 501 (51.12) 33 (46.48) 0.45
Cellulitis advice
 No 811 (77.16) 761 (77.65) 50 (70.42) 1.96 (1)
 Yes 240 (22.84) 219 (22.35) 21 (29.58) 0.16
Psychological support
 No 963 (91.63) 900 (91.84) 63 (88.73) 0.83 (1)
 Yes 88 (8.37) 80 (8.16) 8 (11.27) 0.36
Complex decongestive therapy
 No 1035 (98.48) 965 (98.47) 70 (98.59) 0.99a
 Yes 16 (1.52) 15 (1.53) 1 (1.41)  
Control of swelling
 No 414 (51.30) 372 (49.80) 42 (70.00) 9.07 (1)
 Yes 393 (48.70) 375 (50.20) 18 (30.00) 0.003
a

Fisher's exact test.

Table 4.

The Questions Related to Access, Distance, and Patient Costs of Treatment (n = 009)

  Total (%) Female (%) Male (%) χ2 (df) or p-value
(1) Are patients' entire treatment complex decongestive therapy free?
 Yes 779 (77.21) 730 (77.49) 49 (73.13) 0.68 (1)
 No 230 (22.79) 212 (22.51) 18 (26.87) 0.41
(2) If it is not free, could the patient cover the treatment expenses?
 Yes 538 (61.14) 504 (61.61) 34 (54.84) 1.11 (1)
 No 342 (38.86) 314 (38.39) 28 (45.16) 0.29
(3) Is lymphedema treatment available in a reasonable distance?
 Yes 785 (77.95) 753 (80.02) 32 (48.48) 35.69 (1)
 No 222 (22.05) 188 (19.98) 34 (51.52) <0.001
(4) Does the distance prevent the patient from accessing a specialist center?
 Yes 302 (36.39) 276 (35.84) 26 (43.33) 1.35 (1)
 No 528 (63.61) 494 (64.16) 34 (56.67) 0.25
(5) Do patients' lymphedema/wounds prevent discharge from hospital?
 Yes 47 (10.26) 35 (8.47) 12 (26.67) 14.58 (1)
 No 411 (89.74) 378 (91.53) 33 (73.33) <0.001
(6) Is the patient's lymphedema/wound the main reason for remaining in long-term care?
 Yes 79 (17.59) 63 (15.40) 16 (40.00) 15.20 (1)
 No 370 (82.41) 346 (84.60) 24 (60.00) <0.001
(7) Is the patient's lymphedema/wound the main reason for remaining in long-term home care?
 Yes 50 (11.47) 40 (10.05) 10 (26.32) 9.04 (1)
 No 386 (88.53) 358 (89.95) 28 (73.68) 0.003

According to the demographics in the module data, most patients were in the age range of 45–64 years and were living with their partners or relatives. Eighty percent of the patients were owner occupiers and 55% had their own vehicle. As most of the patients were housewives, they were not the main provider for their family. Fifty-two percent of the attendants had primary school education with only 20% having a university diploma. As most patients were housewives (55%), they (92%) did not have to change or stop their job/work that would affect their family income (Table 5).

Table 5.

Demographic Characteristics (n = 048)

  n (%)
Living with
 No one/live alone 109 (10.4)
 Partner/spouse 724 (69.1)
 Other relative 212 (20.2)
 Friend 2 (0.2)
 Other 1 (0.1)
Living accommodation
 Owner occupier 838 (80)
 Public rented 11 (1.1)
 Privately rented 189 (18)
 Nursing home 5 (0.5)
 Hospital 1 (0.1)
 Supported living accommodation 4 (0.4)
Patients who had a car or other vehicle
 Yes 582 (55.5)
 No 466 (44.5)
Working/job
 Employed full time 148 (14.1)
 Employed part time 25 (2.4)
 Retired 208 (19.8)
 Unemployed looking for work 20 (1.9)
 Not working because of illness 68 (6.5)
 Looking after the house (housewives) 581 (55.4)
 Full or part-time education or training 15 (1.4)
 Other 3 (0.3)
Patients were the main provider
 Yes 202 (19.3)
 No 846 (80.7)
Age of graduation, mean ± SD, median (minimum to maximum) 16.3 ± 4.9, 17 (8–45)
Degree of graduation
 None (elementary school) 549 (52.4)
 School certificate/diploma 265 (25.3)
 University diploma/degree 215 (20.5)
 Master's degree 9 (0.9)
 Doctorate 10 (1)
Patients who had to change their job or education/training
 Yes 52 (5)
 No 996 (95)
Patients who had to stop work or education/training
 Yes 82 (7.8)
 No 966 (92.2)
Patients who had been affected/reduced their family income because of the swelling
 Yes 99 (9.5)
 No 949 (90.6)

SD, standard deviation.

The details of swelling in the module data are given in Table 6. The site of swelling was the upper extremity (arms) in 59% followed by legs (39.8%), Overall 55% did not have pitting edema. Tissues in the swollen area were mostly soft with 41% having a significant shape distortion. Thirty-six percent of the patients had not been told the reason for the swelling. Stemmer sign was positive in 75% of patients with lower extremity and 49% of patients in upper extremity swelling. The majority had ISL grade 2 swelling (61.7%) and 27.5% had ISL grade 1 lymphedema. The disability and QoL scores are given in Table 7. Most of the patients had impaired QoL and decreased functionality. These were prominent especially in lower limb chronic edema patients.

Table 6.

Details of Swelling (n = 050)

  n (%)
Pitting  
 Yes 475 (45.2)
 No 575 (54.8)
Tissue in swollen area  
 Soft 715 (68.1)
 Hard 335 (31.9)
Shape distortion in the affected limb  
 Yes 436 (41.5)
 No 614 (58.5)
Patients who had been told the reason for the swelling  
 Yes 671 (63.9)
 No 379 (36.1)
The site of swelling  
 Arm 617 (59.0)
 Leg 416 (39.8)
 Both 12 (1.2)
Stemmers sign  
 Hand—positive 313 (49.3)
 Foot—positive 329 (75.8)
Severity of the swelling  
 ISL stage I 289 (27.5)
 ISL stage II 648 (61.7)
 ISL stage III 113 (10.8)

ISL, International Society of Lymphology.

Table 7.

The Disability and Quality-Of-Life Scores (n = 050)

  Mean ± SD Median Minimum to maximum
WHODAS overall scores N = 1050 31.7 ± 21.8 27.1 0–100
EQ-5D scores (n = 1050) 0.56 ± 0.32 0.62 0.59–1
Overall health scores (n = 1050) 61.2 ± 20.5 60 0–100
LYMQOL—upper extremity (n = 630)      
 Function 17.5 ± 6.1 16 10–40
 Appearance 9.4 ± 3.6 9 5–20
 Symptoms 12.3 ± 4 12 6–24
 Emotion 11.3 ± 4.2 11 6–24
 Overall 6.6 ± 1.8 7 0–10
LYMQOL—lower extremity (n = 429)      
 Function 19.1 ± 6.4 19 8–32
 Appearance 17.5 ± 5.9 17 7–28
 Symptoms 11.8 ± 3.9 11 5–20
 Emotion 12.9 ± 4.5 12 6–24
 Overall 5.1 ± 2.1 5 0–10

EQ-5D, European Quality of Life Five Dimensional Questionnaire; LYMQOL, lymphedema quality of life; WHODAS, World Health Organization Disability Assessment Schedule.

The cancer data showed the majority (84%) had breast cancer followed by endometrium (8%), cervix (2.8%), and ovarian (2.4%) cancers. All but five of them had received treatment for cancer, with 53% having local cancer and 32% being in remission. The most common type of cancer treatment was surgery followed by chemotherapy and radiation therapy. The duration of lymphedema was <5 years in the majority of the patients (88.8%). Twenty-one percent of patients developed swelling within 3 months, 32% in 3–11 months, and 34% developed in 1–5 years after cancer treatment. The summary of cancer data is given in Table 8.

Table 8.

Details of Cancer (n = 15)

  N (%)
Patients who had treatment for cancer  
 Yes 710
 No 5
Duration between swelling and cancer treatment (How long after the cancer treatment did you develop swelling in the affected area?)  
 <3 Months 152 (21.3)
 3–11 Months 234 (32.7)
 1–5 Years 249 (34.8)
 6–9 Years 40 (5.6)
 10+ Years 32 (4.5)
 Unknown 5 (0.7)
 Not applicable 3 (0.4)
Current cancer status  
 Cured/remission 229 (32.0)
 Local cancer 383 (53.6)
 Distant metastases 56 (7.8)
 Do not know 47 (6.6)
Type of cancer  
 Bladder cancer 2 (0.3)
 Breast cancer 603 (84.3)
 Cervical cancer 20 (2.8)
 Colorectal cancer 2 (0.3)
 Endometrial cancer 57 (8.0)
 Head and neck cancer 1 (0.1)
 Melanoma cancer 6 (0.8)
 Ovarian cancer 17 (2.4)
 Vulval cancer 2 (0.3)
 Other cancer 16 (2.2)
Type of cancer treatments  
 Surgery 703 (98.3)
 Radiation therapy 569 (79.6)
 Chemotherapy 595 (83.2)
 Hormone therapy 306 (42.8)
 Molecular target therapy 16 (2.2)
 Other 1 (0.1)

The majority of patients (98%) did not have a wound. Of the patients with wounds, 55% had one to two wounds mostly grade 2 small venous ulcers with low exudate located in the legs. Most patients looked after their own wounds followed by physicians and hospital nurses. Nearly half of the wounds did not have signs of infection (47%) and had been present <6 months in the majority of the patients (70%). The wound details are given in Table 9.

Table 9.

Details of Wounds (n = 1)

  N (%)
Provider wound care  
 Physician 13 (61.9)
 Podiatrist 0
 Self-care 14 (66.7)
 Family/friend 6 (28.6)
 Hospital nurse 11 (52.4)
 Practice nurse 0
 Care home nurse 2 (9.5)
 Wound care specialist nurse 0
 Home care/community nurse 1 (4.8)
 Lymphedema specialist nurse/therapist 1 (4.8)
 Other 0
No. of wounds  
 One 7 (33.3)
 Two 9 (42.9)
 Three 2 (9.5)
 Four 1 (4.8)
 Five 1 (4.8)
 Six 1 (4.8)
 Missing 1 (4.8)
Pressure ulcer  
 None 13
 Grade 1 0
 Grade 2 5 (62.5)
 Grade 3 2 (25.0)
 Grade 4 1 (12.5)
Leg/foot ulcer cause  
 No leg/foot ulcer 6
 Venous ulcer 6 (40.0)
 Arterial ulcer 1 (6.7)
 Mixed (venous/arterial) 1 (6.7)
 Neuropathic 1 (6.7)
 Neuroischemic 0
 Other foot ulcer 2 (13.3)
 Do not know ulcer type 7 (46.7)
Acute/surgical wound  
 No acute/surgical wound 10
 Primary closure 0
 Open surgical wound 0
 Postsurgical breakdown 2 (18.2)
 Dehisced wound 5 (45.5)
 Traumatic wound 2 (18.2)
 Do not know wound type 2 (18.2)
Exudate level  
 None 9 (42.9)
 Low 7 (33.3)
 Medium 4 (19.1)
 High 1 (4.8)
Location of the wounds  
 Head or neck 21 (100)
 Arms 21 (100)
 Chest 19 (90.5)
 Abdomen 21 (100)
 Back 20 (95.2)
 Sacrum 21 (100)
 Hips 21 (100)
 Upper leg 20 (95.2)
 Groin 21 (100)
 Lower leg/ankle 9 (42.9)
 Foot 14 (66.7)
 Other 20 (95.2)
Wound area  
 Small: <10 cm2 17 (81)
 Medium: >10 and <25 cm2 4 (19.1)
 Large: >25 cm2 0
 Closed surgical wound 0
 Not applicable 0
Wound duration  
 Primary 16 (76.2)
 Recurrent 5 (23.8)
Time/duration of wounds  
 <1 Week 0
 1–2 Weeks 2 (9.5)
 2–4 Weeks 2 (9.5)
 4–6 Weeks 3 (14.3)
 6 Weeks to <3 months 4 (19.1)
 3 Months to <6 months 3 (14.3)
 6 Months to <1 year 1 (4.8)
 1 Year to <5 years 3 (14.3)
 5 Years or more 1 (4.8)
 Do not know 2 (9.5)
Wound infection  
 Yes 9 (42.9)
 No 10 (47.6)
 Unknown 2 (9.5)
Frequency of dressing change  
 Twice daily 6 (28.6)
 Daily 6 (28.6)
 Alternate days 3 (14.3)
 Two to three times per week 5 (23.8)
 Once a week 1 (4.8)
 Other 0

One of the fundamental aims of the ILF is to support countries in the development of data to establish the size of the problem of chronic edema. Such data are essential in supporting the introduction of evidence-based practice and enabling each national framework to argue for appropriate financing and reimbursement.17 According to the aims of LIMPRINT as an international epidemiological research study; the preliminary demographic results of this study provided evidence-based data for the demographic and clinical properties of Turkish lymphedema patients. The LIMPRINT study brought a great opportunity and vision to our community. The reimbursement of pressure garments was very low in grades 2 and 3 lymphedema patients in Turkey. The ALA have prepared a file for reimbursement of care about the condition and impact of lymphedema based on the results of the LIMPRINT-Turkey study. As a partner of the ILF and of the LIMPRINT study, ALA have summarized and indicated the characteristics of Turkish lymphedema patients and demonstrated their efforts for increasing the awareness and collaboration between health professionals on a national basis. The Turkish Social Security Institution has had meetings with ALA members, made rectification, and taken the decision to pay more for the reimbursement of pressure garments for lymphedema patients with grades 2 and 3 lymphedema. We believe that the final data indicate not only the size of the problem but also the impact of chronic edema on patient lives in terms of functionality and QoL. This will assist lymphedema services to provide evidence-based care. The Turkish LIMPRINT study results demonstrate that many patients cannot access treatment services because of the distance and cannot afford to pay for costly treatments as these are not completely reimbursed. We hope this evidence-based data will change the national policies for the care of Turkish patients with lymphedema or chronic edema.

Conclusion

This final LIMPRINT data reflect that upper extremity lymphedema is more common than lower extremity and the major cause is cancer treatment, predominantly breast cancer in the Turkish LIMPRINT. The most striking results are that the patients suffer for a long time, most of the patients have uncontrolled lymphedema mostly grade 2 and have not received any previous treatment before the study. Turkish patients had less wounds compared with other studies undertaken in the LIMPRINT study. This is most certainly because of the center characteristics that were rehabilitation services treating a high proportion of cancer patients, particularly breast cancer, rather than dermatology or vascular surgery services. The majority of patients had reduced functional status and decreased QoL. Although most of the patients had social health security for free complex decongestive therapy treatment, their ability to access these centers was more difficult than previously estimated. National health policies and planning are needed for the prevention, diagnosis, and treatment of those suffering this neglected condition in Turkish patients.

Author Disclosure Statement

No competing financial interests exist.

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