The purposes of this study are * to determine the prevalence, size and impact on quality of life of lymphedema of the lower extremities after primary radical surgery with hysterectomy +/- pelvic - and paraaortic lymphadenectomy in women with endometrial uterine carcinoma FIGO (International Federation of Gynecology and Obstetrics) stage 1 and 2 * to analyze risk factors for development of lymphedema in this specific group of patients. Our hypotheses are that women who have lymphadenectomy more often suffer from lymphedema, subjectively and objectively, and have an impaired quality of life. This is a Swedish multicenter study carried out in 17 departments of Obstetrics and Gynecology and in 3 departments of Oncology. All participants are treated according to the Swedish National Guidelines for Endometrial Cancer. 130 women with endometrial cancer who have a hysterectomy with lymphadenectomy (high-risk endometrial carcinomas) and 130 women with endometrial cancer who have a hysterectomy without lymphadenectomy (low-risk endometrial carcinomas) are prospectively enrolled in the study. The participants are examined preoperatively and on 3 occasions postoperatively, i.e. 4-6 weeks , 6 months and 12 months postoperatively. Determination of occurrence of lymphedema of the lower extremities are determined objectively by 1) a standardized clinical evaluation according to Bruna et al.\[1\] and 2) determining the leg volume according to the cone model by Sitzia \[2\] by systematically measuring of leg circumferences. In addition, occurrence of lymphedema is measured subjectively by the participants. On the same four occasions as the leg circumference measurements are conducted the patients complete two generic health related quality of life forms (the EuroQol EQ-5D and the Short-Form 36 SF-36) and the condition specific quality of life form for limb lymphedema (LYMQOL). Demographic and clinical data are systematically collected until one year postoperatively including occurrence of complications and given adjuvant oncological therapy such as chemo- and radiation therapy. On each occasion of clinical control a vaginal ultrasound examination is carried out in order to register pelvic and abdominal lymphocele formation or lymphatic fluid effusion intraabdominally.
Not included
Study Type
OBSERVATIONAL
Enrollment
262
Pelvic and/or paraaortic lymphadenectomy
Highland hospital
Eksjö, Jonkopings Län, Sweden
Falu Central Hospital
Falun, Sweden
Gävle County Hospital
Gävle, Sweden
Sahlgrenska University Hospital
Gothenburg, Sweden
Region Halland Halmstad Hospital
Halmstad, Sweden
County Hospital in Kalmar
Kalmar, Sweden
Blekinge Hospital
Karlskrona, Sweden
Karlstad Central Hospital
Karlstad, Sweden
Linkoping University Hospital
Linköping, Sweden
Södra Älvborgs Sjukhus
Skövde, Sweden
...and 6 more locations
Change in leg volume from baseline (preoperatively) to 4-6 weeks postoperatively
Leg volume is determined by the cone model according to Sitzia by measuring leg circumferences systematically.
Time frame: 4-6 weeks after the primary surgery
Change in leg volume from baseline (preoperatively) to 6 months postoperatively
Leg volume is determined by the cone model according to Sitzia by measuring leg circumferences systematically.
Time frame: 6 months after the primary surgery
Change in leg volume from baseline (preoperatively) to 12 months postoperatively
Leg volume is determined by the cone model according to Sitzia by measuring leg circumferences systematically.
Time frame: 12 months after the primary surgery
Change in quality of life assessment from baseline (preoperatively) to 4-6 weeks postoperatively
Quality of life measured by means of The EuroQol (EQ-5D), the Short-Form 36 (SF-36) and the condition specific quality of life form LYMQOL.
Time frame: 4-6 weeks from the primary surgery
Change in quality of life assessment from baseline (preoperatively) to 6 months postoperatively
Quality of life measured by means of The EuroQol (EQ-5D), the Short-Form 36 (SF-36) and the condition specific quality of life form LYMQOL.
Time frame: 6 months from the primary surgery
Change in quality of life assessment from baseline (preoperatively) to 12 months postoperatively
Quality of life measured by means of The EuroQol (EQ-5D), the Short-Form 36 (SF-36) and the condition specific quality of life form LYMQOL.
Time frame: 12 months from the primary surgery
Percentage of participants with an increase in leg volume of > 15% 12 months postoperatively
Time frame: 12 months after the primary surgery
Percentage of participants who states they have lymphedema
Occurrence of lymphedema subjectively graded as 2 or more on an ordinal scale from 1 to 4. 1 express no swelling of the legs and 4 express severe swelling.
Time frame: 12 months from the primary surgery
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