Lymphedema Case Study J.D.
Healthtronix Lymphedema Treatment Center
Susie Wills, BSN, RN, CLT
Director of Clinical Services
SOC--9/7/99
Discharge--9/23/99
PATIENT INFORMATION: Ms. J.D. is a 56 y/o female who has lymphedema in
her (L) upper extremity secondary to a lumpectomy of her (L) breast with lymph
node dissection followed by radiation therapy. She states that her
lymphedema began immediately after her surgery. She denied ever having
cellulitis in her affected arm.
PREVIOUS TREATMENT: She has in the past used a compression pump and
compression sleeve; however, she admitted that she did not use any of
these on a routine basis and had not used her compression pump in months.
EXACERBATION: The patient reported that she had a significant increase in
the edema in her (L) arm which she attributed to the summer heat. The
neurological symptoms had increased in her arm. She stated that on a
scale of 1 to 10 with 10 being unbearable that heavy, tired and aches were 9/10.
The quality of her life was decreased due to the pain, fatigue and loss of
function of her arm. The weight of her (L) arm was also affecting her
posture and spinal alignment.
OBSERVATION: The (L) arm was visibly larger than the (R). Her (L)
forearm appeared to be 2X the size of her (R) forearm. There was a deep fold at
the (L) wrist with edematous tissue covering the wrist and part of the hand.
The arm went in at the elbow; however, it protruded anteriorly and
posteriorly at the upper arm and there was a bluish-red discoloration on
the anterior upper arm. After measuring the circumference of both arms at 4
cm. intervals, the edema volume chart revealed that the volume her (L) arm was
42.7% greater than that of her (R) unaffected arm. This was approximately
2,820 ml. of excess fluid.
TREATMENT: Her treatment plan consisted of MLD/CDP daily X 20 treatments,
an Optiflow SC insert to be worn under the Lymphapress 201M pump that she
already owned, the Reid Sleeve to be worn at bedtime and a custom fitted
Juzo compression sleeve and gauntlet to be worn during the waking hours.
She was also instructed in arm and breathing exercises, precautions, skin
care, nutrition, and self MLD.
RESULTS: The patient responded almost immediately to her therapy. On
9/13/99, after 3 MLD/CDP treatments she was again measured and her edema
volume chart showed an 84% reduction of the fluid which approximated 2,368
ml. of fluid. After 7 MLD/CDP treatments, the patient was again measured
and this revealed a 94.4% reduction of fluid (2,662 ml.) The patient
reported that her neurological symptoms had been diminished greatly and
that she could actually see her (L) wrist for the first time in years. At this
time, the patient opted to discontinue her MLD due to her out of pocket
expense. Her home equipment was set-up with her, so that she could
continue her treatment at home.
HOME PROGRAM: The patient was discharged with a printed instruction
sheet covering all aspects of her home maintenance program. (See attached)
FOLLOW UP: The patient is to return in 4-6 months for a new compression
sleeve and gauntlet. She also has orders for further MLD should she need
it. She was encouraged to attend a lymphedema support group in her area.
She is continuing her career as a pre-school director.