DATE: August 25, 2009
Patient: XXXXXXXX
DOB: XXXXXXXX
Physician/NP/PA: XXXXXXXX,
M.D.
HISTORY: Patient is a 49-year-old
female with known chronic refractory neck and low back pain. At the present time, she is here for
obtaining diagnostic facet joint injection block/interventional management for
her low back pain. She relates some
additional pain discomfort in her bilateral hip greater trochanteric area.
Interval history
intake updates completed, reviewed, and documented in EMR.
The following interventional procedure
was carried out at Pain Clinic fluoroscopy suite after discussing risks,
benefits, alternatives and complications to procedure.
PROCEDURE:
Bilateral L3/4, L4/5, and L5/S1
facet/zygapophysial joint injection/block with fluoroscopy.
PRE & POST PROCEDURE DIAGNOSIS:
Lumbosacral spondylosis/lumbar facet
syndrome/chronic refractory low back pain.
Relevant
pre-procedure assessment carried out. Integument
corresponding to area examined negative for any active infection. Vitals’
monitored and patient confirmed stable prior to proceeding with procedure.
Patient positioned prone, vertebrae squared, oblique or Scottie dog view
obtained, skin marked corresponding to lower pole of above facet joints. Area swabbed with Betadine and sterile
draped. 25G Quincke point spinal needles
introduced and advanced to above facet joints down the barrel. Intraarticular
placement achieved with feel of needle entry.
Small volume of Isoview-200, 0.25ml injected to additionally
confirm intraarticular-intracapsular localization of contrast. Confirming negative aspiration for heme 10 mg
of Kenalog with 0.5 ml of 0.5% Marcaine injected into each facet joint. Needle withdrawn, hemostasis confirmed.
Patient
tolerated procedure well. No
complications encountered, no blood loss assessed. Stable clinical condition confirmed post
procedure. Safety with
ambulation/mobility assessed prior to discharge. Post-procedure care and discharge
instructions reviewed and a written copy given to patient.
Note: Additional
history intake, interval history updates, procedure specific informed consent,
pre and post-procedure assessment, post-procedure care and discharge
instructions documented in patient’s chart, please refer to.
“Procedure
Concordant Pain Relief Report Form” initiated and patient instructed to monitor
and mark degree of pain relief on a numeric pain scale ranging from 0 – 10 over
the next 24 hours.
If patient
obtains significant relief of usual back pain with above intervention will
follow‑up with repeat facet block to evaluate candidacy for radiofrequency
ablation of the same joints.
Sincerely,
___________________________
XXXXXXXX,
M.D.
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