In: Anatomy and Physiology
Consult - History and Physical
Lumbosacral Polyradiculopathy
Description: Briefly, the patient has a
lumbosacral polyradiculopathy that is temporally related to the
epidural anesthesia given to her in October of 2017.
HISTORY OF PRESENT ILLNESS: The patient is a
35-year-old woman who reports that on the 30th of October 2017, she
had a rupture of her membranes at nine months of pregnancy, and was
admitted to hospital and was given an epidural anesthetic. I do not
have the records from this hospital admission, but apparently the
epidural was administered for approximately 14 to 18 hours. She was
sitting up during the epidural.
She did not notice any difference in her lower extremities at the
time she had the epidural; however, she reports that she was
extremely sleepy and may not have been aware of any change in
strength or sensation in her lower extremities at that time. She
delivered on the 31st of October, by Cesarean section, because she
had failed to progress and had pyrexia.
She also had a Foley catheter placed at that time. On the 1st of
November 2017, they began to mobilize her and it was at that time
that she first noticed that she could not walk. She was aware that
she could not move her legs at all, and then within a few days, she
was aware that she could move toes in the left foot but could not
move her right foot at all. Since that time, there has been a
gradual improvement in strength to the point that she now has
limited movement in her left leg and severely restricted movement
in her right leg. She is not able to walk by herself, and needs
assistance to stand. She was discharged from hospital after the
Cesarean section on the 3rd of November. Unfortunately, we do not
have the records and we do not know what the discussion was between
the anesthesiologist and the patient at the time of discharge. She
was then seen at Avery Hospital on November 05, 2017. She had an
MRI scan of her spine, which showed no evidence of an abnormality,
specifically there were no cord changes and no evidence of a
hematoma. She also had an EMG study at that time by Dr. Xavier,
which was abnormal but not diagnostic and this was repeated again
in December. At the present time, she also complains of a pressure
in both her legs and in her thighs. She complains that her right
foot hurts and that she has some hyperesthesia there. She has been
taking gabapentin to try to reduce the discomfort, although she is
on a very low dose and the effect is minimal. She has no symptoms
in her arms, her bowel and bladder function is normal, and her
bulbar function is normal. There is no problem with her vision,
swallowing, or respiratory function.
PAST MEDICAL HISTORY: Unremarkable except as noted
above. She has seasonal allergies.
CURRENT MEDICATIONS: Gabapentin 300 mg b.i.d.,
Centrum once a day, and another multivitamin.
ALLERGIES: She has no medication allergies, but
does have seasonal allergies.
FAMILY HISTORY: There is a family history of
diabetes and hypertension. There is no family history of a
neuropathy or other neurological disease. She has one child, a son,
born on October 31, 2017.
SOCIAL HISTORY: The patient is a civil engineer,
who currently works from home. She is working approximately half
time because of limitations imposed on her by her disability, need
to attend frequent physical therapy, and also the needs of looking
after her baby. She does not smoke and does not drink and has never
done either.
GENERAL PHYSICAL EXAMINATION:
VITAL SIGNS: P 74, BP 144/75, and a pain score of 0.
GENERAL: Her general physical examination was unremarkable.
CARDIOVASCULAR: Normal first and second heart sound, regular pulse
with normal volume.
RESPIRATORY: Unremarkable, both lung bases were clear, and
respiration was normal.
GI: Unremarkable, with no organomegaly and normal bowel
sounds.
NEUROLOGICAL EXAM:
MSE: The patient's orientation was normal, fund of knowledge was
normal, memory was normal, speech was normal, calculation was
normal, and immediate and long-term recall was normal. Executive
function was normal.
CRANIAL NERVES: The cranial nerve examination II through XII was
unremarkable. Both disks were normal, with normal retina. Pupils
were equal and reactive to light. Eye movements were full. Facial
sensation and strength was normal. Bulbar function was normal. The
trapezius had normal strength.
MOTOR: Muscle tone showed a slight increase in tone in the lower
extremities, with normal tone in the upper extremities. Muscle
strength was 5/5 in all muscle groups in the upper extremities. In
the lower extremities, the hip flexors were 1/5 bilaterally, hip
extensors were 1/5 bilaterally, knee extension on the right was 1/5
and on the left was 3-/5, knee flexion was 2/5 on the right and
3-/5 on the left, foot dorsiflexion was 0/5 on the right and 1/5 on
the left, foot plantar flexion was 4-/5 on the right and 4+/5 on
the left, toe extension was 0/5 on the right and 4-/5 on the left,
toe flexion was 4-/5 on the right and 4+/5 on the left.
REFLEXES: Reflexes in the upper extremities were 2+ bilaterally. In
the lower extremities, they were 0 bilaterally at the knee and
ankles. The abdominal reflexes were present above the umbilicus and
absent below the umbilicus. The plantar responses were mute. The
jaw reflex was normal.
SENSATION: Vibration was moderately decreased in the right great
toe and was mildly decreased in the left great toe. There was a
sensory level to light touch at approximately T7 posteriorly and
approximately T9 anteriorly. There was a range of sensation, but
clearly there was a decrease in sensation below this level but not
complete loss of sensation. To pain, the sensory level is even less
clear, but appeared to be at about T7 on the right side. In the
lower extremities, there was a slight decrease in pin and light
touch in the right great toe compared to the left. There was no
evidence of allodynia or hyperesthesia. Joint position sense was
mildly reduced in the right toe and normal on the left.
COORDINATION: Coordination for rapid alternating movements and
finger-to-nose testing was normal. Coordination could not be tested
in the lower extremities.
GAIT: The patient was unable to stand and therefore we were unable
to test gait or Romberg's. There was no evidence of focal back
tenderness.
REVIEW OF OUTSIDE RECORDS: I have reviewed the
records from Avery Hospital, including the letter from Dr. Yansen
and the EMG report dated 12/17/2017 from Dr. Xavier. The EMG report
shows evidence of a lumbosacral polyradiculopathy below
approximately T6. The lower extremity sensory responses are
essentially normal; however, there is a decrease in the amplitude
of the motor responses with minimal changes in latency. I do have
the MRI of lumbar spine report from 11/06/2017 with and without
contrast. This showed a minimal concentric disc bulge of L4-L5
without disc herniation, but was otherwise unremarkable. The
patient brought a disc with a most recent MRI study; however, we
were unable to open this on our computers. The verbal report is
that the study was unremarkable except for some gadolinium
enhancement in the lumbar nerve roots. A Doppler of the lower
extremities showed no evidence of deep venous thrombosis in either
lower extremity. Chest x-ray showed some scoliosis on the lumbar
spine, curve to the left, but no evidence of other abnormalities. A
CT pelvis study performed on November 07, 2017 showed some
nonspecific fluid in the subcutaneous fat of the back, posterior to
L4 and L5 levels; however, there were no pelvic masses or other
abnormalities. We were able to obtain an update of the report from
the MRI of the lumbar spine with and without contrast dated
12/30/2017. The complete study included the cervical, thoracic, and
lumbar spine. There was diffuse enhancement of the nerve roots of
the cauda equina that had increased in enhancement since prior exam
in November. It was also reported that the patient was given
intravenous methylprednisolone and this had had no effect on
strength in her lower extremities.
IMPRESSION: The patient has a condition that is
temporally related to the epidural injection she was given at the
end of October 2017, prior to her Cesarean section. It appears she
became aware of weakness within two days of the administration of
the epidural, she was very tired during the epidural and may have
missed some change in her neurological function. She was severely
weak in both lower extremities, slightly worse on the right than
the left. There has been some interval improvement in her strength
since the beginning of November 2017. Her EMG study from the end of
December is most consistent with a lumbosacral polyradiculopathy.
The MRI findings of gadolinium enhancement in the lumbar nerve
roots would be most consistent with an inflammatory radiculitis
most likely related to the epidural anesthesia or administration of
the epidural. There had been no response to IV methylprednisolone
given to her at Avery. The issue of having a lumbar puncture to
look for evidence of inflammatory cells or an elevated protein had
been discussed with her at both Avery and by myself. The patient
did not wish to consider a lumbar puncture because of concerns that
this might worsen her condition. At the present time, she is able
to stand with aid but is unable to walk. There is no evidence on
her previous EMG of a demyelinating neuropathy.
RECOMMENDATIONS:
The diagnostic issues were discussed with the patient at length.
She is informed that this is still early in the course of the
problem and that we expect her to show some improvement in her
function over the next one to two years, although it is unclear as
to how much function she will regain.
She is strongly recommended to continue with vigorous physical
therapy, and to continue with the plan to mobilize her as much as
possible, with the goal of trying to get her ambulatory. If she is
able to walk, she will need bilateral AFOs for her ankles, to
improve her overall mobility. I am not prescribing these because at
the present time she does not need them.
We discussed increasing the dose of gabapentin. The paresthesias
that she has may indicate that she is actually regaining some
sensory function, although there is a concern that as recovery
continues, she may be left with significant neuropathic pain. If
this is the case, I have advised her to increase her gabapentin
dose from 300 mg b.i.d. gradually up to 300 mg four times a day and
then to 600 mg to 900 mg four times a day. She may need other
neuropathic pain medications as needed. She will determine whether
her current symptoms are significant enough to require this
increase in dosage.
The patient will follow up with Dr. Yansen and his team at Avery
Hospital. She will also continue with physical therapy within the
Avery system.
Questions (One to two pages, please):
1. In a paragraph or two, write a complete explanation to the patient and her family, in lay terms, telling them what has happened and what the likely outcome will be.
The case study shows 35yr old lady affected by injury to nerves of lower spine area as a complication of epidural anesthesia given to her during her cesarian session. During the anesthesia, may be the needle hitted her nerves supplying lower body , which caused injury to nerves ,and leaded to loss of motor function and sensory function. It is the rate complication of anesthesia. The characteristics of injury includes increased sensation of pain, loss of electrical signals to the brain and sensation deficits of lower limb also.
She is improving day by day , in terms of motor function and sensory function. Physiotherapy is very important for improving the mobility of lower limbs. To make her ambulatory, it's better to implement motor learning exercises and neurodevelopmental exercises along with application of external appliances to lower body which aid in walking. Her outcome will be good regaining the lower body functions and will be able to walk , maximum improvement should occur within 6-9 months , after that Percentage of improvement will be less.