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Low Back Pain
Work-up
Physical examination.
Standing. Examine for obvious defects. Palpate for
tenderness or muscle spasm. Test the mobility of the lumbar spine with flexion,
extension, and lateral flexion. Observe the patient's gait and have the patient
walk on his toes (foot plantar flexion test S1) and up on his heels (foot
dorsiflexion test L5).
With the patient sitting. Sitting
straight-leg raising (SLR) test: passive extension of the knee. A positive
test is radicular pain at less than 60 degrees. 'Crossover' pain with
radicular symptoms in the leg not lifted is fairly specific for disk disease.
Reflexes. Patellar reflex tests the L4 root; Achilles
tendon reflex tests the S1 root (L5-S1 disk). Babinski sign: if present,
indicates disorder above the lumbar region such as cord tumor or CVA.
Sensation. L4: medial border of the feet; L5:
triangular area at the base of middle toes on the dorsum of the feet; S1:
lateral margin of the feet and distal portion of the calf.
Sensation. Check hip abduction (L5 motor), perianal
sensation (S3-5: also controls anal and urethral sphincter tone), hip extension
(L5 motor). Saddle anesthesia, decreased anal sphincter tone, and crossover leg
pain are signs of a central disk herniation, which is considered a surgical
emergency. Must be suspected if there is a history of new
bowel or bladder incontinence.
Laboratory and imaging studies.
Lumbar spine films are not necessary in most patients. Plain films should be obtained
if symptoms last more than 6 weeks, there is suspicion or history of
malignancy, or the patient is using steroids, is over 50 years of age, has a
history of trauma, or has neurologic deficits. There is no need to obtain
radiographic evaluation for history consistent with muscle strain.
Patients suspected of having infectious or neoplastic causes of low back pain
should have an imaging study such as a bone scan, CT, or MRI.
If severe symptoms persist for several weeks despite conservative therapy and
disk herniation or another surgically correctable disorder is suspected, then
CT or MRI imaging may be useful. Generally, since will not
want to intervene surgically unless pain is present for at least 6 weeks, no
need for these imaging studies unless there is some indication other than pain
(that is, neurologic symptoms such as loss of bowel and bladder function).
MRI and CT have replaced myelography except in rare circumstances.
Electromyogram and nerve conduction velocity. Can be used to evaluate suspected nerve root involvement.
Blood tests. Differential CBC with ESR, and
biochemical screening (calcium phosphate, alkaline phosphatase) should be
performed when a systemic cause for back pain is suspected.
Immunoelectrophoresis of serum and urine samples. Allows diagnosis of most cases of myeloma.
Treatment
Acute back pain (no longer than 6 weeks).
There is no difference in outcome when patients with acute back pain are
treated by a family physician, a chiropractor, or an orthopedic surgeon. Therapy
by a family physician is the most cost effective.
Regardless of the method of treatment, 40% better within 1 week, 60% to 85% in
3 weeks, and 90% in 2 months. Negative prognostic factors include more than 3
episodes of back pain, gradual onset of symptoms, and prolonged absence from
work.
Bed rest. Should be kept to a minimum, and early
mobilization encouraged. If symptoms recur or considerable pain develops in
relation to a specific activity or level of activity, the patient should
temporarily limit activity for several days but should not cease all activity.
Analgesia. NSAIDs most commonly used. Provide pain
relief and decrease inflammation. Acetaminophen provides analgesia but has no
anti-inflammatory properties. May be used with or instead of
NSAIDs. Narcotics should be used for short term only for severe pain.
Muscle relaxants such as cyclobenzaprine 10 mg PO TID
or QID work mostly by sedating patients and preventing activity. However, they
probably have little effect on muscle spasm.
Physical therapy. Although classically several modes
have been used to hasten resolution of back pain, most physical therapy modes
have no effect when rigorously tested. Traction, local application of heat,
cold, and ultrasound, and corsets have been shown to
have no effect. Transcutaneous nerve stimulation may provide short-term
symptomatic relief but have no proved long-term benefit.
Epidural steroid injections. May
speed recovery from radicular pain.
Rehabilitation exercises. Trunk extensors, abdominal muscles,
aerobic conditioning. Main benefit is that they promote early
mobilization, which is critical in treating acute back pain. The specific
exercise doesn't matter as much as the mobilization.
Chronic back pain. Once back pain has been established
for more than 1 year, the prognosis is poor. Mild analgesia should be used, avoidance of chronic or repeated reliance on narcotics
for pain control is a key management priority. If depression is encountered, it
should be treated.
Indications for admission and referral. Cauda equina
syndrome (urinary retention, sphincter incontinence, saddle
anesthesia), severe neurologic deficits (footdrop, gastrocnemius-soleus or
quadriceps weakness), progressive neurologic deficit, or multiple nerve root
involvement.
A 67-year-old white male retired factory worker
was found to have an abdominal aortic aneurysm on routine physical examination.
A vascular surgeon has recommended operative repair. The patient is a former
smoker, with a 10-pack-year smoking history. Three years ago, while under the
stress of a forced retirement, he had angina which responded well to sublingual
nitroglycerin. He has had no angina for 1 year.
Which one of the following conditions would be the most likely cause of
perioperative death in this patient?
a.Pulmonary complications
b.Peripheral embolization
c.Operative site infection
d.Myocardial infarction
e.Cerebral infarction
D
Myocardial infarction is the major cause of
perioperative death in patients undergoing surgery for abdominal aortic aneurysm.
This is especially true of patients with a history of known coronary artery
disease or with EKG abnormalities, and it is true even if the coronary artery
disease is stable.
Cerebral infarction occurs infrequently, even though cerebral vascular disease
is commonly present in this patient group. Operative site infection, peripheral
embolization, and pulmonary complications are all significant postoperative
complications which may cause death, but they are less frequent causes of death
than myocardial infarction.
A patient falls on his outstretched hand and
complains of pain in the wrist. There is tenderness to palpation over the
anatomic 'snuff box,' but multiple radiographs of the wrist are
negative.
The most appropriate treatment would be to
a.place
in a thumb spica cast for 3-4 months
b.place in a short-arm cast for 6-8 weeks
c.place in a long-arm cast for 4-6 weeks
d.immobilize with a plaster cast and obtain additional radiographs in 2 weeks
D
Since scaphoid fractures may not be evident on radiographs for 10 days to 2 weeks, sprains with tenderness over the scaphoid should be immobilized in a splint or cast for 2 weeks and then re-examined by x-ray. If a fracture is demonstrated, a thumb spica cast should be placed on the limb for 2-5 months, depending on which portion of the scaphoid is injured.
The mother of a newborn female who has
bilateral cleft lip and palate refuses to nurse her and asks the nurses to feed
her in the nursery rather than in her room.
Of the following, the MOST likely explanation for this response is
A. denial that the condition exists
B. fears over the baby's appearance
C. feelings of anger
D. feelings of guilt
E. mourning the loss of a normal child
A or C
A 56-year-old white male has cirrhosis which has
progressed as he has ignored your advice to stop drinking. You hospitalize him
for treatment of gastrointestinal bleeding. Gastroscopy shows the bleeding to
be due to gastritis rather than to an ulcer or varices. His bleeding is
stopped, plasma volume is restored with packed red cells, and he does not
develop delirium tremens. You administer spironolactone (Aldactone), and over
the course of a week in the hospital he loses approximately 10 kg of ascitic
fluid.
He is scheduled to be discharged tomorrow morning, but he suddenly develops
abdominal pain and a temperature of 38.9 C (102.0 F), and becomes delirious.
When you examine him, you find a blood pressure of 90/60 mm Hg, hypoactive
bowel sounds, and a diffusely tender abdomen with nonlocalized rebound
tenderness. An abdominal tap reveals cloudy ascitic fluid with a large number
of polymorphonuclear leukocytes.
The most likely cause of this sudden change in his condition is
a.spontaneous bacterial peritonitis
b.spontaneous pneumoperitoneum
c.a perforated diverticulum
d.a perforated gastric ulcer
e.acute pancreatitis
A
Spontaneous bacterial peritonitis is an
increasingly frequent complication of cirrhosis and other conditions which
cause ascites. This patient has a classic clinical presentation, with abdominal
pain, fever, rebound tenderness, hypoactive bowel sounds, hypotension, and
cloudy ascitic fluid. All of these findings are not invariably seen with this
condition, however.
Spontaneous bacterial peritonitis occurs in alcoholic cirrhosis, other types of
liver disease, occasionally in biliary cirrhosis and cardiac cirrhosis,
alcoholic hepatitis, and acute viral hepatitis. It is common in disseminated
lupus and can occur in children with nephrotic ascites. Multiple organisms may
be involved. The great majority of cases occur in hospitalized patients, and at
least 80% of patients have been hospitalized more than a week.
Diverticulitis, appendicitis, and a perforated gastric ulcer are much less
likely to produce the generalized abdominal tenderness with rebound seen in
peritonitis. Pancreatitis tends to be a presenting complaint rather than a
complication developing in a hospitalized patient. Spontaneous pneumoperitoneum
is not a frequent complication in patients without extensive diverticulitis.
A 60-year-old white male has had intermittent
posterior nuchal headaches for many years. Which one of the following is most
likely to help establish a diagnosis?
a.An MRI scan of the head
b.A CT scan of the head
c.An erythrocyte sedimentation rate
d.A neurologic examination
e.A thorough history
E
The best information for making the diagnosis in the patient presented is most likely to come from a thorough history focusing on provocation, quality, region, strength, and timing of the headaches, as well as associated symptoms, a medication history, and screening for depression. CT and MRI scans have not been proven helpful if focal clues are not found. Laboratory tests are not generally helpful when used randomly. While a complete neurologic examination should be done, the results are usually normal in patients with chronic headaches
A 25-year-old white male complains of the recent
onset of rapidly progressing periodontitis. As part of your evaluation, which
one of the following tests would be most advisable?
a. Serum lead
b. Serum ferritin
c. Serum B12
d. HIV titer
D
Rapidly progressive periodontitis appears to be an early sign of immunocompromise in patients with HIV infection. HIV antibody titers and T4:T8 lymphocyte ratios are indicated, especially if the patient's dental hygiene appears adequate. Dental referral is also indicated. None of the other tests mentioned is associated with periodontitis.
A 29-year-old white female is hospitalized
following a right middle cerebral artery stroke confirmed on an MRI scan. Her
past medical history is remarkable only for a history of an uncomplicated
tonsillectomy during childhood, and a second-trimester miscarriage 3 years ago.
The only remarkable finding on physical examination is left hemiplegia.
The initial laboratory workup reveals normal hematocrit and hemoglobin levels,
a normal prothrombin time, and a platelet count of 200,000/mm3 (N
140,000-440,000). The active partial thromboplastin time is 95 sec (N
23.6-34.6), and it does not normalize when the patient's serum is mixed with
normal plasma. A serum VDRL is positive, and a serum FTA-ABS is nonreactive.
Which one of the following is the most likely diagnosis?
a. Protein C deficiency
b. Thrombotic thrombocytopenic purpura
c. Antiphospholipid syndrome
d. Neurosyphilis
e. Hemophilia
C
The antiphospholipid syndrome occurs because of
the appearance of a heterogeneous group of circulating antibodies to negatively
charged phospholipids, including most commonly a lupus anticoagulant and
anticardiolipin antibodies. The antibodies are usually detected by a
false-positive serologic test for syphilis. Clinical features include venous
and arterial thrombosis, fetal wastage, thrombocytopenia, and the presence of
an activated partial thromboplastin time inhibitor. It is an important
diagnostic consideration in all patients with unexplained thrombosis or
cerebral infarction, particularly in young patients.
Although hemophilia would also be associated with a prolonged activated partial
thromboplastin time (aPTT), the PTT would normalize when the patient's serum
was mixed with normal plasma. Neurosyphilis is excluded by the negative serum
FTA-ABS result. Thrombotic thrombocytopenic purpura is not associated with
prolongation of the aPTT and is associated with a hemolytic anemia. Although
protein C deficiency is a hypercoagulable state that can lead to stroke, none
of the laboratory abnormalities suggests this diagnosis.
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