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Patient-controlled
analgesia (PCA) is a widely used method for controlling
pain in settings ranging from surgical floors to obstetrical
units and intensive care. As PCA therapy becomes more
commonplace the possibility of decreased vigilance on
the part of the caregivers to monitor for complications
becomes possible. Patient-controlled analgesia is viewed
as a safe and effective method for administering medication
for short-term relief of pain. However, there are complications
associated with its use. These range from programming
errors to nausea and vomiting to respiratory depression.
Now may be an appropriate time to revisit monitoring guidelines
for the use of PCA devices.
Patient-controlled
analgesia is usually administered by IV or epidural routes.
Pain medication is given as a small continuous (basal)
rate with bolus infusions when the patient pushes a button.
This allows the patient to have nearly continuous pain
control without the peak and valley effects associated
with IM and oral administration. Patient-controlled analgesia
works well to control short-term pain such as that experienced
after surgery and during painful procedures. It has gained
popularity with patients, because they have a feeling
of control over their pain relief. In fact, many patients
are asking their doctors to prescribe it.
The
setup for IV or epidural administration of PCA is the
same. A special syringe is filled with a pre-determined
concentration of medication, usually morphine or Demerol.
The syringe is inserted into a special PCA pump that controls
the rate of the infusion and calculates the amount of
time between patient-requested doses. The PCA pump can
be set to prevent an overdose by controlling the number
of doses, and hence the amount of medication. Pain medication
requirements differ among patients, therefore the nurse
and doctor must determine the optimal dose for each patient
and program it into the pump.
PCA
pumps are designed to accept a variety of medications
and drug concentrations. Complications can occur due to
errors in programming the PCA pump. Therefore, the nurse
initiating therapy must program the pump to deliver the
prescribed dosage based on the drug concentration. Incorrect
drug concentrations, incorrect rates, and calculation
errors can lead to inaccurate drug delivery. Factors associated
with programming errors include inexperienced or poorly
trained nurses, mathematical errors, and a user interface
that is difficult to use (Eade, D.M., 1997). Better training
with competency reviews could help reduce errors from
training deficiency.
Pain
management centers often use larger doses of narcotics
to treat pain. In fact, some experts believe that there
is no upper limit on the dosage of morphine sulfate in
the patient with intractable pain. In addition, many practitioners
are using high dose narcotics along with potentiating
agents, such as Phenergan or combination therapy with
non-narcotic pain medicines, such as Toradol.
Giving
pain medications can lead to unwanted complications. The
more severe complications are respiratory depression,
respiratory arrest, and allergic reaction. These can be
life threatening and require a high level of observation
to prevent. Less severe complications include nausea,
vomiting, constipation, and increased somnolence. The
combination of respiratory depression and neurological
depression can make the patient at risk for atelectasis,
pulmonary edema, and acute respiratory distress syndrome
(ARDS).
Some
strategies to prevent complications include closely monitoring
the patient's response to changes in dosage. Respiratory
depression can be a fatal complication of narcotic administration,
and is caused by narcotic depression of the central nervous
system. Sedation from narcotics can lead to decreased
respiratory effort and cause atelectasis. Respiratory
or neurological depression should be monitored closely
in any patient receiving PCA. Pulmonary interventions
such as coughing, deep breathing, forced expiration, and
incentive spirometry should be implemented hourly to prevent
respiratory complications. An interface or connection
to an apnea monitor or pulse oximetry monitor could alert
the nurse of impending respiratory depression.
The
narcotics used in PCA pumps can cause nausea and vomiting.
One study (Snell, et al.) found that patients taking intramuscular
pain medications used three times as much antiemetics
as the PCA group. However, this may be due to arbitrary
pre-mixture with narcotics by nurses. Complaints of nausea
should be taken seriously, especially in post-operative
patients who are at risk for aspiration due to the residual
effects of anesthesia. Aspiration of stomach acid can
cause pneumonitis and acute respiratory distress syndrome.
Hourly
monitoring of patient status may be necessary if the patient's
response to narcotic is unknown, and after changing the
type of medication or dosage. Increased observation should
be exercised with patients receiving multiple pain medications.
Lastly, reversing agents such as Narcan for narcotics,
and Rumazican for benzodiazepam should be readily available
for use if oversedation or respiratory depression occurs.
In
conclusion, PCA pumps provide valuable relief for short-term
pain. However, their use can be associated with respiratory
depression and other complications, especially at higher
doses. Individualized therapy and close monitoring are
essential to provide for patient safety. Hospitals should
have clearly defined protocols for the administration
of PCA and monitoring for side effects to prevent untoward
patient outcomes.
Resources:
Intravenous
Nurses Society
Pain dot com
Nursing
Continuing Education
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