The patient who feels pain can best assess the degree of its relief, a
nd therefore the effective pharmacological treatment of pain requires
the active participation of the patient, patient-controlled analgesia
(PCA) involves the patient in a direct manner; the patient is given co
ntrol over at least some aspects (usually the timing of doses) of anal
gesic drug administration. A wide range of therapeutic strategies fall
under the umbrella of PCA. In one major area of application, the cont
rol of severe acute pain such as postoperative pain, the term PCA is u
sed to describe a specific type of treatment. This involves a device c
onsisting of a pump, containing a reservoir of drug, and a handset tha
t administers a dose of drug when activated by the patient. Such a sys
tem was first used by Sechzer over 20 years ago. Today, the device may
be a microprocessor-controlled system, able to implement complex inst
ructions programmed by the prescriber and keep a record of the patient
-device interactions, or it may he a simple disposable pump powered by
mechanical means such as a spring or an elastomeric drug reservoir. T
he usual route of PCA drug administration after surgery is intravenous
, but others, particularly the epidural route, are also used. The most
commonly used drugs are opioid mu-receptor agonists such as morphine
and fentanyl. While many such agents have been used, the differences b
etween them in terms of efficacy and adverse effects are modest. When
administering analgesics by PCA the prescriber can choose the drug to
be used and the size of each dose to be administered, and can impose c
ertain constraints on drug administration. The most common constraint
is a lockout interval, a period following the administration of a dose
during which the device will not administer a second dose, even thoug
h the patient activates the handset. Within the constraints, the patie
nt controls when doses of the drug are administered, Variants of PCA i
nclude the addition of a background infusion of the drug, which may va
ry or be constant, providing the patient with control over the size an
d timing of doses, and the addition of other drugs, such as antiemetic
s, to the drug reservoir. In practice, a standard PCA prescription wil
l be used at a particular hospital (e.g. drug: morphine sulphate, dema
nd dose: 1 mg, lockout interval: 5 minutes, background infusion: none)
, Although PCA is well accepted by most patients, simply initiating PC
A does not guarantee good pain control. Patients must be selected appr
opriately, and educated preoperatively in the effective use of PCA. Th
is information should be reinforced by nursing staff during the postop
erative period. Pain control and adverse effects need to be monitored
regularly, and the prescriber must be prepared to change the prescript
ion (e.g., dose size or lockout interval) to meet the individual needs
of the patient. Extensive experience with intravenous PCA has shown t
he risk of serious adverse events to be low. The risk is increased mea
surably when the patient's degree of control over drug administration
is reduced, such as when a background infusion is added, and additiona
l monitoring may then be required to maintain the level of safety. Exp
erience with epidural PCA is more limited but, whilst there are additi
onal risks, it is still relatively well tolerated. Although modern PCA
devices are very reliable, there are a number of reports every year o
f patients put at risk by mistakes made by staff when initiating PCA,
The direct cost of providing postoperative analgesia by PCA is greater
than that of traditional approaches such as nurse-administered intram
uscular injection of analgesics. However. given the good efficacy and
excellent patient satisfaction, the benefits of PCA outweigh the small
additional costs.