ffective postoperative pain
control is an essential component of the care of the
surgical patient. Inadequate pain control, apart from
being inhumane, may result in increased morbidity or
mortality (1, 2). Evidence suggests that surgery
suppresses the immune system and that this suppression is
proportionate to the invasiveness of the surgery (3, 4).
Good analgesia can reduce this deleterious effect. Data
available indicate that afferent neural blockade with
local anesthetics is the most effective analgesic
technique. Next in order of effectiveness are high-dose
opioids, epidural opioids and clonidine,
patient-controlled opioid therapy, and nonsteroidal
anti-inflammatory agents (5).
The advantages of
effective postoperative pain management include patient
comfort and therefore satisfaction, earlier mobilization,
fewer pulmonary and cardiac complications, a reduced risk
of deep vein thrombosis, faster recovery with less
likelihood of the development of neuropathic pain, and
reduced cost of care.
The failure to provide good postoperative analgesia is
multifactorial. Insufficient education, fear of
complications associated with analgesic drugs, poor pain
assessment, and inadequate staffing are among its causes.
ASSESSMENT
A proper approach to acute postoperative pain
management must include an appropriate assessment tool. A
10-point pain assessment scale, where 1 is no pain and 10
is the worst possible pain imaginable, has been
nationally accepted. The rating given to the patient's
pain depends on the observer. If a patient puts on a good
face when the attending physician makes rounds, a low
score may be given, when in fact a higher score would
have resulted if the patient was carefully questioned
after the physician left. Therefore, the assessment of
pain requires not only a subjective report by the patient
but also an objective observation by a pain therapist.
The influence of the pain therapy on clinical
function--such as the ability to take a deep breath,
cough, and move--can be ascertained. An important part of
the evaluation is a documented follow-up assessment to
note the efficacy of the therapy and the patient's
satisfaction with it.
The natural history of the pain should be understood,
so that therapy can be adjusted when needs change. The
source of the pain, as well as its severity, should be
noted. Pain symptoms that are inappropriate in site or
severity should be investigated for a potential
confounding pathology. Anxiety, fear, and cultural
influences should be understood and either treated or
accommodated as necessary.
The goal of pain management must be determined with
each patient. The goal may not be a score of 1; the
patient may be satisfied and functional with a score of
3, preferring to manage some pain and thereby avoid
unpleasant side effects of therapy, such as sedation,
nausea, or pruritus. The key is to reassess the patient
and determine if he or she is satisfied with the outcome.
A satisfaction score should be obtained together with a
pain score. This combination will help ensure that
unrelieved, unwanted pain does not go unnoticed.
Responsive analgesia management with good patient
communication is the key to a successful program.
SIDE EFFECTS
The goal of postoperative pain management is to
relieve pain while keeping side effects to a minimum.
After hundreds of years of advances, the mainstay of pain
therapy is still the opioids. While they are very
effective analgesics, opioids also carry
with them many undesirable side effects: sedation,
respiratory depression, nausea and vomiting, hypotension
and bradycardia, pruritus, and inhibition of bowel
function. The treatment of complications such as nausea
and pruritus may include the administration of
antihistamines, which have an additive effect on sedation
and respiratory depression.
Respiratory depression is the major life-threatening
complication of opioids. The incidence of severe
respiratory depression with patient-controlled analgesia
pumps has been reported to be as high as 1 per 10,000
patients. These events are usually associated with an
error in management (6, 7).
No highly sensitive instrument is available to monitor
respiratory depression in the extubated patient. The
pulse oximeter may be used to monitor respiratory
depression in the postanesthesia recovery unit or on the
ward when continuous infusions of narcotics are being
given, but pitfalls are associated with its use. The
pulse oximeter is a poor measure of hypoventilation when
the concentration of inspired oxygen is high (8). Since
many postoperative patients receive added oxygen, the
pulse oximeter detects respiratory depression very late.
The additional oxygen maintains the oxygen saturation
while the arterial carbon dioxide pressure may rise to
>100 mm Hg.
End-tidal carbon dioxide monitoring in the extubated
patient is also not very accurate. It depends on adequate
ventilation and air movement so that the carbon dioxide
level in the nose or mouth reflects that in the alveoli.
Depressed ventilation results in paradoxical breathing
and little air movement; therefore, the end-tidal carbon
dioxide concentration may be artificially low (9).
Respiratory rate measurement also correlates poorly with
respiratory depression.
The only noninvasive and readily available monitors of
respiratory depression are the observation of paradoxical
breathing and the level of consciousness or sedation of
the patient. Therefore, respiratory pattern and sedation
score should be documented in the charts of patients on
opiates.
SEDATION SCORES
Many groups have strongly recommended recording pain
measurement as the fifth vital sign on the patient's
chart. I believe that concomitant with this should be a
sixth vital sign, a sedation score. This is a matter of
patient safety, as respiratory depression resulting from
sedation and narcotic use is insidious and can very
easily occur unnoticed, with potentially disastrous
results. Sedation scores test the arousability of the
patient and can help prevent oversedation. More than 30
sedation scores have been published, all with certain
advantages or disadvantages. The first was published
>25 years ago and is accepted internationally as the
gold standard (Table) (10, 11). There are 3
important components of a sedation scoring system: it
should cause minimal disturbance to the patient, be
simple to use, and be part of routine assessment of the
patient.

THERAPEUTIC MODELS
Systemic opioids
Opioids act as agonists on central and peripheral
opioid receptors. They may be administered by many
different routes: oral, rectal, sublingual, transdermal,
subcutaneous, intramuscular, intravenous, or neuroaxial.
The intramuscular route is very often prescribed;
however, it is an unpredictable delivery system because
of wide swings in drug concentration. Therefore, it
requires careful reassessment of the patient. Intravenous
infusion administration results in a more constant blood
level.
The drugs commonly used are morphine, meperidine,
fentanyl, and hydromorphone. All of the narcotics, with
the exception of remifentanil, have active metabolites
that can result in an enhanced effect with impaired
excretion or prolonged use. The metabolites of meperidine
may cause seizures as they accumulate, and in the elderly
patient, meperidine may cause psychosis or delerium as a
result of its atropine-like effect on the central nervous
system.
Patient-controlled analgesia is used widely for the
management of postoperative pain. The advantages of this
modality are that the patient can obtain pain relief
without waiting for a caregiver, no painful injections
are required, and the patient retains a certain amount of
control (12). The safety of this system depends on the
proper functioning of the pump and its use by the patient
alone, not someone else such as a well-meaning family
member. The patient has to be conscious to activate the
system. If a continuous infusion mode is used, a better
level of analgesia may be provided, but the safety factor
may be lost. In this mode, it would be prudent to
carefully reassess the patient with a sedation score.
Oral opioids can be very effective and can be used to
rapidly wean a patient off parenteral therapy, thereby
allowing earlier discharge from the hospital. Oxycodone
as a controlled-release tablet can provide good pain
control for up to 12 hours. This may be supplemented by
oxycodone immediate-release concentrated solution or
capsule for breakthrough pain.
Nonsteroidal anti-inflammatory drugs
Nonsteroidal anti-inflammatory drugs are used widely
to treat pain and inflammation. They do not carry the
same side effects of the opiates; therefore, although
they are less potent than the narcotics, they can act as
opiate-sparing agents.
The development of more potent and parenteral
nonsteroidal anti-inflammatory analgesics such as
ketorolac has led to an increase in their use. These
drugs are particularly useful in managing the pain
associated with minimally invasive surgery.
However, associated side effects include peptic ulcer
disease, gastrointestinal hemorrhage, renal
dysfunction, altered liver function, and platelet
dysfunction. These side effects limit the use of these
agents in many patients during the perioperative period.
Nonsteroidal anti-inflammatory drugs act by inhibiting
the enzyme cyclooxygenase (COX), which is responsible for
the synthesis of prostaglandins. Prostaglandins are
responsible for pain, fever, and vasodilatation in
response to trauma. The major drawback of these
medications is that they also block the beneficial
effects of the prostaglandins: the decrease in the tissue
inflammatory response to surgical trauma and the
concomitant reduction in peripheral nociception and pain
perception.
COX-2 inhibitors
There are 2 isoforms of COX: COX-1 and COX-2. COX-1 is
found in various tissues. The prostaglandin it produces
protects gastric mucosa, limits acid secretion, enhances
renal perfusion, and preserves platelet function. COX-2,
instead, is induced by pain and inflammation. Therefore,
COX-2 inhibitors can alleviate pain and inflammation
without the deleterious side effects of the regular
nonsteroidal drugs, which block both enzymes (13).
These COX-2 inhibitors are now available for oral use.
A parenteral preparation is under clinical trial for
postoperative pain control and has been shown to be
comparable to ketorolac in analgesia potency but without
its deleterious side effects (14). This new group of
analgesics may be safer and may eventually play a more
extensive role in the management of acute postoperative
pain.
Regional techniques
Epidural and spinal analgesia have been shown to
improve surgical outcomes by decreasing intraoperative
blood loss, postoperative catabolism, and the incidence
of thromboembolic events, and by improving vascular graft
blood flow and postoperative pulmonary function (15).
Epidural and spinal opioids provide better analgesia than
systemic opioids, but the side effects are still present
and therefore monitoring protocols are necessary. The
neuroaxial narcotics may cause insidious delayed
respiratory depression, and pruritus may occur in a
significant number of patients.
Local anesthetics may cause hypotension and muscle
weakness that may slow down mobilization. To reduce the
narcotic side effects, low concentrations of local
anesthetic, such as ropivacaine 0.2%, may be added to the
infusion. This concentration is weak enough to avoid
motor weakness.
One of the most dangerous complications in the
placement of an epidural catheter is the development of a
spinal hematoma. The risk of this complication is
increased in patients receiving anticoagulant therapy
(16). In patients receiving thromboprophylaxis with
low-molecular-weight heparin, epidural catheter placement
or removal should be delayed until 12 hours from the last
administration. Anticoagulant therapy and surgery should
also be delayed 12 hours in patients who have suffered a
bloody tap during placement of the catheter
(16).
Close neurological monitoring is required for patients
who have had an epidural catheter inserted, so that an
epidural hematoma will be detected early in its
development. If a hematoma is suspected, magnetic
resonance imaging should be performed immediately.
Evacuation of the epidural clot within 8 hours of symptom
onset is crucial for recovery of neurological function
(16).
The increasing use of perioperative anticoagulant
therapy and the increase in nursing surveillance required
for neuroaxial analgesic techniques have promoted the
resurrection of the paravertebral block. Although first
described in 1905 by Hugo Sellheim of Leipzig
(1871-1936), the paravertebral block has only recently
become popular (17). The paravertebral space is a
wedge-shaped area between the heads and necks of the
ribs. The contents of each space include the spinal
nerve, its dorsal ramus, the rami communicantes, and the
sympathetic chain. Therefore, an accompaniment of the
somatic block is a localized unilateral sympathetic
block. This block is particularly effective for
unilateral surgical procedures such as thoracotomy,
breast surgery, cholecystectomy, and renal surgery. There
is a low incidence of adverse effects, and patients
require no additional nursing care. This block can be
performed safely in patients on anticoagulants. Because
of its low side effect profile, the paravertebral block
contributes to accelerated postoperative mobilization.
Nonpharmacologic techniques
Opioid and nonopioid analgesics all come with
potential side effects. Therefore, alternative therapies
have been explored with varying success. Electrical
stimulation of peripheral nerves may influence pain
inhibitory pathways, inhibit substance-P release, and
perhaps cause the release of endogenous opiate substances
(18). The efficacy of these modalities in reducing the
requirement for conventional pain medications is still
controversial.
PEDIATRIC PAIN MANAGEMENT
Children experience pain differently than adults do.
Their emotional development, previous experiences, and
ability to communicate and understand are all
imponderable variables. A needle stick to an adult may be
just an isolated unpleasant event, whereas to a child it
may be the epitome of the evil of their disease (19).
Pain assessment in children is more challenging than
in adults. Children are not malingerers; they are very
open about expressing their feelings. Nevertheless, it
may not be easy for the pain therapist to differentiate
between pain and distress.
As the emotional component of pain is very strong in
children, psychological support is very important.
Minimal separation from parents, holding, nurturing,
and distraction are all important modalities.
Nonopioid analgesics such as acetaminophen or
nonsteroidal anti-inflammatory agents are useful for
mild pain control and as an opiate-sparing measure. Oral,
rectal, or intravenous routes are the preferred methods
of administration of analgesics--children do not care for
intramuscular injections. Intravenous fentanyl, morphine,
and meperidine are the most popular opiates.
Patient-controlled analgesia has been used successfully
even with very young children. Regional analgesia
performed while the patient is under general anesthesia
can provide excellent early postoperative pain relief.
PREEMPTIVE ANALGESIA
Analgesia administered before the painful stimulus
occurs may prevent or substantially reduce subsequent
pain or analgesic requirements. This hypothesis has
prompted numerous clinical studies, but few robust
studies have clearly demonstrated its efficacy. A recent
study examined the administration of epidural fentanyl or
bupivacaine prior to surgical incision in patients
undergoing radical prostatectomy. The study group
experienced less postoperative pain and at follow-up 9
weeks later were more active sooner compared with the
control group (20). This study supports the concept that
protecting the nervous system preemptively reaps rewards
later.
THE FUTURE
As a result of a better understanding of the
mechanisms and physiology of acute pain and nociceptors,
the goal of a stress-free anesthetic with minimal
postoperative discomfort is attainable. No single therapy
can achieve this goal. A multimodal approach using
different drugs and techniques can reap the highest
benefit and reduce the side effects. Some newer agents
that may offer better therapeutic benefits are
dexmedetomidine and remifentanil.
Dexmedetomidine
Dexmedetomidine is a highly selective, centrally
active alpha-2-adrenergic agonist that provides both
sedation and analgesia without significant ventilatory
depression. Phase III studies in postoperative patients
have shown that a continuous infusion of 0.2 to 0.7
?g/kg/hr easily maintains a patient at a Ramsay Sedation
Score of 3 with a significant morphine-sparing effect
and, most importantly, with no evidence of respiratory
depression (21). The properties of this novel drug
indicate it could be used intravenously even into the
recovery period, with more safety than many presently
available sedatives and analgesics. It may lend itself as
a sole anesthetic agent for conscious sedation.
Remifentanil
Remifentanil is a very potent ?-opioid receptor
agonist that is rapidly metabolized by circulating
nonspecific esterases and rapidly cleared. It can provide
very controllable analgesia depending on infusion rate.
However, there are 2 potential dangers: it is a very
potent narcotic and will cause respiratory depression,
and its rapid metabolism means that its analgesic effect
will dissipate rapidly once the infusion is terminated.
In the intensive care setting, remifentanil can be
carefully titrated to provide total analgesia to
postoperative patients. However, in the extubated
patient, the window between good analgesia and
significant respiratory depression is small. We have
demonstrated that it is as effective as a thoracic
epidural analgesic in the postoperative management of
lung transplant patients (22).
CONCLUSION
Advances in pharmacology, techniques, and education
are making major inroads into the management of
postoperative pain. Nursing education, patient care, and
physician responsiveness will be key to the success of
any pain management improvement initiative.
- Sharrock NE, Cazan MG, Hargett
MJ, Williams-Russo P, Wilson PD Jr. Changes
in mortality after total hip and knee
arthroplasty over a ten-year period. Anesth
Analg 1995;80:242-248.
- Katz J, Jackson M, Kavanagh
BP, Sandler AN. Acute pain after thoracic
surgery predicts long-term post-thoracotomy
pain. Clin J Pain 1996;12:50-55.
- Pollock RE, Lotzova E,
Stanford SD. Mechanism of surgical stress
impairment of human perioperative natural
killer cell cytotoxicity. Arch Surg
1991;126:338-342.
- Lennard TW, Shenton BK,
Borzotta A, Donnelly PK, White M, Gerrie LM,
Proud G, Taylor RM. The influence of surgical
operations on components of the human immune
system. Br J Surg 1985;72:771-776.
- Kehlet H. Modification of
response to surgery and anesthesia by neural
blockade: clinical implications. In Cousins
MT, Bridebaugh PO, eds. Neural Blockade in
Clinical Anesthesia and Management of Pain,
3rd ed. Philadelphia: Lippincott, 1998.
- Ashburn MA, Love G, Pace NL.
Respiratory-related critical events with
intravenous patient-controlled analgesia. Clin
J Pain 1994;10:52-56.
- Etches RC. Respiratory
depression associated with patient-controlled
analgesia: a review of eight cases. Can J
Anaesth 1994;41:125-132.
- Hutton P, Clutton-Brock T. The
benefits and pitfalls of pulse oximetry. BMJ
1993;307:457-458.
- Rudolph F, Hein HAT, Marcel
RJ, Swygert TH, Lynch K, Ramsay KJ, Ramsay
MAE. End-tidal carbon dioxide does not
correlate with arterial carbon dioxide in
early recovery from general anesthesia. Anesth
Analg 1998;86:S227.
- Ramsay MA, Savege TM, Simpson
BR, Goodwin R. Controlled sedation with
alphaxalone-alphadolone. Br Med J
1974;2:656-659.
- Maze M. Sedation in the
intensive care environment. In Vincent JL,
ed. Yearbook of Intensive Care and
Emergency Medicine. Berlin: Springer,
2000:405-413.
- White PF. Use of
patient-controlled analgesia for management
of acute pain. JAMA 1988;259:243-247.
- Kurumbail RG, Stevens AM,
Gierse JK, McDonald JJ, Stegeman RA, Pak JY,
Gildehaus D, Miyashiro JM, Penning TD,
Seibert K, Isakson PC, Stallings WC.
Structural basis for selective inhibition of
cyclooxygenase-2 by anti-inflammatory agents.
Nature 1996;384:644-648.
- Mehlisch D, Kuss M, Bauman A,
Baum D, Hubbard R. Onset and duration of
analgesia of single IM doses of parecoxib and
toradol in post-operative dental pain. In
Proceedings of the 9th World Congress
on Pain, 1999, Vienna. Seattle: IASP
Press, 2000.
- Yeager MP, Glass DD, Neff RK,
Brinck-Johnsen T. Epidural anesthesia and
analgesia in high-risk surgical patients. Anesthesiology
1987;66:729-736.
- Vandermeulen EP, Van Aken H,
Vermylen J. Anticoagulants and
spinal-epidural anesthesia. Anesth Analg
1994;79:1165-1177.
- Richardson J, L?nnquist PA.
Thoracic paravertebral block. Br J Anaesth
1998;81:230-238.
- Cheng RS, Pomeranz BH.
Electroacupuncture analgesia is mediated by
stereospecific opiate receptors and is
reversed by antagonists of type I receptors. Life
Sci 1980;26:631-638.
- Lewis N. The needle is like an
animal: how children view injections. Child
Today 1978;7:18-21.
- Gottschalk A, Smith DS, Jobes
DR, Kennedy SK, Lally SE, Noble VE, Grugan
KF, Seifert HA, Cheung A, Malkowicz SB,
Gutsche BB, Wein AJ. Preemptive epidural
analgesia and recovery from radical
prostatectomy: a randomized controlled trial.
JAMA 1998;279:1076-1082.
- Hall JE, Uhrich TD, Barney JA,
Arain SR, Ebert TJ. Sedative, amnestic, and
analgesic properties of small-dose
dexmedetomidine infusions. Anesth Analg
2000;90:699-705.
- Ramsay KJ, Ramsay MAE, Joshi
G, Hein HAT, Bishara L, Cancemi E.
Remifentanil versus thoracic epidural
analgesia in lung transplantation. Anesth
Analg 1998;86:S93.
|