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PCA
vs continuous infusion
L.
Bertini Department
of Anaesthesia and Intensive Care CTO
Hospital Rome
Italy
Despite a growing trend in acute
pain management, many deficiencies still account for the high incidence
of moderate to severe postoperative pain to date. Patients nowadays
continue to receive inadequate doses of analgesics, but additionally
the identification and treatment of those patients with pain still remains
a significant health care problem. Advanced techniques are available
including epidural or intrathecal administration of local anaesthetics
and opioids, various opioid administration techniques such as patient-controlled
analgesia and infusions, or via sublingual, oral-transmucosal, nasal,
intra-articular and rectal routes. Non-opioid analgesics such as non-steroidal
anti-inflammatory drugs and newer non-opioid drugs such as alpha2-adrenergic
agonists, calcium channel antagonists and various combinations of the
above are possible. However, the solution to the problem of inadequate
pain relief lies not so much in the development of new drugs and new
techniques, but in the effective strategy of delivering these to patients.
The administration of opioids
and local anaesthetics with patient controlled anaesthesia (PCA) is
becoming ever more common in the treatment of acute postoperative pain
[i]
. This technique is used in several different ways of administration:
aside from the widely known intravenous way, PCA is also performed in
epidural analgesia
[ii]
, in peripheral plexus continuous blockade
[iii]
[iv]
[v]
and also by nasal
[vi]
[vii]
or oral administration. The popularity of this technique
is also accompanied by an increased concern over its safety, especially
regarding the incidence of respiratory depression and its possible lethal
consequences. Such scepticism is sometimes a result of a widespread
opiophobia very common in Italy, where morphine usage is
among the lowest in Europe. The
theoretical advantages of patient-controlled administration are self-evident:
if patients are enabled to press a button and receive their opioid dose
only when they feel pain, the total amount of administered drug will
be most likely reduced with respect to a continuous infusion. Such procedure
allows patients to adjust their doses to suit their variable needs,
as the demand for analgesics is only rarely constant throughout the
day. For example, its quite evident how active or passive movement,
or even cough may exacerbate perceived pain. There is also evidence
that postoperative pain might function on a circadian rhythm characterised
by a significant increase at night
[viii]
. PCA technique has an intrinsic
safety control, in that patients who start to develop respiratory depression
are correspondingly sedated, thus usually unable to request any more
(potentially dangerous) doses. Decreased consumption of drugs and a
higher patient satisfaction rate have been demonstrated with this procedure
[ix]
. Clinical trials performed on over 10,000 patients have
shown that the incidence of significant respiratory depression (such
as to require medical intervention) is around 0.2%viii
. This value is lower than that found with patients treated with
intra-muscular opioids, which is 0.9%
[x]
[xi]
. The incidence of respiratory depression was also considerably
higher in studies performed in the 1980s on patients who were given
continuous intravenous opioid infusionx
. The usage of a basic continuous infusion in association with
PCA seems to increase the risk of the dangerous complication to 1.65%
of the cases
[xii]
[xiii]
. In a study performed on 4,000 patients, only 9 of them
had any respiratory complications, and in those cases the side-effects
were always associated with pharmacological interactions, continuous
opioid infusion or nurse/physician-controlled analgesia
[xiv]
. Also in childhood, the addition of a background continuous
opioid infusion seems to increase the risk of adverse effects with no
actual improvement of the pain score
[xv]
. Comparative studies show that continuous infusion does
not reduce bolus demand, but instead increases the total amount of administered
drug
[xvi]
[xvii]
[xviii]
. Continuous infusion may also reduce the safety of PCA,
as it is administered independently of the patients sedation level
(whereas a sedated patient cannot request additional boluses!). In the
light of current knowledge, a continuous background opioid infusion
in conjunction with PCA does not seem to have any advantages over PCA-only
postoperative analgesia
[xix]
[xx]
. As suggested in the American Society of Anesthesiologists
guidelines, continuous infusion together with PCA is only indicated
in patients who are already on an opioid therapy, or in addicted patients
treated with methadone
[xxi]
. In such patients, continuous infusion dose should be around
50% of the estimated daily demand, the rest being administered through
PCA
[xxii]
. Because of all these considerations,
PCA is now universally accepted as the safest technique for intravenous
opioid administration in the treatment of acute postoperative pain. The recommended bolus dose in
adults under 70, derived from extensive experience conducted throughout
most Western countries, is 1 mg morphine (or equivalent dosage of other
drugs), with no background infusion and on a 5 minutes lockout.
In patients of age 70 and over, these doses should be reduced by 30%. PCA has recently been employed
in epidural analgesia (PCEA), and although only limited data is available
to date, several authors have confirmed its efficacy. In PCEA studies,
a background infusion is often associated with the on-demand administration,
in order to better adjust drug administration to the patients
needs. It is thought that an intermittent opioid and/or local anaesthetic
infusion would not allow the patient to rest comfortably during the
first postoperative night. In one of the first studies on PCEA from
Chrubasik
[xxiii]
, the administration of morphine in epidural PCA proved effective,
and seemed to allow a reduction of drug usage and side-effects, but
no control group had been included in that study.
In another work from Ferrante, PCEA was compared against a continuous
epidural infusion (CEI), obtaining similar levels of analgesia, but
also a reduction in bupivacaine and fentanyl hourly consumption in patients
treated with PCEA
[xxiv]
. Owen studied the incidence of hypoxaemia (<90%) in abdominal
surgery patients given epidural analgesia with continuous fentanyl infusion,
PCEA and CEI + PCEA
[xxv]
. There was a significant reduction in hypoxaemic episodes
and administered fentanyl doses in patients with PCEA. Other authors
have found similar decrease in drug dosage, but also worse pain control
during movement compared to CEI
[xxvi]
. More information is available regarding PCEA in obstetrics.
Also in such patients, drug usage seems to be reduced by up to 40% in
comparison with CEI
[xxvii]
. There are also indications of a decreased incidence of
instrumental and cesarean deliveries, although more evidence is needed
to confirm this data
[xxviii]
. Other authors have noticed similar patients satisfaction
scores and decreased drug usage in PCEA patients. PCEA is well accepted now in
the treatment of postoperative pain. Besides the higher costs, some
substantial differences are noticed in comparison with continuous infusion.
Because pain scores alone, both at rest and during movement are not
the sole parameter to evaluate an analgesic regimen, benefits may be
assessed also in terms of dose sparing effects, reduced incidence of
side-effects, thromboembolic prophylaxis, sympatholysis, earlier gastro-intestinal
recovery and, consequently, discharge from the hospital. More studies
are needed to understand the actual effects of PCEA. At present time
PCEA with a basal rate is most probably the best compromise when using
opioid/local anaesthetic combinations since the effect of deleting the
concurrent infusion upon the above mentioned beneficial effects has
not been established yet. Although until now such a device
is not available from a pharmacokinetic and dynamic point of view, it
would be most inviting to give local anaesthetic at a constant rate
while simultaneously administering additional opioids by PCEA
[xxix]
. Doing so, both the patient and the anaesthetist may participate
in optimal tuning of pain relief. PCA is used also in peripheral
nerve blocks, particularly for open shoulder surgery and knee surgery.
Continuous infusion of 0.125% bupivacaine or 0.2% ropivacaine at a rate
of 8-10 ml/h is often considered the gold standard
[xxx]
. However, this involves large volumes of local anaesthetic
with potential risk of toxicity. Singelyn demonstrated that a lower
basal infusion rate (5 ml/h) of bupivacaine associated with PCA boluses
(2.5 ml, lockout 30 min) provided comparable pain relief, but significantly
reduced the consumption of local anaesthetic
[xxxi]
. This technique reduced the incidence of side effects (Horners
syndrome, clinical phrenic nerve palsy), and allowed reinforcement of
the block shortly before physiotherapy. PCA boluses alone were unable
to maintain adequate analgesia during continuous interscalene block.
Sensory block decreased considerably below the analgesic threshold during
sleep (pain appeared systematically during the first postoperative night)
and PCA bolus size and/or lockout were inappropriate to restore it.
Also continuous axillary plexus block, after major hand surgery gives
an easy, safe and efficient analgesic technique. It provides lower postoperative
pain scores and less side effects than i.v. PCA. Recently Iskandar
[xxxii]
demonstrated the efficacy of PCA technique alone (boluses
of 0.25% bupivacaine: 0.1 mg/Kg lockout 1 hour) after severe
hand trauma surgery. When compared with a continuous infusion this technique
provided comparable analgesia, but significantly reduced (by 69%) local
anaesthetic consumption. Moreover in the PCA group, 94% of patients
were satisfied or very satisfied with the technique instead of 43% in
the other group. Similar results were obtained when a continuous infusion
of a combination of bupivacaine, sufentanil and clonidine was compared
with PCA boluses of the same mixture for postoperative analgesia by
3 in1 block after both knee and hip surgery. Again there was no difference
between the groups as regards pain scores, rescue medication and satisfaction
scores. However, total bupivacaine consumption was significantly lower
in the PCA groups. In conclusion, PCA alone or
with a background infusion results in effective analgesia in all ways
of administration with a high degree of patient satisfaction. With PCA,
patients are in control of an important part of the therapy they receive,
and this power in an otherwise extraneous environment might be the key
to a successful treatment of postoperative pain.
[ii]
Wiebalck A, Brodner G, Van Aken H. The effects
of adding sufentanil to bupivacaine for postoperative patient-controlled
epidural analgesia. Anesth
Analg. 1997 Jul;85(1):124-9.
[iii]
Riedl V, Buchfelder A, Kellermann W, Schwender
D. Patient-controlled analgesia versus continuous interscalenar plexus
blockade: effectivity of the postoperative pain management after open
shoulder surgery [abstract]. Br J Anaesth 1997;78:A417
[iv]
Borgeat A, Schäppi B, Biasca N, Gerber C. Patient-controlled analgesia
after major shoulder surgery. Anesthesiology 1997;87:13437.
[v]
Borgeat A, Tewes E, Biasca N, Gerber C. Patient-controlled interscalene
analgesia with ropivacaine after major shoulder surgery: PCIA vs PCA.
Br J Anaesth 1998;81:6035.
[vi]
Hallett A,O'Higgins F, Francis V, Cook TM. Patient-controlled
intranasal diamorphine for postoperative pain: an acceptability study.
Anaesthesia 2000 Jun;55(6):532-9
[vii]
Toussaint S, Maidl J, Schwagmeier R, Striebel
HW. Patient-controlled intranasal analgesia: effective alternative
to intravenous PCA for postoperative pain relief. Can J Anaesth 2000
Apr;47(4):299-302
[viii]
Miller RR, Greenblatt DJ. Drug
effects in hospitalized patients. John Wiley and Sons, New York 1976,
pp 151-152
[ix]
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therapy. Anaesthesist 1997 Oct; 46 Suppl 2:S124-31
[x]
Sidebotham D, Dijkhuizen MR, Schug SA. The safety and utilization of
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[xi]
Norman J. Theoretical and practical requirements for PCA systems. In
Harmer M, Rosen M, Vickers MD, eds: Patients controlled analegsia,
Oxford, 1984, Blackwell Scientific
[xii]
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[xiii]
Owen H, Szekely SM, Plumer JL, Cushnie JM, Mather LE. Variables of patient-controlled
analgesia: 2. Concurrent infusion. Anaesthesia 1989; 44: 11-13
[xiv]
Looi Lyons LC, Chung FF, Chan VW,
McQuestion M. Respiratory depression: an adverse outcome during patient
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[xv]
Weldon BC,- Connor M,- White PF.- Pediatric PCA:
the role of concurrent opioid infusions and nurse-controlled analgesia.
Clin J Pain 1993 Mar; 9(1):26-33
[xvi]
Russell AW, Owen H, Ilsey AH, Kluger MT,
Plummer JL. Background
infusion with patient-controlled analgesia: effect on postoperative
oxyhaemoglobin saturation and pain control. Anaesth Intensive Care
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[xvii]
Doyle E, Robinson D, Morton NS. Comparison of patient-controlled analgesia with and without
a background infusion after lower abdominal surgery in children. Br
J Anaesth 1993; 71: 670-3
[xviii]
Parker RK, Holtmann
B, White PF. Patient-controlled analgesia: failure of opioid infusion
to improve pain management after surgery. JAMA 1991;226:1947-52
[xix]
Parker RK, Holtmann B, White PF. Patient-controlled
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[xx]
Ready LB, Ashburn M, Calan RA, Carr BD, Connis
RT, Dixon CL, Hubbard L, Rice LJ. Practice guidelines for Acute Pain
Management in the Perioperative Setting a report of the American
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[xxi]
Ferrante FM. Opioids: In Postoperative Pain Management
(eds Ferrante and VadeBoncouer TR) Churchill Livingston, New York
1993 pp 134
[xxii]
Chrubasik J, Wiemers K. Continuous-plus-on-demand
epidural infusion of morphine for postoperative pain relief by means
of a small, externally worn infusion device. Anesthesiology 1985;62:263-267
[xxiii]
Chrubasik J, Wiemers K. Continuous-plus-on-demand
epidural infusion of morphine for postoperative pain relief by means
of a small, externally worn infusion device. Anesthesiology 1985;62:263-267
[xxiv]
Ferrante FM, Lu L, Jamison SB, Datta S. Patient-controlled epidural analgesia:
demand dosing. Anesth
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[xxv]
Owen H, Kluger MT, Ilsley AH, Baldwin AM,
Fronsko RR, Plummer JL.The effect of fentanyl administered epidurally
by patient-controlled analgesia, continuous infusion, or a combined
technique of oxyhaemoglobin saturation after abdominal surgery. Anaesthesia
1993 Jan; 48(1):20-5
[xxvi]
Boudreault D, Brasseur L, Samii K, Lemoing
JP. Comparison
of continuous epidural bupivacaine infusion plus either continuous
epidural infusion or patient-controlled epidural injection of fentanyl
for postoperative analgesia. Anesth
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[xxvii]
Tan S, Reid J, Thorburn J.Extradural analgesia
in labour: complications of three techniques of administration. Br
J Anaesth 1994 Nov; 73(5):619-23
[xxviii]
Collis RE, Plaat FS, Morgan BM. Comparison of
midwife top-ups, continuous infusion and patient-controlled epidural
analgesia for maintaining mobility after a low-dose combined spinal-epidural.
Br J Anaesth 1999 Feb; 82(2):233-6
[xxix]
Boudrealt D, Brasseur L, Samii K, Lemoing J.
Comparison of continuous epidural bupivacaine infusion plus either
continuous epidural infusion or patient controlled injection of fentanyl
for postoperative analgesia. Anesth Analg 1991: 73:132
[xxx]
Pere P. The effect of continuous interscalene
brachial plexus block with 0.125% bupivacaine plus fentanyl on diaphragmatic
motility and ventilatory function. Reg
Anesth 1993;18:9397
[xxxi]
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Seguy, MD and J. M. Gouverneur, MD Interscalene Brachial
Plexus Analgesia After Open Shoulder Surgery: Continuous Versus Patient-Controlled
Infusion Anesth Analg 1999 Nov; 89(5):1216-20
[xxxii]
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