Moderate or severe pain are important sources of complications as well as morbidity and mortality in the postoperative period after surgical procedures. Patient‐controlled analgesia (PCA) is an effective strategy for postoperative analgesia, since it may provide suitable analgesic dose just after system activation, with reduced periods of pain and an increase in patients’ satisfaction. Although intravenous and epidural routes are the typical approaches used for PCA, regional patient‐controlled analgesia has been shown to be an effective alternative providing a higher standard of analgesia with lower incidence of adverse effects. New devices and routes of PCA administration (transdermal, sublingual, inhalation, and oral routes) have shown to be promising alternatives in clinical studies. Nowadays, there is still no consensus regarding which is the best route or drug used since clinical efficacy/safety depends on the complex comprehension of the drugs pharmacokinetic profile through different routes of administration. Additionally, pharmacoeconomic studies are needed to evaluate the cost‐effectiveness of these approaches.
- patient‐controlled analgesia
- acute pain
- analgesic medication
The International Association for Study of Pain defines pain as an unpleasant experience, with or without tissue damage, which can be related to individual memories, life expectations and emotions . The painful experience involves interpretation of biological aspects of pain and its interaction with social and cultural characteristics .
In surgical procedures, moderate to severe pain can be observed in up to 40% of cases , representing an important source of complications as well as morbidity and mortality in the postoperative period . Postoperative pain can limit mobility and respiratory function, increasing the incidence of atelectasis, pneumonia and thromboembolic events [5, 6].
Moreover, the lack of adequate pain control in acute situations can lead to chronic pain, with deleterious effects for the patient and health‐related quality of life . Despite these findings, between 50% to 75% of those submitted to major surgery do not receive enough analgesic medication, increasing the risk of complications and length of stay and costs for the health system .
Morphine was isolated by a German pharmacist Friedrich Wilhem Sertürner in 1806 and, after that, opioids have become widely used in clinical practice for pain control. Later in 1844, parenteral administration of morphine has started after the introduction of glass syringe .
In 1963, Roe demonstrated that administration of small doses of intravenous morphine allowed a better pain control compared to intramuscular injections . Sechzer, in 1968, was the first to evaluate the quality of analgesia after administration of small doses of opioids
Since then, several drugs and routes of administration have been used in PCA, with differences in analgesic efficacy, tolerability profile, adverse effects, and procedure‐related complications as well as patient satisfaction .
2. PCA: principles and pharmacological aspects
The principle of intravenous PCA was first described by Austin et al. in 1980, after he administrated small increasing doses of meperidine and measured the plasma levels, demonstrating the dose‐related analgesic effect in patients .
Despite being associated with the idea of pump with intravenous opioids, there are several routes of administration, drugs, and equipment that can be used in this mode of analgesia. It is essential that, for the PCA recommendation, individual pain pattern and intensity be considered.
The patients must be previously and duly enlightened on the technical procedure and their consent should be obtained. As desirable characteristics of PCA, we can highlight the adequate pain relief according to individual requirements, the tolerance and safety profile of drugs administered, the high level of patients’ satisfaction and minimal complications related to technological aspects .
In order to understand the effectiveness of PCA, we need to understand the concept of “minimal effective analgesic concentration (MEAC).” The MEAC is defined as the smallest concentration at which the pain is relieved .
Considering the existence of individuals’ variability, the MEAC cannot be determined from the plasma levels of opioids. It is known that the plasma concentration is a function related to the dose, dosage intervals, gender and age of the patient. It can be calculated based on pharmacokinetic concepts such as volume of distribution and distribution and elimination rates. However, in clinical situations, the plasma levels are not able to predict the pattern of analgesic response . Tamsen et al. showed that the MEAC has a direct correlation with preoperative concentrations of endogenous opioids and substance P in the cerebral spinal fluid. Obviously, the achievement of these measurements is restricted in clinical practice .
For the PCA effectiveness, the MEAC should be achieved by titration, which means that the drug is administered as a
Regardless of the route or administered drug, the two main types of PCA are: the demand dosing (the fixed dose which is self‐administered intermittently) and continuous infusion associated with demand dosing (the constant‐rate fixed background infusion is supplemented by patient demand dosing), whereas the principles of a fixed infusion administration as well as principles of variation of the infusion rates managed by a period of time are considered .
Some basic principles and technical parameters are common to several modalities. They are initial loading dose, demand dose, interval lockout, and background infusion rate.
The initial dose usually is not administered by the patient, since the goal of first administration is to promote adequate pain control or prevent the early pain manifestation. This approach allows the establishment of the demand dose, also called PCA dose or
The lockout interval is a set period in which the equipment does not perform a new infusion of demand. During the interval lockout, if the patient triggers the button, he/she will not receive the medication. Normally, the equipment has a sound signal connected to the drive, regardless of the infusion, so that the patient does not know whether his/her requests were effective. The lockout interval has the primary function of security by preventing the administration of an overdose of analgesic drugs. The background infusion rate is a given infusion rate in a continuous manner, independent of the patient's wish (also called continuous infusion). The 1‐h and/or 4‐h limits, depending on the equipment configuration, it has the function to limit the total cumulative dose in the period of 1 or 4 h in order to reduce the adverse effects and ensure the patient safety [11, 18].
Considering the advances in the development of drug delivery systems, the use of infusion pumps for patient‐controlled analgesia (PCA) and analgesia epidural catheter with opioids are considered the most powerful strategies to control of postoperative pain. However, there are doubts about the advantages and limitations of these different forms of PCA.
The basal opioid administration doses may be administered concurrently with the administration of opioids by PCA techniques. However, the basal administration increases the risk of respiratory depression without providing necessarily an additional analgesia pattern .
PCA different modalities can minimize the occurrence of gaps in analgesic administration, supplying analgesic dosage immediately after the system activation, providing more uniform analgesia and eliminating painful waiting periods between the patient's request and drug administration.
3. PCA modalities
Electronic PCA pumps have several models in the market, including small portable devices nowadays. Since the first commercially available PCA pump (“Cardiff Palliator”), PCA devices have evolved enormously in technological sophistication, ease of use, flexibility and portability.
3.1. Intravenous PCA (IV‐PCA)
Currently, IV‐PCA is one of the most used techniques for acute pain control. Its use is suitable for virtually any patient undergoing surgery that are cursed with postoperative pain of moderate or severe intensity . Many studies have demonstrated the efficacy, safety, and patient satisfaction with PCA intravenously. A meta‐analysis involving 115 randomized clinical trials demonstrated that this technique provides greater efficacy when compared to intramuscular administration of analgesics . Another study showed that, among patients who received IV‐PCA, 36% experienced moderate to severe pain in the first 24 h after surgery when compared to 67% of important painful experience among patients who received intramuscular opioids . Moreover, it was verified that the IV‐PCA is associated with a higher rate of patient satisfaction .
Despite the possibility that IV‐PCA may be combined to a basal opioids infusion, it was shown that the incidence of respiratory depression with IV‐PCA was much smaller (0.19% versus 0.29%) when compared to the combination of this technique with systemic infusion of opioids (1.09–3% versus 8%) .
IV‐PCA is associated with potential complications inherent in the technique, which are operator‐dependent. Errors may occur in the drug administration, usually by programming failures on infusion pump  and they may result in inadequate pain control, heavy sedation, respiratory depression, and, eventually, death of the patient . Currently, many infusion pumps feature smart devices that are equipped with an integrated software library on dosing regimens of different drugs, thus avoiding underdosing or overdosing. In these models, the smart bombs are programmed to stop operation or to alert clinicians when doses exceed the limits .
However, serious errors can still occur even with smart bombs. According to the Food and Drug Administration (FDA), 56,000 adverse events with these smart bombs during the period 2005–2009 have been reported .
Several complications may be observed from the IV‐PCA, such as clogging or dislodgement of catheters, intervals between the administrations of opiates for maintenance of analgesic effect . Still, this technique implies in risk for adverse effects related to opioids .
Furthermore, IV‐PCA limits mobility and it reduces the comfort of the patient who is connected to the infusion pump, which can be minimized by using more modern compact equipment. Zafar et al.  reported that about 21% of patients who received IV‐PCA complained of reduced mobility. It is worth noting, finally, the economic aspect, as a limitation of the technique, as well as the need of equipment (infusion pump) and the discarding of remaining solutions after the PCA use, causing unnecessary costs for health services [12, 30].
The major drugs used in this system are the opioid analgesics, such as morphine, hydromorphone, fentanyl, sufentanil and tramadol . Meperidine is no longer considered a valid option for PCA as its toxic metabolite may be accumulated, especially in patients with abnormal kidney function . Therefore, meperidine has not been recommended for acute pain .
Morphine is the most common opioid used for IV-PCA and it is considered the gold standard for this procedure. Although many studies have demonstrated its clinical safety, adverse effects such as nausea, vomiting, itching, urinary retention, sedation and respiratory depression may occur. Its active metabolite morphine‐6‐glucuronide (M6G) have analgesic action but presents risk of adverse effects. As the M6G has renal elimination, the use of morphine should be done with caution in patients with impaired renal function and the elderly [34, 35]. The low therapeutic index of morphine in IV‐PCA was shown in preclinical models, indicating that morphine cannot be the best option for all patients for pain relief in the postoperative period .
The usual morphine dose and the recommended parameters are: demand dose: 1–2 mg; lockout period: 6–10 min; continuous basal infusion dose: 0–2 mg/h .
Hydromorphone has been used in patients with impaired renal function or with a history of allergy to morphine. It is mainly metabolized by the liver and it is, approximately, five times more potent than morphine. Clinical effects of hydromorphone are dose‐dependent and its adverse event profile is morphine‐like [11, 36]. A systematic review of adverse events associated with the postoperatory use of six different opioids (buprenorphine, fentanyl, hydromorphone, meperidine, morphine, and sufentanil) showed that after meperidine (proscribed, 67.9%), the opioid with the highest incidence of central nervous system side effects was hydromorphone (42.7%). Furthermore, at higher doses, hydromorphone can cause excitation .
Due to the similarity between morphine and hydromorphone, errors have been reported in programming the IV‐PCA pump. Considering that these agents have significant differences in their clinical potency, inadvertent hydromorphone administration can result in serious complications .
Doses and recommended parameters are: demand dose: 0.2–0.4 mg; lockout period: 6–10 min; continuous basal infusion dose: 0–0.4 mg/h .
Fentanyl is 80–100 times more potent than morphine and it may cause less respiratory depression when compared with morphine. It has no active metabolites, and it has a wider therapeutic index than morphine in preclinical models .
In a retrospective cohort study of 8955 patients who received one of the three opioids for postoperative pain (morphine, fentanyl or meperidine), the incidence of respiratory depression was 0.6% in the group of patients who received fentanyl, compared to 2.8% among patients who received morphine . Although apparently it may be associated with smaller risk of respiratory depression when compared to morphine, fentanyl can be associated with more device programming errors, since this drug is dosed in micrograms [40, 41].
Because of its high lipid solubility, fentanyl has a pharmacokinetic profile characterized by a rapid onset and short action. Therefore, some patients may need doses too frequently or require a basal infusion rate, which greatly increases the risk of respiratory depression. Due to its high volume of distribution, prolonged administration may result in a significant increase in drug half‐life, with consequent raise in the incidence of adverse effects . Given these pharmacokinetic characteristics, there are complaint reports of patients after fentanyl administration in IV‐PCA .
Doses and recommended parameters: demand dose: 20–50 µg; lockout: 5–10 min; Basal continuous: 0–60 µg/h .
Sufentanil is a fentanyl analog, being about 5–10 times more potent than Fentanyl itself. It represents the opioid with greater therapeutic index (25,000) used for postoperative pain in preclinical studies . The high therapeutic index is clinically relevant for evoking a decreased risk of incidence of respiratory depression compared to morphine, fentanyl, and alfentanil . In a randomized clinical trial with 30 volunteers, it was noted that sufentanil provided more effective analgesia and less respiratory depression when compared with fentanyl .
Sufentanil is highly lipophilic (twice more lipophilic than fentanyl) and it provides rapid onset of action and shorter effect duration when administered intravenously to PCA, justifying its rare use in this route. However, unlike fentanyl, its half‐life of elimination does not increase with infusion time and it shows paradoxical increase in their concentration during the elimination phase . A randomized clinical trial that compared plasma levels of sufentanil and fentanyl in 41 patients undergoing coronary artery bypass surgery, demonstrated the occurrence of peak plasma concentration (increase of 29–49%) from 4 to 15 h after administration
The doses and the usual parameters are: demand dose: 4–6 µg; lockout: 5–10 min; continuous baseline: 0–8 µg/h .
Tramadol acts on opioid receptors with higher affinity for κ receptors than δ and μ receptors. It has an active metabolite, mono‐O‐desmethyl (M1), which has analgesic effect. In addition to the opioid agonist activity, tramadol analgesia is also promoted by inhibiting the central norepinephrine and serotonin reuptake. Tramadol potency compared to morphine is approximately 0.1. Several studies have shown that tramadol is a safe and an effective option for PCA, but with a higher incidence of nausea and vomiting [46, 47]. The recommended doses are: demand dose: 10–20 mg; lockout: 6–10 min; continuous baseline: 0–20 mg/h .
Oxycodone is an opioid μ receptor agonist indicated for the treatment of moderate to severe pain. Despite being most frequently used orally, in recent years, its intravenous use has increased. Its potency is about 1/75 of fentanyl, and in some studies has shown great potency up to 1/60 [48, 49].
A randomized clinical trial with 82 patients compared IV‐PCA with oxycodone and fentanyl. In this study, oxycodone demonstrated potency of 1/55 of fentanyl for the same levels of analgesia, being equally safe and the same incidence of adverse effects such as nausea, vomiting and sedation . It is a drug with good efficacy and a promising role in the practice of PCA. Its use must be made on demand associated with basal infusion. The recommended doses are: demand bolus: 1 mg; lockout: 15 min; background infusion rate: 1 mg/h .
3.1.7. Other drugs
Other opioids have been less used in IV‐PCA. The alfentanil, probably due to their pharmacokinetic characteristics, did not show good results and a demand dose was not established to present a satisfactory analgesia . The remifentanil, because of their ultrashort half‐life, does not have a favorable profile for PCA with some indication for analgesia for a short period such as during labor .
Other drugs have been used by some authors that are normally associated with morphine. Ketamine, which is an agonist of the NMDA receptor, and naloxone, which is an antagonist of opioid receptors, have shown conflicting results regarding the safety or quality of analgesia, and more studies are needed so that they can get their recommended use .
3.2. Epidural PCA
Epidural patient‐controlled analgesia (EPCA) is the second most significant method used and studied within the PCA approach. Its use is mainly for control of acute postoperative pain, commonly in patients undergoing orthopedic, abdominal and thoracic surgery . EPCA allows the use of opioids, local anesthetics, or a combination of both. Opioids epidural administered provide greater analgesic potency when compared to equivalent doses of opioid administered intravenously .
Although both opioids and local anesthetics represent feasible options, local anesthetics are the most appropriate strategies for patients sensitive to the opioids adverse effects, even though it is associated with a higher incidence of hypotension, motor block and urinary retention compared with the use of opioids . Similarly to the PCA intravenous technique, EPCA allows patients to administer the medication in accordance with analgesic requirements. There is large evidence indicating that the EPCA represents a safe and effective method [46, 54]. A meta‐analysis concluded that, regardless of the drug chosen, epidural provides a better analgesia pattern when compared to intravenous PCA technique .
In a population‐based study of 2276 surgical patients, Kim et al.  discloses that ropivacaine with fentanyl was able to provide good quality analgesia for up to 48 h after the several surgical procedures, with limited side effects .
Unlike IV‐PCA, the use of continuous infusion, coupled with the demand dose, have shown excellent results with minimal complications. Small doses of local anesthetics of long action combined with low doses of opioids (i.e., fentanyl or sufentanil) with continuous infusion rate associated with increments
Despite many advantages, EPCA also has limitations, especially considering the complexity of the procedure and technical staff training. In addition, there are reports of catheter migration which may lead to failure in the procedure in 17% of cases. It has been suggested that this technique has great effectiveness but it should be used with caution considering individual factors, in order to ensure patient safety .
3.3. Patient‐controlled regional analgesia
There are several techniques that use catheters for the purpose of providing postoperative analgesia with little or no opioid use. In this model of patient‐controlled regional analgesia, local anesthetics (ropivacaine, bupivacaine or levobupivacaine) are normally administered through a catheter located in perineural site, intraarticular region or surgical incision site. Eventually, a combination of local anesthetics and opioids can be administered by the infusion pump .
Several studies have addressed the effectiveness of this method for postoperative analgesia . Vintar et al.  noted that about 80% of patients who received bupivacaine and ropivacaine at the incision site were satisfied with the outcome of the procedure and said they would use this treatment again.
Studies emphasizing the intraarticular administration of opioids and/or local anesthetics are rare. Vintar et al. , in a controlled clinical trial, describes that the group which received the combination of ropivacaine/morphine/ketorolac required less use of rescue analgesics in relation to other groups.
It is estimated that, during orthopedic surgery, drug administration by intraarticular can provide 12–15 h of analgesia . In this context, the most efficient strategy would be the infusion of local anesthetics via epidural. Additionally, the brachial plexus, lumbar plexus and femoral nerve and sciatic nerve are examples of sites for drugs infusion. In a clinical trial, the PCRA ropivacaine 0.2% in the brachial plexus region was effective in shoulder orthopedic surgery regarding pain intensity, opioids’ use as rescue medication, and less sleep disorders .
In a multicenter study involving orthopedic surgeries, the perineural ropivacaine administration by continuous infusion or PCRA was compared to intravenous morphine. Patients receiving morphine showed higher levels of postoperative pain and required higher consumption of analgesic as rescue medication, significantly increasing the side effects such as nausea, vomiting, dizziness and sleep disturbances .
3.4. Other modalities of patient‐controlled analgesia
The iontophoretic fentanyl system (IONSYS; Ortho‐McNeil, Raritan, NJ, USA) is a preprogrammed noninvasive method of PCA, which does not require venous access for drug administration. By adhesively secured to the outside of the arm or chest of the patient, fentanyl is transferred iontophoretically through intact skin. The system allows the transdermal administration of the drug for 10 min and a 10 min lockout interval between administrations .
However, the fentanyl dose administered over time is not constant. Whereas the target dose for the desired effect of fentanyl is 40 µg, it is estimated that the average dose is 16 µg after the initial application. Therefore, it would take a long period of time until the optimal dose is reached. Many patients do not receive adequate analgesia for up to 10 h after the start of the application .
Although clinical studies have suggested that the use of transdermal fentanyl could show similar efficacy to morphine in PCA intravenously in relation to the overall control of pain , there was a need for additional analgesia in 40% of patients involved in the first 3 h of treatment. Moreover, there were local side effects such as skin redness in about 60% of cases. This system was not marketed in the U.S. and it was withdrawn from the European market by the manufacturer due to a manufacturing error in some units .
A new sublingual administration system using sufentanil (AcelRx Pharmaceuticals, Redwood City, CA, USA) is designed as a microtablet coupled to a preprogrammed portable device with locking features and radio frequency identification to enable the characterization of a single user. Although intravenous sufentanil present a short half‐life context‐dependent due to its rapid redistribution, pharmacokinetic studies in healthy subjects showed that after sublingual administration, sufentanil has adequate profile for the postoperative analgesia .
Sufentanil NanoTabs® shows high bioavailability and plasma half‐life and it is safer than the administration of the drug intravenously to avoid the need for frequent administrations of the lipophilic opioids commonly used for this procedure. Several clinical trials have demonstrated its efficacy in pain relief in different types of orthopedic and abdominal surgery, having been described few side effects to this method .
Several products using the inhalation of PCA to opioid administration are described in the literature. Thipphawong et al.  tested a morphine inhalation system (System AERx Pain Management; Aradigma Corporation, Hayward, CA, USA), which had desirable characteristics of a drug for PCA (possibility of multiple dosing with lock time between them and observed similar efficacy to morphine IV‐PCA).
Similarly, fentanyl (AeroLEF, YM Biosciences, Mississauga, ON, Canada) also had proven to control postoperative pain following orthopedic surgery. However, further studies are needed to confirm the effectiveness of opioids in this route, especially clinical trials phase III and IV.
The intranasal opioid administration is possible, since the nasal mucosa has an extensive vascularization, providing rapid drug absorption and distribution .
The presentation of intranasal morphine (Rylomine®, Javelin Pharmaceuticals Inc., Cambridge, MA, USA) was effective for the control of postoperative pain in orthopedic surgery . However, the single dose after a nasal administration does not have the desirable safety features of PCA models, such as the possibility of multiple dosages and lock scheduled time between applications. Other opioids have been tested for intranasal administration but similar to morphine, these devices also did not have the desirable features of a PCA device. In this context, Toussaint et al.  noted that intranasal fentanyl administration showed similar efficacy compared to IV‐PCA fentanyl. Intranasal sufentanil was also successfully used both in adults and pediatric patients .
However, this route may have local adverse effects: nasal irritation, nasal congestion, upper respiratory tract infections, sinusitis, rhinitis, pharyngitis, or epistaxis, which may be a limitation of its clinical use .
Oral PCA device (Avancen, Mount Pleasant, SC, USA) is a drug unit coupled to a bracelet programmed to keep out of the drug for a predetermined time interval. After this lockout period, a green light indicates the possibility of new management. The equipment is compact and allows the patient to make the registration of pain on a scale of 0–10, providing feedback to the health team.
In a study of this device with hydromorphone administration, oxycodone and morphine, it was reported better control of pain in 95% of patients who used these devices when compared to the control group. Furthermore, it highlighted the ease of programming of this device by the health team .
Although this oral device for PCA is a good alternative, there are few studies regarding its safety. It is noteworthy of some shortcomings: lack of clinical efficacy in cases of moderate to severe pain, management failure in patients in whom oral administration is not available and uncertain absorption in the immediate postoperative period.
Patient‐controlled analgesia (PCA) is a great option for acute pain control. Several advantages of this technique can be highlighted, such as higher analgesic standard with patient's satisfaction, and also minor side effects. However, there is still no consensus regarding which is the best route or drug used since clinical efficacy/safety depends on the complex comprehension of the pharmacokinetic drugs profile through different routes of administration. Additionally, pharmacoeconomic studies are needed to evaluate the cost‐effectiveness of these approaches.
Loeser JD, Treede RD. The Kyoto protocol of IASP Basic Pain Terminology. Pain 2008;137:473–77.
Kopf A, Patel NB, editors. Guide for Pain Management in Low‐Resources Settings. 1st ed. United States: International Association for the Study of Pain – IASP Press; 2010.
Power I. Recent advances in postoperative pain therapy. Br J Anaesth 2005;95(1):43–51.
Mueller XM, Tinguely F, Tevaearai HT, et al. Pain location, distribution and intensity after cardiac surgery. Chest 2000;118(2):391–6.
Johnson D, Kelm C, Thomson D, et al. The effect of physical therapy on respiratory complications following cardiac valve surgery. Chest 1996;109(3):638–44.
Ulke ZS, Senturk M. Non‐analgesic effects of thoracic epidural anesthesia. Agri 2007;19(2):6–12.
Boddy AP, Metha S, Rhodes M. The effect of intraperitoneal local anesthesia in laparoscopic cholecystectomy: a systematic review and meta‐analysis. Anesth Analg 2006;103:682–88.
Giacomazzi CM, Lagni VB, Monteiro MB. A dor pós‐operatória como contribuinte do prejuízo na função pulmonar em pacientes submetidos a cirurgia cardíaca. Braz J Cardiovasc Surg 2006;21(4):386–92.
Roe BB. Are postoperative narcotics necessary?. Arch Surg 1963;87:912–15.
Evans JM, Rosen M, MacCarth J, Hogg MI. Apparatus for patient‐controlled administration of intravenous narcotics during labour. Lancet 1976;I:17–8.
Grass JA. Patient‐controlled analgesia. Anesth Analg 2005;101:S44–61.
Viscusi ER. Patient‐controlled drug delivery for acute postoperative pain management: a review of current and emerging technologies. Reg Anesth Pain Med 2008;33(2):146–58.
Austin KL, Stapleton JV, Mather LE. Relationship between blood meperidine concentrations and analgesic response: a preliminary report. Anesthesiology 1980;53:460–6.
Dahlstrom B, Tamsen A, Paalzow L, Hartvig P. Patient‐controlled analgesic therapy, Part IV: pharmacokinetics and analgesic plasma concentrations of morphine. Clin Pharmacokinet 1982;7:266–79.
Tamsen A, Sakaruda T, Wahlstrom A, et al. Postoperative demand for analgesics in relation to individual levels of endorphines and substance P in cerebral spinal fluid. Pain 1982;13:171–82.
Ferrante FM, Covino BG. Patient‐controlled analgesia: a historical perspective. In: Ferrante FM, Ostheimer GW, Covino BG, editors. Patient‐controlled Analgesia. Boston: Blackwell Scientific Publications; 1990, pp. 3–9.
Ferrante FM. Patient‐controlled analgesia: a conceptual framework for analgesic administration. In: Ferrante FM, Vadeboncouer TR, editors. Postoperative Pain Management. 1st ed. New York: Churchill Livingston; 1993, pp. 255–277.
Mann C, Ouro‐Bangna F, Eledjam JJ. Patient‐controlled analgesia. Curr Drug Targets 2005;6:815–9.
Hagle ME, Lehr VT, Brubakken K, Shippee A. Respiratory depression in adult patients with intravenous patient‐controlled analgesia. Ortho Nurs 2004;23:18–27.
Ballantyne JC, Carr DB, Chalmers TC, et al. Postoperative patient‐controlled analgesia: meta‐analyses of initial randomized controlled trials. J Clin Anesth 1993;5:182–93.
Dolin SJ, Cashman JN, Bland JM. Effectiveness of acute postoperative pain management: I. Evidence from published data. Br J Anaesth 2002;89:409–23.
Lebovits AH, Zenetos P, O’Neill DK, Cox D, Dubois MY, Jansen LA, Turndorf H. Satisfaction with epidural and intravenous patient‐controlled analgesia. Pain Med. 2001;2:280–6.
Schug SA, Torrie JJ. Safety assessment of postoperative pain management by an acute pain service. Pain 1993;55:387–91.
Vicente KJ, Kada‐Bekhaled K, Hillel G, Cassano A, Orser BA. Programming errors contribute to death from patient‐controlled analgesia: case report and estimate of probability. Can J Anaesth 2003;50:328–32.
Hankin CS, Schein J, Clark JA, Panchal S. Adverse events involving intravenous patient‐controlled analgesia. Am J Health Syst Pharm 2007;64:1492–9.
Rothschild JM, Keohane CA, Cook EF, et al. A controlled trial of smart infusion pumps to improve medication safety in critically ill patients. Crit Care Med 2005;33:533–40.
Center for Devices and Radiological Health, US Food and Drug Administration. Infusion Pump Improvement Initiative. April 2010.
Panchal SJ, Damaraju CV, Nelson WW, et al. System‐related events and analgesic gaps during postoperative pain management with the fentanyl iontophoretic transdermal system and morphine intravenous patient‐controlled analgesia. Anesth Analg 2007;105:1437–41.
Miaskowski C. Patient‐controlled modalities for acute postoperative pain management. J Perianesth Nurs 2005;20(4):255–67.
Zafar SU, Hamid M, Hoda MQ. Patient controlled intravenous analgesia (PCIA) in postoperative surgical patients: an audit. J Pak Med Assoc 2004;54(7):353–6.
Hutchison RW, Chon EH, Tucker WF, et al. A comparison of fentanyl, morphine and hydromorphone patient‐controlled intravenous delivery for acute postoperative analgesia: a multicenter study of opioid‐induced adverse reactions. Hosp Pharm 2006;41:659–63.
Simopoulos TT, Smith HS, Peeters‐Asdourian C, et al. Use of meperidine in patient‐controlled analgesia and the development of a normeperidine toxic reaction. Arch Surg 2002;137:84–8.
American Society of Pain. Principles of Analgesic Use in the Treatment of Acute Pain and Cancer Pain. 6th Edition: Glenvile, IL: American Society of Pain; 2008.
Momeni M, Crucitti M, Kock MD. Patient‐controlled analgesia in the management of postoperative pain. Drugs 2006;66:2321–37.
Ratka A, Wittwer E, Baker L, et al. Pharmacokinetics of morphine, morphine‐3‐glucoronide, and morphine‐6‐glucoronide in health older men and women. Am J Pain Manage 2004;14:45–55.
Hong D, Flood P, Diaz G. The side‐effects of morphine and hydromorphone patient‐controlled analgesia. Anesth Analg 2008;107:1384–9.
Wheeler M, Oderda GM, Ashburn MA, et al. Adverse events associated with postoperative opioid analgesia: a systematic review. J Pain 2002;3:159–80.
Palmer PP, Royal MA, Miller RD. Novel delivery systems for postoperative analgesia. Best Pract Res Clin Anaesthesiol 2014;18:81–90.
Palmer PP, Miller RD. Current and developing methods of patient‐controlled analgesia. Anesthesiol Clin 2010;28(4):587–99.
Cepeda MS, Farrat JT, Baugarten M, et al. Side‐effects of opioids during short term administration: effect of age, gender and race. Clin Pharmacol Ther 2003;74:102–12.
Scott LJ. Fentanyl iontophoretic transdermal system: a review in acute postoperatory pain. Clin Drug Investig 2016;36:321–30.
Egan TD, Lemmens HJ, Fiset P, et al. The pharmacokinetics of the new short‐acting opioid remifentanil (GI87084B) in healthy adult male volunteers. Anesthesiology 1993;79:881–92.
Prakash S, Fatima T, Pawar M. Patient‐controlled analgesia with fentanyl for burn dressing changes. Anesth Analg 2004;99:552–5.
Bailey PL, Streisand JB, East KA, et al. Differences in magnitude and duration of opioid‐induced depression and analgesia with fentanyl and sufentanil. Anesth Analg 1990;70:8–15.
Stoeckel H, Schuttler J, Magnussen H, et al. Plasma fentanyl concentrations and the occurrence of respiratory depression in volunteers. Br J Anaesth 1982;54:1087–95.
Silvasti M, Pitaknen M. Patient‐controlled epidural analgesia versus continuous epidural analgesia after total knee arthroplasty. Acta Anaesthesiol Scand 2001;45:471–6.
Erolcay H, Yuceyar L. Intravenous patient‐controlled analgesia after thoracotomy: a comparison of morphine with tramadol. Eur J Anaesthesiol 2003;20:141–6.
Sjovall S, Kokki M, Kokki H. Laparoscopy surgery: a narrative review of pharmacotherapy in pain management. Drugs 2015;75(16):1867–89.
Park JH, Lee C, Shin Y, An JH, Ban JS, Lee JH. Comparison of oxycodone and fentanyl for postoperative patient‐controlled analgesia after laparoscopic gynecological surgery. Korean J Anesthesiol 2015;68:153–8.
Jung KW, Kang HW, Park CH, Choi BH, et al. Comparison of the analgesic effect of patient‐controlled oxycodone and fentanyl for pain management in patients undergoing colorectal surgery. Clin Exp Pharmacol Physiol 2016;43(8):745–52.
Owen H, Brose WG, Plummer JL, Mather LE. Variables of patient‐controlled analgesia. Test of an infusion‐demand system using alfentanil. Anesthesia 1990;452–5.
Thurlow JA, Laxton CH, Dick A, et al. Remifentanil by patient‐controlled analgesia compared with intramuscular meperidine for pain relief in labor. Br J Anaesth 2002;88:374–8.
Sinatra RS, Torres J, Bustos AM. Pain management after major orthopaedic surgery: current strategies and new concepts. J Am Acad Orthop Surg 2002;10:117–29.
Saito M, Okutomi T, Kanai Y, Mochizuki J, Tani A, Aamano K, Hoka S. Patient‐controlled epidural analgesia during labor using ropivacaine and fentanyl provides better maternal satisfaction with less local anesthetic requirement. J Anesth 2005;19:208–12.
Wu CL, Cohen SR, Richman JM, et al. Efficacy of postoperative patient‐controlled and continuous infusion epidural analgesia versus intravenous patient‐controlled analgesia with opioids: a meta‐analysis. Anesthesiology 2005;103:1079–88.
Kim SH, Yoon KB, Yoon DM, et al. Patient‐controlled epidural analgesia with ropivacaine and fentanyl: experience with 2,276 surgical patients. Korean J Pain 2005;26(1):39–45.
Leon‐Casasola OA, Parker BM, Lema MJ, Groth RI, Orsini‐Fuentes J. Epidural analgesia versus intravenous patient‐controlled analgesia. Differences in the postoperative course of cancer patients. Reg Anesth 1994;19(5):307–15.
Liu SS, Allen HW, Olsson GL. Patient‐controlled epidural analgesia with bupivacaine and fentanyl on hospital wards: prospective experience with 1,030 surgical patients. Anesthesiology 1998;88(3):688–95.
Fredman B, Shapiro A, Zohar E, et al. The analgesic efficacy of patient‐controlled ropivacaine instillation after Cesarean delivery. Anesth Analg 2000;91:1436–40.
Vintar N, Pozlep G, Rawal N, Godec M, Rakovec S. Incisional self‐administration of bupivacaine or propivacaine provides effective analgesia after inguinal hernia repair. Can J Anaesth 2002;49:481–86.
Ilfeld BM, Morey TE, Wright TW, Chidgey LK, Enneking FK. Continuous interscalene brachial plexus block for postoperative pain control at home: a randomized, double‐blinded, placebo‐controlled study. Anesth Analg 2003;96:1089–95.
Capdevila X, Dadure C, Bringuier S, Bernard N, Biboulet P, Gaertner E, Macaire P. Effect of patient‐controlled perineural analgesia on rehabilitation and pain after ambulatory orthopedic surgery: a multicenter randomized trial. Anesthesiology 2006;105:566–73.
Thipphawong JB, Babul N, Morishige RJ, Findlay HK, Reber KR, Millward GJ, Otulana BA. Analgesic efficacy of inhaled morphine in patients after bunionectomy surgery. Anesthesiology 2003;99(3):693–700.
Stoker DG, Reber KR, Waltzman LS, et al. Analgesic efficacy and safety of morphine‐chitosan nasal solution in patients with moderate to severe pain following orthopedic surgery. Pain Med 2008;9:3–12.
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;47(4):299–302.
Dale O, Hjortkjaer R, Kharasch ED. Nasal administration of opioids for pain management in adults. Acta Anaesthesiol Scand 2002;46:759–70.