Skip to main content
Anesthesiology and Pain Medicine logoLink to Anesthesiology and Pain Medicine
. 2016 Mar 2;6(2):e36461. doi: 10.5812/aapm.36461

Evaluating Persistent Postoperative Pain in One Tertiary Hospital: Incidence, Quality of Life, Associated Factors, and Treatment

Luis Guimaraes-Pereira 1,*, Ines Valdoleiros 1, Pedro Reis 1, Fernando Abelha 1,2
PMCID: PMC4886451  PMID: 27252908

Abstract

Background

Persistent postoperative pain (PPP) is defined as persistent pain after surgery of greater than three months’ duration.

Objectives

Identify the incidence of PPP in our hospital and its associated factors; evaluate quality of life (QoL) and treatment of patients.

Patients and Methods

We conducted an observational prospective study in adults proposed to various types of surgery using the brief pain inventory short form preoperatively (T0), one day after surgery, and three months later (T3). If the patient had pain at T3 and other causes of pain were excluded, they were considered to have PPP, and the McGill Pain Questionnaire Short Form was applied. QoL was measured with the EuroQol 5-dimension questionnaire (EQ-5D).

Results

One hundred seventy-five patients completed the study. The incidence of PPP was 28%, and the affected patients presented lower QoL. The majority referred to a moderate to severe level of interference in their general activity. Cholecystectomies were less associated with PPP, and total knee/hip replacements were more associated with it. Preoperative pain, preoperative benzodiazepines or antidepressants, and more severe acute postoperative pain were associated with the development of PPP. Half of the patients with PPP were under treatment, and they refer a mean symptomatic relief of 69%.

Conclusions

This study, apart from attempting to better characterize the problem of PPP, emphasizes the lack of its treatment.

Keywords: Chronic Pain, Postoperative Pain, Quality of Life

1. Background

Persistent postoperative pain (PPP) is considered a silent epidemic that is in urgent need of better understanding of its pathophysiology (1). The consequences of PPP can be variable, from mild to severe loss of quality of life (QoL). The international association for the study of pain (IASP) defines it as persistent pain after surgery of greater than three months’ duration (1). Before making a diagnosis of PPP, it is critical that other common causes of pain from surgery be ruled out.

The first publication that identified surgery as a major risk factor for chronic pain appeared in 1998 (2). An important increase in interest in this subject has occurred since that publication.

The problem is not limited to major surgery, as even minor procedures such as herniotomy can have important consequences with regard to development of PPP. Some consider it the most common and serious long-term problem after repair of an inguinal hernia (3).

The consequences of PPP are significant, not only in terms of suffering and reduced QoL for the individual patient, but also with regard to the subsequent costs to the health care and social support systems of our societies (4).

The incidence of PPP varies according to definition and surgical procedure, ranging from 5% to 50% (1). Recently, in a cross-sectional survey performed in Norway, PPP was reported by 40.4% of the patients, with moderate to severe PPP reported by 18.3% (5). In a Portuguese cross-sectional epidemiological study, 6% of patients with chronic pain attributed its etiology to surgery (6).

In 2013, the Portuguese directorate-general of health published a strategic plan for prevention and control of pain (7). One of its guiding principles is the duty of pain control, and it states that all health professionals should adopt strategies for prevention and control of pain in their patients. It is also mentioned that particular attention should be given to the prevention and management of pain caused by diagnostic or therapeutic acts.

The majority of publications about PPP address issues such as definition, incidence, risk factors, preventive strategies, and the evolution of pain. However, the treatment of established PPP is less studied. Previous studies have confirmed the severe multidimensional impact of chronic pain, as the QoL of patients with chronic non-malignant pain is among the lowest observed for any medical condition (8, 9). Due to its importance, we decided to study this problem in our hospital.

2. Objectives

To identify the incidence of PPP in our hospital; to identify factors associated with the development of PPP; and to evaluate QoL and current treatment of patients with PPP.

3. Patients and Methods

We conducted an observational prospective study approved by our institutional ethics committee. Informed consent was obtained from each patient included in the study. The study protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki as reflected in the approval by our institutional ethics committee. We included adults proposed to surgery in June 2013. As we would not be able to study all surgeries scheduled in our hospital, we decided to include thoracotomies, hysterectomies, mastectomies, inguinal hernia repairs, thyroidectomies, laparoscopic cholecystectomies, amputations, and total knee or hip replacements (TKHR). The choice of these surgical procedures was made after a reunion of anesthesiologists to take into account the procedure’s relevance and logistics. Patients with American society of anesthesiologists (ASA) physical status 4 were excluded. We registered age, gender, ASA physical status, medical history, and current medications for all patients.

The type of anesthesia was administered according to the type of surgery. Thoracotomies and hysterectomies were performed under combined anesthesia (general anesthesia plus epidural anesthesia). Mastectomies, inguinal hernia repairs, thyroidectomies, and laparoscopic cholecystectomies were performed under general anesthesia. Amputations and TKHR were performed under spinal anesthesia, and an epidural catheter was also placed to administer postoperative analgesia. The anesthetic protocol in general anesthesia was standardized in all patients: midazolam, fentanyl, and propofol were used for induction of anesthesia, and patients were paralyzed with rocuronium or cisatracurium. Anesthesia was maintained with sevoflurane or desflurane and either fentanyl or remifentanil, as preferred by the attending anesthesiologist. Epidural analgesia with local anesthetic plus opioid and intravenous analgesia according to the world health organization’s analgesic ladder were used in thoracotomies, hysterectomies, amputations, and TKHR. Intravenous analgesia according to the world health organization’s analgesic ladder was used in the other surgeries. Our acute pain unit works 24 hours per day, every day of the week, and provides acute pain care according to recommended standards.

Sample size was calculated for an incidence of 35%, a confidence interval of 90%, and a margin of error of 5%, and the result was 175 patients.

We applied the validated Portuguese version of the brief pain inventory short form (BPI-SF) (10) preoperatively (T0), one day after surgery (T1), and three months later (T3). The BPI-SF evaluates pain severity on an 11-point numerical rating scale (from 0 or “no pain” to 10 or “worst pain imaginable”), pain interference in daily activities (general activity, mood, walking, work, interpersonal relations, sleep, and enjoyment of life), intake of pain analgesics, perception of analgesic relief, and pain location (11). BPI-SF is a valid instrument to measure pain in patients with and without cancer (11, 12).

At T3, the first question asked was “Do you still have any pain that you could relate to the surgical procedure?” This is an adaptation of the BPI-SF first question on pain prospection, and it was performed in other similar studies (13). If the patient answered “yes” and other causes of pain were excluded, he or she was considered as having PPP, and we applied the Portuguese version of the McGill pain questionnaire short form (MPQ-SF). The MPQ-SF is a useful tool in situations in which the standard questionnaire takes too long to administer, yet qualitative information is desired (14). Patients with PPP were also asked about their current pain treatment: intake of pain medications, analgesic prescribers, and perception of analgesic relief.

QoL was measured with the Portuguese version of the EuroQol 5-Dimension questionnaire (EQ-5D) at T0 and T3. EQ-5D is a standardized instrument to measure health outcome, and contains five dimension questions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression (15). The Portuguese version of the EQ-5D has good accessibility, reliability, and validity in measuring health (16).

All questionnaires were administered after previous authorizations from their authors. For analysis purposes, we converted the numeric rating used in BPI-SF into categorical variables: “0” to none, “1 - 3” to mild, “4 - 6” to moderate, and “7 - 10” to severe. Non-parametric and parametric tests were performed for comparison between numerical variables according to their distribution, and a chi-square test for categorical variables.

4. Results

We recruited 190 patients, and 175 patients completed the study. We were unable to contact 15 patients at T3. Table 1 presents the main characteristics of our sample. The incidence of PPP was 28% (49 patients) according to IASP definition (1) and the incidence of moderate to severe PPP was 12.6%.

Table 1. Characteristics of the Sample (N = 175)a.

Variable Values
Age, y (M, [P 25 - P 75 ]) 63 [48.0 - 70.5]
Gender
Male 35.8
Female 64.2
ASA physical status
I 13.7
II 63.2
III 23.1
Surgical Specialty
Thoracic Surgery 7.7
General Surgery 59.2
Vascular Surgery 10.9
Gynecology 5.9
Orthopedics 11.2
Plastic Surgery 5.1

Abbreviations: M, Median; P25, 25th percentile; P75, 75th percentile.

aValues are expressed as percentage except foe age.

Table 2 presents the PPP severity and interference assessed with BPI-SF. We did not detect any differences in pain severity and interference among the specific surgeries. According to the MPQ-SF, patients with PPP presented a 6.5 median sensory pain rating index, a 0.0 median affective pain rating index, and a 6.5 median total pain rating index. We did not find differences in pain rating indexes between surgical groups.

Table 2. Persistent Postoperative Pain Severity and Interference Assessed With Brief Pain Inventory Short Form (n = 49).

Parameters Level of Pain/Interference
No Pain/No Interference Mild Moderate Severe
Pain Severity
Average Pain - 27 (55.1) 19 (38.8) 3 (6.1)
Worst Pain - 10 (20.4) 17 (34.7) 22 (44.9)
Least Pain 30 (61.2) 16 (32.7) 2 (4.1) 1 (2.0)
Pain at interview 14 (28.6) 24 (49.0) 7 (14.3) 4 (8.1)
Interference
General Activity 10 (20.4) 12 (24.5) 11 (22.4) 16 (32.7)
Mood 16 (32.7) 13 (26.5) 6 (12.2) 14 (28.6)
Work 12 (24.5) 11 (22.4) 10 (20.4) 16 (32.7)
Relations with others 24 (49.0) 14 (28.6) 5 (10.2) 6 (12.2)
Sleep 20 (40.8) 14 (28.6) 7 (14.3) 8 (16.3)
Enjoyment of life 22 (44.9) 11 (22.4) 10 (20.4) 6 (12.3)

Regarding acute postoperative pain, the worst pain considered severe in the first 24 hours was associated with higher incidence of PPP (38.8% vs 19.8%, P = 0.01). The average pain considered moderate to severe in the first 24 hours was also associated with development of PPP (40.8% vs. 23.0%, P = 0.019).

Relative to surgical groups (Table 3), cholecystectomies were less associated with the development of PPP (8.3% vs. 31.1%, P = 0.021), and TKHR were more associated with it (50.0% vs. 25.5%, P = 0.028).

Table 3. Persistent Postoperative Pain Among the Surgical Groups (n = 49).

N in the 1st Group PPP in the 1st Groupa PPP in Othersa P Valueb
Amputation vs. Others 14 30.8 27.8 0.817
Laparoscopic cholecystectomy vs. Others 24 8.3 31.1 0.021
Thoracotomy vs. Others 14 15.4 29.0 0.292
Inguinal hernia repair vs. Others 29 27.6 28.1 0.957
Hysterectomy vs. Others 13 25.0 28.2 0.81
TKHR vs. Others 19 50.0 25.5 0.028
Mastectomy vs. Others 38 25.5 36.8 0.17
Thyroidectomy vs. Others 24 29.1 20.8 0.4

Abbreviations: N, number of patients; PPP, persistent postoperative pain; TKHR, Total knee or hip replacement.

aValues are expressed as percentage.

bChi-square Test.

We were unable to detect differences for gender, age, body mass index, diabetes, and statin medication prior to surgery (Table 4). The percentage of patients with PPP was higher in those with any preoperative pain in the related area (51.4% vs. 21.5%, P < 0.001), even when we exclude patients with presence of acute postoperative pain (55.5% vs. 10.1, P = 0.002). Patients with a history of prior surgery in the related area had a higher incidence of PPP (50.0% vs. 24.5%, P = 0.01). However, when we exclude patients with preoperative pain, there is no difference in the incidence of PPP (24.0% vs. 14.3%, P = 0.228). Patients with prior surgery in the related area had more preoperative pain when compared to those without it (26.3% vs. 7.1%, P = 0.008).

Table 4. Persistent Postoperative Pain and Associated Factors (n = 49)a.

PPP Without PPP P Value
Preoperative Pain 38.3 13.8 < 0.001b
Preoperative Pain excluding patients with pain at 24 hours 50.0 9.1 0.002b
Postoperative Pain at 24 hours 75.0 53.7 0.021b
Postoperative Pain at 24 hours excluding patients with preoperative pain 79.2 50.0 0.011b
Gender 0.125b
Male 26.5 38.9
Female 73.5 61.1
Body Mass Index, (Median, P 25 - P 75 ), kg/m 2 26 (24 - 28) 26 (23 - 30) 0.495c
Age, Median, P 25 - P 75 63 (53 - 71) 61 (46 - 69) 0.077c
Diabetes 14.3 21.4 0.284b
UM with Benzodiazepines 36.7 19.2 0.015b
UM with Statins 24.5 32.3 0.479b
UM with Antidepressives 38.8 9.8 < 0.001b
Prior surgery in the related area 24.5 9.5 0.01b

Abbreviations: PPP, persistent postoperative pain; UM, usual medication.

aValues are expressed as percentage except for body mass index and age.

bChi-square Test.

cMann-Whitney U Test.

Average postoperative pain considered severe in the first 24 hours was associated with higher incidence of PPP, when compared to those with lower scores (71.4% vs. 26.2%, P = 0.009). Conversely, average postoperative pain considered mild in the first 24 hours was associated with lower incidence of PPP, when compared to higher scores (24.3% vs. 52.2%, P = 0.006). Incidence of PPP was higher in patients with the presence of any acute postoperative pain (37.0% vs. 18.5%, P = 0.021), even when we exclude patients with preoperative pain (32.2% vs. 11.1%, P = 0.011).

Regarding QoL using EQ-5D, none of the EQ-5D dimensions presented a normal distribution (the Kolmogorov-Smirnov test was performed). Initially, EQ-5D dimension distributions were not different for patients with or without PPP, except for pain dimension (M: P = 0.24; SC: P = 0.197; UA: P = 0.149; pain: P < 0.001; AD: P = 0.341; Mann-Whitney test performed). However, three months later, patients with PPP presented lower results in all EQ-5D dimension distributions (mobility: P = 0.01; self-care: P < 0.001; usual activities: P < 0.001; pain: p < 0.001; anxiety/depression: P < 0.001; Mann-Whitney test performed).

Anxiety and depression problems, measured initially with EQ-5D as previously noted, were not associated with the development of PPP (29.6% vs. 24.1%, P = 0.341). However, PPP was positively associated with preoperative current treatment with benzodiazepines (42.9% vs. 23.5%, P = 0.015) or antidepressants (61.3% vs. 21.3%, P < 0.001). The associations are maintained after excluding patients with preoperative pain (benzodiazepines: 37.5% vs. 16.7%, P = 0.013; antidepressants: 50.0% vs. 16.2%, P < 0.001). Later on, PPP patients presented more problems related to anxiety and depression at T3 (54.1% vs. 20.6%, P < 0.001). Even when we exclude the patients who previously were taking antidepressants or benzodiazepines, this association is maintained (35.0% vs. 14.1%, P = 0.027). Anxiety and depression problems were associated with higher scores for BPI-SF and pain rating indexes in patients with PPP (Table 5).

Table 5. Relation Between Anxiety/Depression and Values Obtained in Pain Scales (n = 49).

Pain Severity in BPI Pain Interference in BPI Sensory Pain Rating Index Affective Pain Rating Index Total Pain Rating Index
Median (P25 - P75) Median (P25 - P75) Median (P25 - P75) Median (P25 - P75) Median (P25 - P75)
Anxiety/Depression
absent to mild 2.8 (1.8 - 4.0) 1.14 (0.3 - 3.6) 6.0 (3.0 - 8.0) 0.0 (0.0 - 1.0) 6.0 (3.0 - 9.0)
moderate to extreme 3.6 (2.6 - 4.8) 4.9 (3.0 - 6.4) 9.0 (6.0 - 13.0) 2.0 (0.0 - 3.0) 10.0 (6.0 - 14.0)
P Value a < 0.001 0.047 0.001 0.041 0.002

Abbreviations: BPI, brief pain inventory; P25, 25th percentile; P75, 75th percentile.

aMann-Whitney U test.

In our sample, 53.1% of the patients with PPP were under treatment (96.2% with medication and 3.8% with physiotherapy). The rest of the patients (46.9%) had no treatment. Regarding their classification of average pain, treatment was performed in 37.0% of the patients with mild pain, 68.4% of the patients with moderate pain, and in all (100.0%) patients with severe pain. According to their classification of worst pain, treatment was performed in 40.0% of the patients with mild pain, 47.1% of the patients with moderate pain, and in 63.3% of the patients with severe pain. General practitioners are responsible for treatment in 61.5% of the patients, and surgeons for 34.6%. Only one patient was being treated in a Chronic Pain Unit. Acetaminophen was the only analgesic prescribed for 65.4% of the patients under treatment. Patients under treatment refer a mean symptomatic relief of 69%.

5. Discussion

The incidence of PPP in our study is in accordance with the literature (1, 17). However, this comparison has some limitations, as many studies have different methodologies. An important percentage of our patients have PPP, which deserves special attention and intervention from health authorities and professionals, as PPP represents a major humanitarian and socioeconomic burden (18).

The incidence of PPP was different among the selected surgical groups, which is also in accordance with the current literature. Previous studies revealed that chronic abdominal pain after cholecystectomy is common, ranging between 3% to 56%, whether open or laparoscopic (19). In a procedure-specific study, 18% of the patients submitted to laparoscopic cholecystectomy presented PPP one year later (20). Laparoscopic cholecystectomy has lower incidence of PPP when compared to open technique (19, 21). In our study, laparoscopic cholecystectomy presented the lowest incidence of PPP (8.3%), which could be explained by the use of the laparoscopic technique. Nerve injury is considered one of the most important factors for PPP development, and consequently nerve sparing techniques should reduce the incidence of PPP (1). The other groups of surgery studied in our sample are all open techniques, where incidence of nerve injury is higher.

On the other hand, TKHR presented the highest percentage of PPP development. Research has highlighted that PPP after joint replacement is a considerable problem, affecting between 13.1% to 44.4% of total knee replacement patients (22, 23) and 8.1% to 28.1% of total hip replacement patients (24, 25). Joint replacement is a classic example where PPP can be a consequence of a surgery that was performed to alleviate persistent pain. The high incidence of preoperative pain in these patients could be one of the possible explanations for the higher incidence of PPP in our sample.

Preoperative pain is known to be a risk factor for the development of PPP (26, 27). In our sample, patients submitted to joint replacement presented preoperative pain more often (65.0% vs. 17.9%, P < 0.001). Acute postoperative pain, depression, and the number of pain problems elsewhere are other risk factors described for PPP after TKHR (28). However, in our study we were unable to find those associations for TKHR alone.

The majority of our patients with PPP evaluated their average pain severity as mild. However, an important percentage of patients considered it moderate, which should not be neglected as this pain was associated with significant interference in their daily lives.

It is noteworthy that 79.1% of our patients with PPP have some kind of interference in their general activity, with the majority referring a severe interference. These patients also had a significant interference in mood, walking ability, normal work (including both work outside the home and housework), relations with other people, sleep, and enjoyment of life. This interference, besides its individual and social consequences in terms of reduced QoL and suffering, will be responsible for subsequent costs to the health care and social support systems of our societies (4, 29, 30).

Among the different groups of surgeries, we failed to detect differences related to severity and interference. However, future studies with larger samples may detect it.

With respect to preoperative risk factors, our study is in accordance with the evidence that preoperative pain is a predictor for PPP, which might reflect an independent risk factor, but could also be a manifestation of predisposing factors (26, 27, 29). Our study results suggest that higher pain severity is associated with higher incidence of PPP.

The history of prior surgery in the related area could be indirectly responsible for the development of PPP, because previous surgery in the related area was associated with the existence of preoperative pain.

Regarding postoperative risk factors, acute postoperative pain was associated with the development of PPP, which was already described in other studies. Poorly relieved acute pain is commonly mentioned as a striking risk factor in PPP development (31). Our findings are in agreement with the existence of a link between the presence of acute postoperative pain or its severity and the development of PPP. Several prospective studies have also underscored the link between the severity of acute pain and PPP (26, 31, 32).

With respect to QoL, our results are in accordance with previous findings that patients who develop PPP have lower QoL after open inguinal hernia repair (33) and mastectomy (34). Pain with significant interference, as PPP was described by our sample, not surprisingly reflects lower QoL.

The subject of depression and anxiety in pain has been extensively described over several decades of pain research and treatment (35). Depression prevalence rates in patients with persistent pain seem to be higher than in the general population and also seem to be more common than among other chronic illness populations, including patients with cardiac disease, cancer, diabetes, and neurologic disorders (36). It was believed that persistent pain is more likely to lead to depression, and patients with more severe, frequent, and enduring pain are at risk for more severe depression (37). However, persistent pain conditions and depression are heterogeneous. In certain pain conditions (e.g., osteoarthritis and rheumatoid arthritis), persistent pain is believed to be more strongly linked to peripheral factors (e.g., cartilage damage, inflammation) and psychosocial factors are considered to be less important. On the other hand, in other pain conditions (e.g., fibromyalgia, irritable bowel syndrome), persistent pain is believed to be more strongly linked to changes in the central nervous system (altered central processing) and psychosocial factors are considered to play a major role (35).

Anxiety and depression disorders are usually correlated with PPP. In 2009, a systematic review of the psychosocial factors related to PPP identified depression, psychological vulnerability, stress, and late return to likely be correlated with PPP (38). In our study, we failed to detect the association between anxiety or depression, measured initially with EQ-5D, and the development of PPP. However, patients under preoperative treatment with benzodiazepines or antidepressants had higher incidence of PPP. For obvious reasons, patients undergoing these treatments have problems related to anxiety and depression. Therefore, our results may suggest that the presence of anxiety and depression problems is a risk factor for developing PPP. At the same time, our results indicate that anxiety and depression can also be seen as consequences of PPP development, because patients without anxiety and depression problems prior to surgery who develop PPP had higher incidence of anxiety and depression problems.

The treatment of pain is an important issue for every health professional and organization. There are some studies that evaluate the treatment of chronic pain in Portugal (39-42), but to our knowledge, this is the first study that evaluates the specific follow-up and treatment of PPP in Portugal. There is urgent need for more research about the treatment of PPP, because very few studies have addressed it (43). In our sample, almost half of the patients with PPP (including one-third of patients with moderate to severe PPP) did not receive any treatment for their condition, a finding that should be emphasized. The worst pain considered to be moderate and severe was untreated in a very high percentage of patients, which should also be considered. Many of these patients are not treated because they are lost after discharge from hospital.

Some authors suggest that Acute Pain Services should provide an opportunity for consultation regarding continuing pain and have an important role in assessing PPP as an outcome of surgery (43). Recently, it has been reported that telephone consultation partially based on a cognitive-behavioral approach significantly reduced the intensity of pain and improved the QoL in patients with chronic pain in Japan (44). Many PPP patients will seek help from general practitioners, and therefore this group is in need of awareness and training about PPP.

Although there is limited evidence for treatment of PPP, the therapeutic scale according to the world health organization should be followed. Other professionals involved in the care of surgical patients should also be aware of this entity and refer these patients to Pain Units whenever they cannot deal with their treatment. It should be noted that it is an ethical duty to treat these patients, and that patients under treatment refer a significant improvement in symptoms.

Our sample comes from a single hospital, which could cause some bias with respect to the usual acute pain care. Our Acute Pain Unit works 24 hours per day, every day of the week, and provides acute pain care according to recommended standards.

Recently, there has been an appeal to conduct procedure-specific studies that evaluate the development of PPP. However, we selected some groups of procedure-specific surgeries in order to gain a global view of PPP in our hospital, and with that we obtained small procedure-specific groups.

To conclude, this study characterizes the problem of PPP after several types of surgery and enounces some of its associated factors and consequences. Our results emphasize the lack of identification and treatment of PPP, which should constitute a warning to health professionals and authorities involved in the treatment of postoperative pain.

Acknowledgments

We thank all of the members of the post-anesthesia care unit involved in the field work. We also gratefully acknowledge all of the study participants for their collaboration.

Footnotes

Author Contribution:Luis Guimaraes-Pereira and Fernando Abelha developed the protocol. Luis Guimaraes-Pereira, Ines Valdoleiros and Pedro Reis performed the data collection and clinical evaluations. Pedro Reis and Fernando Abelha performed the data analysis. Luis Guimaraes-Pereira wrote the first draft of the paper. Fernando Abelha revised the manuscript. All authors discussed the results and commented on the manuscript. All authors have read and approved this paper.

References

  • 1.Kehlet H, Edwards RR, Buvanendran A. Persistent postoperative pain: Pathogenic mechanisms and preventive strategies. Seattle: International Association for the Study of Pain; 2012. [Google Scholar]
  • 2.Crombie IK, Davies HT, Macrae WA. Cut and thrust: antecedent surgery and trauma among patients attending a chronic pain clinic. Pain. 1998;76(1-2):167–71. [PubMed] [Google Scholar]
  • 3.Jenkins JT, O'Dwyer PJ. Inguinal hernias. BMJ. 2008;336(7638):269–72. doi: 10.1136/bmj.39450.428275.AD. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Blyth FM, March LM, Cousins MJ. Chronic pain-related disability and use of analgesia and health services in a Sydney community. Med J Aust. 2003;179(2):84–7. doi: 10.5694/j.1326-5377.2003.tb05441.x. [DOI] [PubMed] [Google Scholar]
  • 5.Johansen A, Romundstad L, Nielsen CS, Schirmer H, Stubhaug A. Persistent postsurgical pain in a general population: prevalence and predictors in the Tromso study. Pain. 2012;153(7):1390–6. doi: 10.1016/j.pain.2012.02.018. [DOI] [PubMed] [Google Scholar]
  • 6.Azevedo LF, Costa-Pereira A, Mendonca L, Dias CC, Castro-Lopes JM. Epidemiology of chronic pain: a population-based nationwide study on its prevalence, characteristics and associated disability in Portugal. J Pain. 2012;13(8):773–83. doi: 10.1016/j.jpain.2012.05.012. [DOI] [PubMed] [Google Scholar]
  • 7.DGS D-GoH. Strategic plan for prevention and control of pain. Portugal: 2013. [Google Scholar]
  • 8.Becker N, Bondegaard Thomsen A, Olsen AK, Sjogren P, Bech P, Eriksen J. Pain epidemiology and health related quality of life in chronic non-malignant pain patients referred to a Danish multidisciplinary pain center. Pain. 1997;73(3):393–400. doi: 10.1016/S0304-3959(97)00126-7. [DOI] [PubMed] [Google Scholar]
  • 9.Kemler MA, de Vet HC. Health-related quality of life in chronic refractory reflex sympathetic dystrophy (complex regional pain syndrome type I). J Pain Symptom Manage. 2000;20(1):68–76. doi: 10.1016/s0885-3924(00)00170-6. [DOI] [PubMed] [Google Scholar]
  • 10.Azevedo LF, Pereira AC, Dias C, Agualusa L, Lemos L, Romao J. Translation, Adaptation and Cultural Multicenter Validation Instrument for Screening and Chronic Pain Impact Assessment. Dor; 2007. [Google Scholar]
  • 11.Cleeland CS, Ryan KM. Pain assessment: global use of the Brief Pain Inventory. Ann Acad Med Singapore. 1994;23(2):129–38. [PubMed] [Google Scholar]
  • 12.Keller S, Bann CM, Dodd SL, Schein J, Mendoza TR, Cleeland CS. Validity of the brief pain inventory for use in documenting the outcomes of patients with noncancer pain. Clin J Pain. 2004;20(5):309–18. doi: 10.1097/00002508-200409000-00005. [DOI] [PubMed] [Google Scholar]
  • 13.Pinto PR, McIntyre T, Nogueira-Silva C, Almeida A, Araujo-Soares V. Risk factors for persistent postsurgical pain in women undergoing hysterectomy due to benign causes: a prospective predictive study. J Pain. 2012;13(11):1045–57. doi: 10.1016/j.jpain.2012.07.014. [DOI] [PubMed] [Google Scholar]
  • 14.Melzack R. The short-form McGill pain questionnaire. Pain. 1987;30(2):191–7. doi: 10.1016/0304-3959(87)91074-8. [DOI] [PubMed] [Google Scholar]
  • 15.Brooks R, Rabin R, De Charro F. The measurement and valuation of health status using EQ-5D: a European perspective: evidence from the EuroQol BIOMED Research Programme. Springer Science & Business Media; 2013. [Google Scholar]
  • 16.Ferreira PL, Ferreira LN, Pereira LN. [Contribution for the validation of the Portuguese version of EQ-5D]. Acta Med Port. 2013;26(6):664–75. [PubMed] [Google Scholar]
  • 17.Searle RD, Simpson KH. Chronic post-surgical pain. Continu Educ Anaesth Crit Care Pain. 2010;10(1):12–4. doi: 10.1093/bjaceaccp/mkp041. [DOI] [Google Scholar]
  • 18.Bruehl S, Burns JW, Gupta R, Buvanendran A, Chont M, Kinner E, et al. Endogenous opioid function mediates the association between laboratory-evoked pain sensitivity and morphine analgesic responses. Pain. 2013;154(9):1856–64. doi: 10.1016/j.pain.2013.06.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Perkins FM, Kehlet H. Chronic pain as an outcome of surgery. A review of predictive factors. Anesthesiology. 2000;93(4):1123–33. doi: 10.1097/00000542-200010000-00038. [DOI] [PubMed] [Google Scholar]
  • 20.Jess P, Jess T, Beck H, Bech P. Neuroticism in relation to recovery and persisting pain after laparoscopic cholecystectomy. Scand J Gastroenterol. 1998;33(5):550–3. doi: 10.1080/00365529850172151. [DOI] [PubMed] [Google Scholar]
  • 21.Stiff G, Rhodes M, Kelly A, Telford K, Armstrong CP, Rees BI. Long-term pain: less common after laparoscopic than open cholecystectomy. Br J Surg. 1994;81(9):1368–70. doi: 10.1002/bjs.1800810939. [DOI] [PubMed] [Google Scholar]
  • 22.Brander VA, Stulberg SD, Adams AD, Harden RN, Bruehl S, Stanos SP, et al. Predicting total knee replacement pain: a prospective, observational study. Clin Orthop Relat Res. 2003;(416):27–36. doi: 10.1097/01.blo.0000092983.12414.e9. [DOI] [PubMed] [Google Scholar]
  • 23.Puolakka PA, Rorarius MG, Roviola M, Puolakka TJ, Nordhausen K, Lindgren L. Persistent pain following knee arthroplasty. Eur J Anaesthesiol. 2010;27(5):455–60. doi: 10.1097/EJA.0b013e328335b31c. [DOI] [PubMed] [Google Scholar]
  • 24.Nikolajsen L, Brandsborg B, Lucht U, Jensen TS, Kehlet H. Chronic pain following total hip arthroplasty: a nationwide questionnaire study. Acta Anaesthesiol Scand. 2006;50(4):495–500. doi: 10.1111/j.1399-6576.2006.00976.x. [DOI] [PubMed] [Google Scholar]
  • 25.Singh JA, Lewallen D. Predictors of pain and use of pain medications following primary Total Hip Arthroplasty (THA): 5,707 THAs at 2-years and 3,289 THAs at 5-years. BMC Musculoskelet Disord. 2010;11:90. doi: 10.1186/1471-2474-11-90. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Kehlet H, Jensen TS, Woolf CJ. Persistent postsurgical pain: risk factors and prevention. Lancet. 2006;367(9522):1618–25. doi: 10.1016/S0140-6736(06)68700-X. [DOI] [PubMed] [Google Scholar]
  • 27.Macrae WA. Chronic post-surgical pain: 10 years on. Br J Anaesth. 2008;101(1):77–86. doi: 10.1093/bja/aen099. [DOI] [PubMed] [Google Scholar]
  • 28.Wylde V, Hewlett S, Learmonth ID, Dieppe P. Persistent pain after joint replacement: prevalence, sensory qualities, and postoperative determinants. Pain. 2011;152(3):566–72. doi: 10.1016/j.pain.2010.11.023. [DOI] [PubMed] [Google Scholar]
  • 29.Schnabel A, Pogatzki-Zahn E. [Predictors of chronic pain following surgery. What do we know?]. Schmerz. 2010;24(5):517–31. doi: 10.1007/s00482-010-0932-0. quiz 532-3. [DOI] [PubMed] [Google Scholar]
  • 30.Miladinia M, Baraz S, Shariati A, Malehi A, Amadzadeh A. Relationship Between Chronic Pain and Quality of Life in Patients With Acute Leukemia Undergoing Chemotherapy. Jundishapur J Chron Dis Care. 2015;4(3) [Google Scholar]
  • 31.Lavand’homme P. The progression from acute to chronic pain. Curr Opinion Anaesthesiol. 2011;24(5):545–50. doi: 10.1097/ACO.0b013e32834a4f74. [DOI] [PubMed] [Google Scholar]
  • 32.Katz J, Seltzer Z. Transition from acute to chronic postsurgical pain: risk factors and protective factors. Expert Rev Neurother. 2009;9(5):723–44. doi: 10.1586/ern.09.20. [DOI] [PubMed] [Google Scholar]
  • 33.Poobalan AS, Bruce J, King PM, Chambers WA, Krukowski ZH, Smith WC. Chronic pain and quality of life following open inguinal hernia repair. Br J Surg. 2001;88(8):1122–6. doi: 10.1046/j.0007-1323.2001.01828.x. [DOI] [PubMed] [Google Scholar]
  • 34.Macdonald L, Bruce J, Scott NW, Smith WC, Chambers WA. Long-term follow-up of breast cancer survivors with post-mastectomy pain syndrome. Br J Cancer. 2005;92(2):225–30. doi: 10.1038/sj.bjc.6602304. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Campbell LC, Clauw DJ, Keefe FJ. Persistent pain and depression: a biopsychosocial perspective. Biol Psychiatry. 2003;54(3):399–409. doi: 10.1016/s0006-3223(03)00545-6. [DOI] [PubMed] [Google Scholar]
  • 36.Banks SM, Kerns RD. Explaining high rates of depression in chronic pain: A diathesis-stress framework. Psychol Bull. 1996;119(1):95–110. doi: 10.1037/0033-2909.119.1.95. [DOI] [Google Scholar]
  • 37.Fishbain DA, Cutler R, Rosomoff HL, Rosomoff RS. Chronic pain-associated depression: antecedent or consequence of chronic pain? A review. Clin J Pain. 1997;13(2):116–37. doi: 10.1097/00002508-199706000-00006. [DOI] [PubMed] [Google Scholar]
  • 38.Hinrichs-Rocker A, Schulz K, Jarvinen I, Lefering R, Simanski C, Neugebauer EA. Psychosocial predictors and correlates for chronic post-surgical pain (CPSP) - a systematic review. Eur J Pain. 2009;13(7):719–30. doi: 10.1016/j.ejpain.2008.07.015. [DOI] [PubMed] [Google Scholar]
  • 39.Azevedo LF, Costa-Pereira A, Mendonca L, Dias CC, Castro-Lopes JM. A population-based study on chronic pain and the use of opioids in Portugal. Pain. 2013;154(12):2844–52. doi: 10.1016/j.pain.2013.08.022. [DOI] [PubMed] [Google Scholar]
  • 40.Azevedo LF, Costa-Pereira A, Mendonca L, Dias CC, Castro-Lopes JM. Chronic pain and health services utilization: is there overuse of diagnostic tests and inequalities in nonpharmacologic treatment methods utilization? Med Care. 2013;51(10):859–69. doi: 10.1097/MLR.0b013e3182a53e4e. [DOI] [PubMed] [Google Scholar]
  • 41.Figueiredo R, Sousa M, Miguel C, Simoes E. [Analgesic prescription habits in a population of patients with chronic rheumatic disease]. Acta Med Port. 2011;24(1):53–8. [PubMed] [Google Scholar]
  • 42.Beubler E, Eisenberg E, Castro-Lopes J, Rhodin A. Prescribing policies of opioids for chronic pain. J Pain Palliat Care Pharmacother. 2007;21(2):53–5. [PubMed] [Google Scholar]
  • 43.Kalso E. IV. Persistent post-surgery pain: research agenda for mechanisms, prevention, and treatment. Br J Anaesth. 2013;111(1):9–12. doi: 10.1093/bja/aet211. [DOI] [PubMed] [Google Scholar]
  • 44.Ikemoto K, Yamagata Y, Ikemoto T, Kawai T, Aono S, Arai YC. Telephone Consultation Partially Based on a Cognitive-Behavioral Approach Decreases Pain and Improves Quality of Life in Patients With Chronic Pain. Anesth Pain Med. 2015;5(6):e36461. doi: 10.5812/aapm.32140. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Anesthesiology and Pain Medicine are provided here courtesy of Brieflands

RESOURCES