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*Department of Trauma and Orthopaedic Surgery, Design. This is a prospective cross-sectional study
Cologne-Merheim Medical Center (CMMC), University at a university-affiliated clinic/level 1 trauma center.
of Witten/Herdecke; †Institute for Research in Patients were followed at least 1 year postopera-
Operative Medicine (IFOM), University of tively. By surgical discipline, procedures were
Witten/Herdecke, Cologne, Germany; ‡Clinic of 50% orthopedic/trauma, 33% general (abdominal/
Surgery and Orthopaedics, Kantonales Spital Grabs, visceral), and 17% vascular.
Grabs; §Clinic of Neurosurgery, Kantonsspital St.
Setting. All patients admitted during one year
Gallen, St. Gallen, Switzerland; ¶Biometrics and
(N = 3020) were eligible. Exclusion criteria were cog-
Statistics, Institute for Research in Operative Medicine nitive impairment, communication/language barrier,
(IFOM); **Department of Abdominal, Vascular, and nonoperative treatment, and refusal to participate. A
Transplant Surgery, Cologne Merheim Medical Center CPSP questionnaire was completed. Step-by-step
(CMMC), University of Witten/Herdecke, Cologne, analysis followed with a 2nd questionnaire to detect
Germany CPSP with numeric rating scale (NRS) pain intensity
≥3. Finally, individual follow-up examinations were
Reprint requests to: Christian Johannes Paul performed.
Simanski, MD, Department of Trauma and Orthopedic
Surgery, Cologne-Merheim Medical Center (CMMC), Results. 911 patients responded (30.2%). 522 com-
University of Witten/Herdecke, Ostmerheimerstrasse plained of pain intensity ≥3 on NRS (scale 0–10). The
200, Cologne 51109, Germany. Tel: second step identified 214 patients with chronic
0049-221-8907-13018; Fax: 0049-221-8907-3085; pain (NRS ≥3, mean 29 months postoperatively). On
E-mail: Christian.Simanski@uni-koeln.de. final examination, 83 CPSP patients (14.8%) were
identified. By surgical discipline, 28% were general,
#Both authors contributed equally. 15% vascular, and 57% trauma/orthopedic surgery.
Most oftenly cited pain sites were joint (49.4%),
The authors declare no conflicts of interest in the incisional/scar (37.7%), and nerve pain (33.7%).
publication of this study. By procedure, patients underwent pelvic surgery,
colon surgery, laparoscopies, inguinal herniorrha-
Author’s contributions : CJPS, EAMN, KK, SH, and PH phies, arthroscopies, and hardware extractions. All
developed the study, design, and research. CJPS, patients in the “laborer” and “unemployed” catego-
EAMN, and RL supervised conduction of the study. ries reported chronic pain.
CJPS, KK, SH, PH, and RL collected and managed
the data. CJPS and AA drafted the manuscript, Conclusion. Bias due to study design and/or het-
contributing equally. All other authors contributed erogeneity of patients is possible, but there was a
substantially to its revision. CJPS takes responsibility high CPSP rate after 2 years both generally and
for the paper as a whole. RL provided statistical particularly in orthopedic/trauma (57%) patients.
advice on the study design and analyzed the data Both “major” and “minor” surgical procedures led
along with CJPS, KK, SH, CP-K, and AA. to CPSP.
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Key Words. Risk Factors; Pain Management; hospital, the questionnaire was modified. The study was
Chronic Post-Surgical Pain (CPSP); Persistent Pain; approved by our local ethics committee. All patients were
Prospective Study treated under the conditions of the Helsinki II declaration
and all subjects provided informed consent to partici-
pate. Exclusion criteria were cognitive impairment,
Introduction communication/language barrier in non-native speakers,
non-operative treatment, and refusal to participate. To
The development of chronic postsurgical pain (CPSP) clarify whether the pain reported on the first questionnaire
appears to be a multifactorial process. It is influenced by (mean 19 months post OP, Range: 13–26 months;
physical, psychological, genetic, and social factors [1,2]. SD ± 3.5 months) required further investigation (numerical
Numerous studies have investigated the process of “how rating scale NRS ≥3; scale 0–10), and whether it appeared
acute pain becomes chronic” after various interventions related to surgery, a second analysis was performed by
[2–4]. Multiple surgical procedures within a single periph- examining patient charts and performing telephone inter-
eral nerve distribution lead to high incidence of CPSP views (Figure 1). Thus, we differentiated patients treated
[2,3]. Patients complain of CPSP in 5–65% after thora- operatively versus non-operatively, and whether a nonex-
cotomy [5,6], 30–50% after cardiac surgery [7,8], 5–63% istent, possible, or definite connection between the surgi-
after hernia surgery [9,10], 11–57% after mastectomy cal intervention and current pain symptoms was present.
[11,12], and 30–85% after amputations [13]. Quoted rates Patients with possible or definite chronic pain related to
of incidence for CPSP vary widely, depending on study surgery were invited to return to our clinic where a follow
design, single or multi center participation, clinic level of up examination was performed to assess the symptoms
care, surgical expertise, etc. Severe acute postoperative of CPSP (mean 29 months post OP, Range: 24–35
pain seems to be a risk factor for the development of months; SD ± 3.5 months).
chronic pain [3,4]. In more than 115,000 patients,
Gerbershagen et al. found that very high pain intensity on Definition of CPSP
the first postoperative day was reported after “minor”
interventions, e.g. appendectomy, cholecystectomy, hem- We defined CPSP similarly to Macrae [20]: 1) Pain that
orrhoidectomy, and tonsillectomy, as well as after major develops after surgery, 2) where other etiologies have
orthopedic surgery [14]. Analysis of the literature con- been ruled out, and 3) exacerbation of a pre-existing
firmed high incidence rates of CPSP after these proce- problem as cause for the pain has been ruled out. Unlike
dures [15–17]. Macrae, we defined CPSP as postoperative pain lasting
longer than 12 months, according to recommendations of
In many studies patients were recruited from tertiary other sources [21].
centers with specialized surgeons, or pain intensities were
measured only on the first postoperative day [14]. It is thus Evaluation
possible that the results exhibit bias, and do not reflect
actual CPSP incidence. In addition, it is important to Evaluation of the questionnaires, telephone interviews, and
examine such rates in the general surgical departments of physical examinations was primarily descriptive. Percent-
primary and secondary care centers, since in our nation at ages refer to the total number of patients with pain requiring
least, patients are generally treated there and not in spe- intervention, i.e. with intensities on VAS/NRS ≥3 (scale
cialized surgical centers [18,19]. The aim of this study was 0–10 where 0 = no pain, 10 = maximum imaginable pain)
to determine the incidence of chronic postoperative pain [22]. Differences in frequency were tested with the Fisher’s
(CPSP) in a general surgical patient population of an aca- exact test, and ranking with the Mann-Whitney U test
demic university-affiliated hospital, and to analyze this (P < 0.05). Analysis was carried out using the SPSS soft-
data for specific contributing factors. ware package (version 17.0, SPSS Inc., Chicago, Ill.,
United States).
Patients and Methods
Standardized Pain Measurement, Documentation,
For this cross-sectional study, we included all 3,020 and Therapy
patients admitted to our facility (vascular, abdominal/
visceral, orthopedic/trauma) over a one year period An independent “study nurse” explained the study back-
(1st August until 31st July). Relative to surgical specia- ground and benefits of the routine daily pain measurement
lity, the patient distribution was 50% undergoing or and documentation procedures to all patients. The routine
thopedic/trauma, 33% abdominal/visceral, and 17% vas- clinical documentation of pain intensity comprised assess-
cular procedures. ments at least twice daily (morning and evening) using a
visual analog scale (VAS, 0–10) at rest and with movement
Development of the Questionnaire (0 = no pain, 10 = worst pain imaginable) [23]. Pain
measurement on weight bearing was performed during
The questionnaire was tested for comprehensiveness, physiotherapy or mobilization on the hospital floor,
clarity, and completion time with a first draft in our clinic and included coughing, stair climbing, or standing for
during a pilot phase of the study. After extensive discus- more than 30 minutes. The VAS pain intensity scores
sions by the “integrated acute pain working group” of our were documented by the responsible nursing staff on
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Pain No pain
NRS-pain intensity ≥3 pts. NRS-pain intensity <3 pts.:
n = 522 n = 389
Pain Pain
Pain
- unclear reason
+ - unclear reason TP 2: Ø 29
n=337 n = 185 months
n = 16 post OP
No
CPSP
n = 83
Chronic pain
n = 115
pain Pain
- unclear reason
+
n= 123
25.9% 35.8% 38.3% n =201
postoperative days 1, 2, 3, 5, 7, 9, 12, 15, 20, 25, 30, and NRS ≥3, and 389 patients (42.7%) reported a NRS <3.
the day of discharge. Standardized pain therapy and pain The analysis of second questionnaire showed the same
management were based on the national guidelines [24] rate of incidence (57.3%), 337 patients reported NRS ≥3
and available standards for each surgical discipline. Addi- after an average period of 29 months postoperatively
tional pharmacologic intervention was included if the VAS (range 24–35 months, SD ± 3.5 months) (Figure 1). More
intensity was ≥3, or held by explicit request of patients, i.e. women than men showed chronic pain symptoms.
“pain acceptance” [22,25]. 51.8% of the CPSP patients (N = 43) and 58.3% of the
chronic pain patients (N = 67) were of female gender.
Results The distribution of the 321 “pain patients” (NRS ≥3)
according to the surgical discipline showed that more
All patients admitted to our general surgical university- than 55% of the trauma/ orthopedic patients suffered
affiliated clinic over the period of one year (N = 3,020) chronic pain (CP) and more than 57% of that group suf-
were questioned about the course of postoperative pain fered CPSP (Tables 2 and 3). After follow-up examina-
by follow up over an average of 19 months (SD ± 3.5 tion, 83 (14.8%) patients exhibited CPSP (Figure 1 and
months). 911 questionnaires were fully completed Table 1), and in 16 patients the relationship between the
(response rate 30.2%). Slightly more men (52.8%) than chronic pain symptoms and the surgical procedure was
women (47.2%) responded. The mean age of patients unclear (e.g., burning pain with projection into the ingui-
was 54 years (±17.6 years). The female average was 5 nal region in a post-herniorrhaphy patient with coexisting
years older than that of males (56.7 versus 51.7 years). coxarthrosis). These latter patients were referred to a
355 patients (39%) estimated their current state of health specialized pain clinic for further workup and treatment.
as “not so good” or “bad”. 665 patients (73%) reported 71.6% of patients in the CPSP group self-reported “not
“improved” or “unchanged” activities of daily living post- so good” and “bad” rates to describe their health status
operatively. Analysis of the initial questionnaire showed highest compared to the “chronic pain” and the “No
that 522 patients (57.3%) reported a pain intensity on pain” group (Table 4). The patients reporting CPSP, later
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confirmed on follow-up examination, underwent various ployed” reported pain on NRS ≥3 more than 1 year after
interventions (Tables 1 and 2). Finally, the distribution of surgery. However, analysis of this social parameter within
CPSP patients according to surgical discipline was 28% the 6 months preceding the second questionnaire
general (abdominal/visceral) surgery, 15% vascular showed, almost 72% (N = 231 of 321) of the respon-
surgery and 57% trauma/orthopedic surgery. When dents had yet returned to work or were retired, 22%
asked for the localization of pain (multiple answers pos- (N = 71) were temporarily incapable of working, and 6%
sible), the most frequent response was joints/lower (N = 19) were signed off work permanently. Analyzing
extremities and back (Figure 2). The majority of the ethnic factors, 90% of patients were born in our country
patients was married (61.7%) and retired (Figure 3). All and of Caucasian race. According to responses by
patients who reported themselves as “laborer” or “unem- CPSP patients (multiple answers possible) over the
Trauma/
Surgical discipline General (visceral/ abdominal) Vascular orthopedic
Lap = laparoscopy; Hern. repair = hernial repair; Ing.hern.rep. = inguinal hernia repair; Arthrosc. = arthroscopy; Poly. = polytrauma;
CPSP = chronic post surgical pain.
Table 3 Patient-distribution related to the surgical discipline after the second questionnaire, mean 29
months postoperatively (range 24–35 months, SD 3.5 months)
CPSP = chronic post surgical pain; CP = chronic pain independent from the surgical site; SD = standard deviation.
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Percentage
ø29 months postoperatively)
“Excellent” .8% 0% 0%
“Very good” 4.2% 0% 1.8%
“Not so good” 41.7% 59.3% 50%
“Bad” 4.2% 12.3% 16.7%
Σ = “Not so good”/“Bad” 45.9% 71.6% 66.7%
N= 120 81 114 Occupation
CPSP = chronic post surgical pain; CP = chronic pain indepen- Figure 3 Demographic data by occupation (N =
dent from the surgical site.
337 patients).
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[29]. Patients reported joint pain (49.4%), incisional pain In the CPSP group, 11% were polytraumatized patients,
(37.7%), and nerve pain (33.7%) more than one year after requiring multiple operations. A recent study confirmed a
surgery (multiple answers possible, Figure 4). A recent correlation between CPSP and the need for a 2nd proce-
systematic review confirmed incisional pain and dure after mastectomy [44]. Other authors have also
neuropathic pain as major causes of CPSP [31]. This is reported high rates of CPSP in patients after trauma
often associated with an intraoperative nerve injury or surgery [28].
resection [9,32] and a potentially avoidable complication.
Töns and Schumpelick showed less neuropathic pain Study Limitations
after nerve and soft tissue protection was implemented
during inguinal herniorrhaphy [3,33]. Other studies have The study design did not enable collection of patient data
confirmed that postoperative incisional pain can become regarding preoperative health and pain status. We
chronic. Wilder-Smith showed that the pain threshold for achieved a questionnaire response rate of only 30.2%;
perception of painful stimuli is reduced during revision thus, selection bias cannot be excluded. Although every
procedures (e.g. scar revisions, neuroma resections), patient was treated using our facility specific multimodal
causing allodynia [34]. Furthermore, not only is mechani- pain policies, and pain scores were documented using a
cally induced neuropathy important, but there is also a role specific documentation system, in some cases documen-
for inflammatory immunological components. Post- tation of the pain intensity was incomplete. We collected
surgical inflammatory neuropathy was found histologically data for over 2 years postoperatively (29 months ± 3.5
via nerve biopsy in 21 nerves resected from CPSP months), but the range of follow up dates was wide,
patients, regardless of the presence of mechanical injury complicated by the difficulties in making follow up
[35]. The most consistent risk factor for CPSP is severe appointments. The follow-up physical examination identi-
acute postoperative pain [3,4,9,36,37]. It is hypothesized fied 83 CPSP patients, but after the 3 patient interviews,
that persistent peripheral nociceptive input from injured we also confirmed that 123 patients did not experience
nerves causes neuroplastic changes in the CNS, resulting chronic pain. The physical examination identified 16 cases
in nervous hyperexcitability [4,36]. Some authors have in whom the origin of chronic pain was unclear; these
reported that use of intraoperative nerve blocks in proce- patients were referred to a special pain clinic.
dures known to cause severe postoperative pain (e.g.
thoracotomy) significantly decrease pain up to 6 months Conclusion
postoperatively [38,39]. Thus, interdisciplinary pain man-
agement allows use of additional regional anesthetic mea- This study confirms a high incidence of CPSP of 14.8%
sures with the goal of disrupting this acute to chronic more than 2 years postoperatively. Despite standardized
transformation mechanism [40]. Our patients received pain therapy algorithms in our facility, one in three patients
postoperative pain therapy according to standardized experienced severe postoperative pain requiring further
national S3 guidelines, specific to each surgical discipline intervention (VAS/NRS ≥3). The rate of patients developing
[24]. In an analysis of more than 115,000 patients under- CPSP after trauma or orthopedic procedures was high
going 179 surgical procedures, Gerbershagen et al. (57%), but because of our study design, selection bias
reported that high intensity postoperative pain is often cannot be excluded. The CPSP patients evaluated their
reported after “minor” interventions (e.g., appendectomy, pain as chronic incisional, articular, or neuropathic pain.
1227
Thus, our analysis focused on these pain types. An 12 Tasmuth T, Estlanderb AM, Kalso E. Effect of present
iatrogenic nerve lesion/therapeutic resection is a poten- pain and mood on the memory of past postoperative
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laparoscopies, arthroscopies, hardware extractions, etc.) 13 Hanley MA, Jensen MP, Smith DG, et al.
can also cause CPSP. Social factors may play a role in the Preamputation pain and acute pain predict chronic
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intensity (NRS ≥3) more than 1 year after surgery.
14 Gerbershagen HJ, Aduckathil S, van Wijck AJ, et al.
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