UI - 22510214
PMID- 12623915
DA - 20030307
DCOM- 20030402
IS - 1468-5833
VI - 326
IP - 7388
DP - 2003 Mar 8
TI - 10-minute consultation: chronic low back pain.
PG - 535
AD - Department of Rheumatology, Leicester Royal Infirmary, Leicester LE1 5WW.
FAU - Samanta, Jo
AU - Samanta J
FAU - Kendall, Julia
AU - Kendall J
FAU - Samanta, Ash
AU - Samanta A
LA - eng
PT - Journal Article
PT - Review
PT - Review, Tutorial
CY - England
TA - BMJ
JID - 8900488
SB - AIM
SB - IM
MH - Human
MH - Low Back Pain/*etiology/psychology/therapy
MH - Medical History Taking
MH - Physical Examination
MH - Referral and Consultation
MH - Risk Factors
RF - 0
EDAT- 2003/03/08 04:00
MHDA- 2003/04/04 05:00
AID - 10.1136/bmj.326.7388.535 [doi]
AID - 326/7388/535 [pii]
PST - ppublish
SO - BMJ 2003 Mar 8;326(7388):535.


UI - 22502364
PMID- 12616183
DA - 20030304
IS - 0749-8047
VI - 19
IP - 2
DP - 2003 Mar-Apr
TI - Pain catastrophizing and symptom severity during upper respiratory tract
illness.
PG - 125-33
AB - OBJECTIVES The present study examined the relation of pain catastrophizing
to the severity of upper respiratory tract illness.MATERIALS AND METHODS
Participants included 50 adults (35 female subjects, 15 male) who were
self-diagnosed with upper respiratory tract illness and who agreed to
complete a diary of symptoms for 7 days. Illness symptoms were grouped
into three categories: pain-related, constitutional, and respiratory
symptoms.RESULTS Results showed that pain catastrophizing was associated
with symptom number and symptom severity in all three categories of
symptoms. The rumination subscale of the Pain Catastrophizing Scale showed
the strongest relations with illness severity. The relation between pain
catastrophizing and illness severity remained significant even when
controlling for initial symptom severity, duration of the symptoms before
the study period, and depression.DISCUSSION The results provide the
preliminary evidence that the influence of pain catastrophizing may not be
restricted to pain-specific domains. The data also provide some support
for the view that the excessive focus on bodily sensations may account for
more severe symptoms.
FAU - Devoulyte, Kristina
AU - Devoulyte K
FAU - Sullivan, Michael J L
AU - Sullivan MJ
LA - eng
PT - Journal Article
CY - United States
TA - Clin J Pain
JID - 8507389
SB - IM
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
PST - ppublish
SO - Clin J Pain 2003 Mar-Apr;19(2):125-33.


UI - 22502363
PMID- 12616182
DA - 20030304
IS - 0749-8047
VI - 19
IP - 2
DP - 2003 Mar-Apr
TI - Pain on injection of propofol: the effect of granisetron pretreatment.
PG - 121-4
AB - OBJECTIVE To assess the effect of granisetron pretreatment in alleviating
propofol injection pain.STUDY DESIGN A randomized, controlled,
double-blind study, using venous retention with a tourniquet.MATERIALS AND
METHODS One hundred fifty adult patients were randomly assigned to one of
three groups: group 1 (who received 5 mL of 0.9% saline pretreatment),
group 2 (who received 5 mL lidocaine [40 mg in 0.9% saline] pretreatment),
and group 3 (who received 5 mL granisetron [2 mg in 0.9% saline]
pretreatment). Injections were given in the largest vein on the dorsum of
the hand. After 2 minutes, the tourniquet was released and one fourth of
the total calculated dose of propofol (2.5 mg/kg body weight) was
administered and pain assessment was made.RESULTS Lidocaine and
granisetron significantly reduced the incidence and severity of propofol
injection pain more than placebo ( < 0.001). The efficacy of granisetron
in alleviating the pain on injection of propofol was no different from
lidocaine.CONCLUSIONS Granisetron pretreatment may be used to reduce the
incidence of pain on injection of propofol, an advantage added to the
useful prevention of postoperative nausea and vomiting.
FAU - Dubey, Prakash K
AU - Dubey PK
FAU - Prasad, Sureshwar S
AU - Prasad SS
LA - eng
PT - Journal Article
CY - United States
TA - Clin J Pain
JID - 8507389
SB - IM
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
PST - ppublish
SO - Clin J Pain 2003 Mar-Apr;19(2):121-4.


UI - 22502360
PMID- 12616179
DA - 20030304
IS - 0749-8047
VI - 19
IP - 2
DP - 2003 Mar-Apr
TI - Psychologically based occupational rehabilitation: the pain-disability
prevention program.
PG - 97-104
AB - OBJECTIVES To describe the development, implementation, and preliminary
outcome of the Pain-Disability Prevention (PDP) Program. The PDP Program
is a 10-week cognitive-behavioral intervention program that aims to
increase daily involvement in goal-directed activity and minimize
psychological barriers to activity involvement after occupational injury.
Workers' Compensation Board claimants with soft tissue injuries to the
back, who were still off work 6 weeks after injury and showed evidence of
at least one "yellow flag," were offered participation in the PDP
Program.DESIGN A single-group, prospective treatment outcome
analysis.PARTICIPANTS Data from the first 104 claimants who participated
in the PDP Program are summarized.RESULTS Participation in the PDP Program
was associated with a 60% success rate, where success was defined as
return to work (45%) or readiness to return to work (15%). Initial scores
on measures of catastrophizing, fear of movement/reinjury, and depression
afforded 92% correct classification of treatment outcome. Early treatment
changes in catastrophizing and fear of movement/reinjury were also
predictive of treatment outcome.CONCLUSIONS The findings suggest that a
psychologically based activity mobilization program can be an effective
means of yielding reductions in psychological risk factors for
occupational disability. Challenges to program implementation, fidelity to
protocol, and issues related to cost efficacy are discussed.
FAU - Sullivan, Michael J L
AU - Sullivan MJ
FAU - Stanish, William D
AU - Stanish WD
LA - eng
PT - Journal Article
CY - United States
TA - Clin J Pain
JID - 8507389
SB - IM
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
PST - ppublish
SO - Clin J Pain 2003 Mar-Apr;19(2):97-104.


UI - 22502359
PMID- 12616178
DA - 20030304
IS - 0749-8047
VI - 19
IP - 2
DP - 2003 Mar-Apr
TI - Secondary prevention of work-related disability in nonspecific low back
pain: does problem-solving therapy help? A randomized clinical trial.
PG - 87-96
AB - OBJECTIVES Given the individual and economic burden of chronic work
disability in low back pain patients, there is a need for effective
preventive interventions. The aim of the present study was to investigate
whether problem-solving therapy had a supplemental value when added to
behavioral graded activity, regarding days of sick leave and work
status.DESIGN Randomized controlled trial.PATIENTS AND SETTING Employees
who were recently on sick leave as a result of nonspecific low back pain
were referred to the rehabilitation center by general practitioner,
occupational physician, or rehabilitation physician. Forty-five employees
had been randomly assigned to the experimental treatment condition that
included behavioral graded activity and problem-solving therapy (GAPS),
and 39 employees had been randomly assigned to behavioral graded activity
and group education (GAGE).OUTCOME MEASURES Days of sick leave and work
status. Data were retrieved from occupational health services.RESULTS Data
analyses showed that employees in the GAPS group had significantly fewer
days of sick leave in the second half-year after the intervention.
Moreover, work status was more favorable for employees in this condition,
in that more employees had a 100% return-to-work and fewer patients ended
up receiving disability pensions one year after the intervention.
Sensitivity analyses confirmed these results.CONCLUSIONS The addition of
problem-solving therapy to behavioral graded activity had supplemental
value in employees with nonspecific low back pain.
AD - parallel.
FAU - Van Den Hout, Johanna H C
AU - Van Den Hout JH
FAU - Vlaeyen, Johan W S
AU - Vlaeyen JW
FAU - Heuts, Peter H T G
AU - Heuts PH
FAU - Zijlema, Johan H L
AU - Zijlema JH
FAU - Wijnen, Joseph A G
AU - Wijnen JA
LA - eng
PT - Journal Article
CY - United States
TA - Clin J Pain
JID - 8507389
SB - IM
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
PST - ppublish
SO - Clin J Pain 2003 Mar-Apr;19(2):87-96.


UI - 22502358
PMID- 12616177
DA - 20030304
IS - 0749-8047
VI - 19
IP - 2
DP - 2003 Mar-Apr
TI - Early identification of patients at risk of developing a persistent back
problem: the predictive validity of the orebro musculoskeletal pain
questionnaire.
PG - 80-6
AB - OBJECTIVE To test the predictive utility of the Orebro Musculoskeletal
Pain Screening Questionnaire in identifying patients at risk for
developing persistent back pain problems.DESIGN Prospective, where
participants completed the questionnaire and their cases were followed for
6 months to assess outcome with regard to pain, function, and absenteeism
due to sickness.PARTICIPANTS One hundred seven patients, recruited from
seven primary care units.RESULTS Discriminant analyses showed that the
items on the questionnaire were significantly related to future problems.
For absenteeism due to sickness, 68% of the patients were correctly
classified into one of three groups, whereas an even distribution would
have produced 33%. The analyses for function correctly classified 81%, and
for pain 71%, into one of two groups, compared with a chance level of 50%.
A total score analysis demonstrated that a cutoff score of 90 points had a
sensitivity of 89% and a specificity of 65% for absenteeism due to
sickness, and a sensitivity of 74% and a specificity of 79% for functional
ability.CONCLUSIONS The results underscore that psychological variables
are related to outcome 6 months later, and they replicate and extend
earlier findings indicating that the Orebro Screening Questionnaire is a
clinically reliable and valid instrument. The total score was a relatively
good predictor of future absenteeism due to sickness as well as function,
but not of pain. The results suggest that the instrument could be of value
in isolating patients in need of early interventions and may promote the
use of appropriate interventions for patients with psychological risk
factors.
FAU - Linton, Steven J
AU - Linton SJ
FAU - Boersma, Katja
AU - Boersma K
LA - eng
PT - Journal Article
CY - United States
TA - Clin J Pain
JID - 8507389
SB - IM
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
PST - ppublish
SO - Clin J Pain 2003 Mar-Apr;19(2):80-6.


UI - 22502357
PMID- 12616176
DA - 20030304
IS - 0749-8047
VI - 19
IP - 2
DP - 2003 Mar-Apr
TI - Introduction: emerging trends in secondary prevention of back pain
disability.
PG - 77-9
FAU - Sullivan, Michael J L
AU - Sullivan MJ
LA - eng
PT - Editorial
CY - United States
TA - Clin J Pain
JID - 8507389
SB - IM
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
PST - ppublish
SO - Clin J Pain 2003 Mar-Apr;19(2):77-9.


UI - 22509434
PMID- 12622508
DA - 20030307
IS - 0265-0215
VI - 20
IP - 2
DP - 2003 Feb
TI - Alternative application site of transdermal nitroglycerin and the
reduction of pain on propofol injection.
PG - 170-2
FAU - Turan, A
AU - Turan A
FAU - Karamanlioglu, B
AU - Karamanlioglu B
FAU - Memis, D
AU - Memis D
FAU - Pamukcu, Z
AU - Pamukcu Z
LA - eng
PT - Letter
CY - England
TA - Eur J Anaesthesiol
JID - 8411711
SB - IM
EDAT- 2003/03/08 04:00
MHDA- 2003/03/08 04:00
PST - ppublish
SO - Eur J Anaesthesiol 2003 Feb;20(2):170-2.


UI - 22509428
PMID- 12622502
DA - 20030307
IS - 0265-0215
VI - 20
IP - 2
DP - 2003 Feb
TI - Nitrous oxide/oxygen mixture and the prevention of pain during injection
of propofol.
PG - 158-61
AB - BACKGROUND AND OBJECTIVE: The incidence of pain associated with the
injection of propofol still remains a problem. This study sought to
examine the analgesic effects of inhaled nitrous oxide in oxygen on the
prevention of propofol injection pain. METHODS: Nitrous oxide in oxygen
was compared with a lidocaine (20 mg)-propofol mixture and with propofol
alone (control) in a prospective, randomized, observer-blinded study. ASA
I and II patients (n = 135) scheduled for elective surgical procedures
were studied. A standard propofol injection technique and scoring system
to measure the pain on injection was used. RESULTS: Demographic variables
were similar between the study groups. Without analgesia (control) 26 of
45 patients (58%) reported pain on injection compared with 11 of 45
patients (24%) in both the nitrous oxide (95% CI: 14-52%, P = 0.001) and
lidocaine groups (95% CI: 14-52%, P = 0.001). CONCLUSIONS: The inhalation
of a nitrous oxide/oxygen mixture significantly reduces the incidence of
pain during propofol injection. This therapeutic stratagem was as
effective as a lidocaine-propofol mixture.
AD - University College Hospital, Department of Anaesthesia, Galway, Ireland.
dharmon@indigo.ie
FAU - Harmon, D
AU - Harmon D
FAU - Rozario, C
AU - Rozario C
FAU - Lowe, D
AU - Lowe D
LA - eng
PT - Journal Article
CY - England
TA - Eur J Anaesthesiol
JID - 8411711
SB - IM
EDAT- 2003/03/08 04:00
MHDA- 2003/03/08 04:00
PST - ppublish
SO - Eur J Anaesthesiol 2003 Feb;20(2):158-61.


UI - 22228005
PMID- 12243291
DA - 20020923
DCOM- 20030304
IS - 0265-0215
VI - 19
IP - 9
DP - 2002 Sep
TI - Epidural morphine injection after combined spinal and epidural
anaesthesia.
PG - 672-6
AB - BACKGROUND AND OBJECTIVE: Although combined spinal and epidural
anaesthesia is efficient and easy to perform, the technique can be a
double-edged sword having the potential risk that an increased flux of
drugs across the meninges through the hole made in it may lead to severe
adverse effects. The aim was to compare the incidence of adverse events
when an epidural injection of morphine was given after combined spinal and
epidural anaesthesia or after epidural anaesthesia. METHODS: Fifteen
patients had an epidural catheter inserted at the L2-3 interspace, and
then a spinal block administered via the L3-4 interspace. Another 15
patients only had an epidural catheter inserted. After the onset of spinal
or epidural anaesthesia had been confirmed, morphine 2 mg was injected
into the epidural space, and a continuous epidural infusion of morphine
was started. At the end of the operation and at 4, 8 and 12 h after the
administration of epidural morphine and on the next day, the following
variables were examined: blood pressure, heart rate, respiratory rate,
arterial blood-gas analysis, visual analogue scale pain scores,
nausea/vomiting scores, and pruritus scores. RESULTS: In the study
population, the epidural injection of morphine was not associated with a
significantly higher incidence of adverse events when given after spinal
anaesthesia than after epidural anaesthesia. CONCLUSIONS: The adverse
effects associated with epidural morphine given after spinal anaesthesia
did not increase significantly when a 27-G Whitacre needle was used. Thus,
the morphine flux through the meningeal hole into the cerebrospinal fluid
was trivial.
AD - Gifu University School of Medicine, Department of Anesthesiology &
Critical Care Medicine, Gifu City, Japan.
FAU - Takenaka-Hamaya, C
AU - Takenaka-Hamaya C
FAU - Hamaya, Y
AU - Hamaya Y
FAU - Dohi, S
AU - Dohi S
LA - eng
PT - Clinical Trial
PT - Journal Article
PT - Randomized Controlled Trial
CY - England
TA - Eur J Anaesthesiol
JID - 8411711
RN - 0 (Analgesics, Opioid)
RN - 57-27-2 (Morphine)
SB - IM
MH - Aged
MH - Aged, 80 and over
MH - Analgesics, Opioid/*adverse effects/therapeutic use
MH - *Anesthesia, Epidural
MH - *Anesthesia, Spinal
MH - Double-Blind Method
MH - Female
MH - Human
MH - Lower Extremity/surgery
MH - Middle Age
MH - Morphine/*adverse effects/therapeutic use
MH - Nausea/etiology
MH - Pain Measurement
MH - Pain, Postoperative/*prevention & control
MH - Prospective Studies
MH - Pruritus/etiology
MH - Respiratory Insufficiency/etiology
MH - Support, Non-U.S. Gov't
EDAT- 2002/09/24 06:00
MHDA- 2003/03/05 04:00
PST - ppublish
SO - Eur J Anaesthesiol 2002 Sep;19(9):672-6.


UI - 22228004
PMID- 12243290
DA - 20020923
DCOM- 20030304
IS - 0265-0215
VI - 19
IP - 9
DP - 2002 Sep
TI - Epidural combination of ropivacaine with sufentanil for postoperative
analgesia after total knee replacement: a pilot study.
PG - 666-71
AB - BACKGROUND AND OBJECTIVE: We assessed the analgesic efficacy of
postoperative epidural infusions of ropivacaine 0.1 and 0.2% combined with
sufentanil 1 microg mL(-1) in a prospective, randomized, double-blinded
study. METHODS: Twenty-two ASA I-III patients undergoing elective
total-knee replacement were included. Lumbar epidural blockade using
ropivacaine 0.75% was combined with either propofol sedation or general
anaesthesia for surgery. After surgery, the epidural infusion was
commenced. Eleven patients in each group received either an epidural
infusion of ropivacaine 0.1% with 1 microg mL(-1) sufentanil (Group 1) or
ropivacaine 0.2% with 1 microg mL(-1) sufentanil (Group 2) at a rate of
5-9 mL h(-1). All patients had access to intravenous pirinatrimide
(piritramide) via a patient-controlled analgesia (PCA) device. RESULTS:
Motor block was negligible for the study duration in both groups. There
was no significant difference with the 100 mm visual analogue scale (VAS)
scores, with the consumption of rescue analgesia or with patient
satisfaction. Patients in Group 1 experienced significantly less nausea (P
< 0.05) than those in Group 2. Both treatment regimens provided effective
postoperative analgesia with only a minimal use of supplemental opioid
PCA. CONCLUSIONS: We recommend the use of ropivacaine 0.1% with 1 microg
mL(-1) sufentanil for postoperative analgesia after total knee replacement
as it provides efficient pain relief with no motor block of the lower
limbs. In addition, compared with 0.2% ropivacaine with sufentanil, the
mixture reduces local anaesthetic consumption without compromise in
patient satisfaction or VAS scores. Patients even experience less nausea.
AD - University of Cologne, Department of Anaesthesiology and Intensive Care
Medicine, Germany. sandra.kampe@t-online.de
FAU - Kampe, S
AU - Kampe S
FAU - Diefenbach, C
AU - Diefenbach C
FAU - Kanis, B
AU - Kanis B
FAU - Auweiler, M
AU - Auweiler M
FAU - Kiencke, P
AU - Kiencke P
FAU - Cranfield, K
AU - Cranfield K
LA - eng
PT - Clinical Trial
PT - Journal Article
PT - Randomized Controlled Trial
CY - England
TA - Eur J Anaesthesiol
JID - 8411711
RN - 0 (Amides)
RN - 0 (Analgesics, Opioid)
RN - 0 (Anesthetics, Combined)
RN - 0 (Anesthetics, Intravenous)
RN - 0 (Anesthetics, Local)
RN - 302-41-0 (Pirinitramide)
RN - 56030-54-7 (Sufentanil)
RN - 84057-95-4 (ropivacaine)
SB - IM
MH - Aged
MH - Amides/administration & dosage/*therapeutic use
MH - Analgesia, Patient-Controlled
MH - Analgesics, Opioid/therapeutic use
MH - Anesthetics, Combined/*therapeutic use
MH - Anesthetics, Intravenous/administration & dosage/*therapeutic use
MH - Anesthetics, Local/administration & dosage/*therapeutic use
MH - *Arthroplasty, Replacement, Knee
MH - Double-Blind Method
MH - Female
MH - Human
MH - Male
MH - Middle Age
MH - Pain, Postoperative/*drug therapy
MH - Pilot Projects
MH - Pirinitramide/therapeutic use
MH - Sufentanil/administration & dosage/*therapeutic use
MH - Treatment Outcome
EDAT- 2002/09/24 06:00
MHDA- 2003/03/05 04:00
PST - ppublish
SO - Eur J Anaesthesiol 2002 Sep;19(9):666-71.


UI - 22503235
PMID- 12614968
DA - 20030304
IS - 0885-3924
VI - 25
IP - 3
DP - 2003 Mar
TI - For the psychologist treating pain patients.
PG - 294-5
FAU - Heil, John
AU - Heil J
LA - eng
PT - Journal Article
CY - United States
TA - J Pain Symptom Manage
JID - 8605836
SB - IM
SB - N
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
AID - S0885392402007054 [pii]
PST - ppublish
SO - J Pain Symptom Manage 2003 Mar;25(3):294-5.


UI - 22503234
PMID- 12614967
DA - 20030304
IS - 0885-3924
VI - 25
IP - 3
DP - 2003 Mar
TI - Pain management in Hong Kong.
PG - 293-4
FAU - Spiess, Jeffrey L
AU - Spiess JL
LA - eng
PT - Journal Article
CY - United States
TA - J Pain Symptom Manage
JID - 8605836
SB - IM
SB - N
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
AID - S0885392402007066 [pii]
PST - ppublish
SO - J Pain Symptom Manage 2003 Mar;25(3):293-4.


UI - 22503233
PMID- 12614966
DA - 20030304
IS - 0885-3924
VI - 25
IP - 3
DP - 2003 Mar
TI - Managing pain in the elderly.
PG - 292-3
FAU - Ferrell, Betty R
AU - Ferrell BR
LA - eng
PT - Journal Article
CY - United States
TA - J Pain Symptom Manage
JID - 8605836
SB - IM
SB - N
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
AID - S088539240200708X [pii]
PST - ppublish
SO - J Pain Symptom Manage 2003 Mar;25(3):292-3.


UI - 22503228
PMID- 12614961
DA - 20030304
IS - 0885-3924
VI - 25
IP - 3
DP - 2003 Mar
TI - Is patient satisfaction a legitimate outcome of pain management?
PG - 264-75
AB - Though many studies have measured patient satisfaction with pain
management using the American Pain Society (APS) Satisfaction Survey or
its variants, little is known about the relationship among the survey
items, or whether items relate to satisfaction at all. In an effort to
refine the measurement of patient satisfaction, a modified version of the
APS survey, which was given to 787 patients as part of a study of
postoperative pain management in six community hospitals, was subjected to
principal components analysis to determine the survey's empirical
structure. Correlations among the five components found were low; a weak
relationship (r = -0.24) was discovered between pain intensity and
satisfaction. A heuristic model estimated by structural equations analysis
yielded additional insights. Though many items thought to influence
patient satisfaction were not closely related to patient-reported
satisfaction, they indicate important clinical factors relevant to quality
of care, and thus, to continuing quality improvement (CQI) efforts.
Results suggest that satisfaction was influenced by effectiveness of
medication, independent of pain intensity, and by communication. Pain
severity ratings near the time satisfaction was measured were more
influential than earlier ratings.
AD - School of Nursing, University of North Carolina at Chapel Hill, Chapel
Hill, NC, USA
FAU - Carlson, John
AU - Carlson J
FAU - Youngblood, Richard
AU - Youngblood R
FAU - Dalton, Jo Ann
AU - Dalton JA
FAU - Blau, William
AU - Blau W
FAU - Lindley, Celeste
AU - Lindley C
LA - eng
PT - Journal Article
CY - United States
TA - J Pain Symptom Manage
JID - 8605836
SB - IM
SB - N
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
AID - S0885392402006772 [pii]
PST - ppublish
SO - J Pain Symptom Manage 2003 Mar;25(3):264-75.


UI - 22503227
PMID- 12614960
DA - 20030304
IS - 0885-3924
VI - 25
IP - 3
DP - 2003 Mar
TI - Ongoing distress from emotional trauma is related to pain, mood, and
physical function in a primary care population.
PG - 256-63
AB - The relationship of trauma history to physical and emotional functioning
in primary care pain patients was examined. Data were drawn from a mailed
screening questionnaire for a larger study designed to evaluate an
intervention for improving pain management in primary care. Results
indicated that 50.4% of the pain patients reported experiencing at least
one previous emotionally traumatic event. Further, 31% of patients with
trauma history continued to be bothered by that experience. Finally,
patients who continued to be significantly bothered by the trauma reported
more pain, emotional distress, poorer social functioning, and more
difficulty with engaging in their daily activities than did patients with
either no trauma history or who had a trauma history but did not have
bothersome thoughts of the trauma. These preliminary findings suggest that
the experience of trauma alone was not related to additional impairments
in physical and psychosocial functioning. However, the report that one
continued to be bothered by thoughts of a trauma was associated with
greater impairments in functioning.
AD - Department of Psychiatry, Dartmouth-Hitchcock Medical Center, Lebanon, NH,
USA
FAU - Seville, Janette L
AU - Seville JL
FAU - Ahles, Tim A
AU - Ahles TA
FAU - Wasson, John H
AU - Wasson JH
FAU - Johnson, Deborah
AU - Johnson D
FAU - Callahan, Eileen
AU - Callahan E
FAU - Stukel, Therese
AU - Stukel T
LA - eng
PT - Journal Article
CY - United States
TA - J Pain Symptom Manage
JID - 8605836
SB - IM
SB - N
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
AID - S0885392402006462 [pii]
PST - ppublish
SO - J Pain Symptom Manage 2003 Mar;25(3):256-63.


UI - 22503226
PMID- 12614959
DA - 20030304
IS - 0885-3924
VI - 25
IP - 3
DP - 2003 Mar
TI - Pain trajectory of taiwanese with nasopharyngeal carcinoma over the course
of radiation therapy.
PG - 247-55
AB - The purpose of this study was to describe the characteristics and
management of pain among patients with nasopharyngeal carcinoma (NPC)
prior to and during the 7-week course of radiation therapy (RT) in Taiwan.
Twenty-nine men and 11 women with NPC participated in this prospective,
longitudinal study. A modified Brief Pain Inventory was used to assess
pain and its interference with daily activities weekly. Medical records
were reviewed to abstract pain management and disease data. Findings
showed that the pain intensity and pain interference scores escalated
prominently at Week 3 and peaked at Week 5, representing the time course
of RT complications. Pain prior to RT exacerbated the RT-induced mucositis
pain. The pain related to RT for NPC was often severe and undertreated,
and affected swallowing and talking more than sleeping or other general
activities. We recommend interventions to control pain be instituted prior
to Week 3 to minimize the potentiation of subsequent pain.
AD - Department of Biobehavioral Nursing and Health System, University of
Washington, Seattle, WA, USA
FAU - Huang, Hsiu Ying
AU - Huang HY
FAU - Wilkie, Diana J
AU - Wilkie DJ
FAU - Chapman, C Richard
AU - Chapman CR
FAU - Ting, Lai Lei
AU - Ting LL
LA - eng
PT - Journal Article
CY - United States
TA - J Pain Symptom Manage
JID - 8605836
SB - IM
SB - N
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
AID - S0885392402006784 [pii]
PST - ppublish
SO - J Pain Symptom Manage 2003 Mar;25(3):247-55.


UI - 22503223
PMID- 12614956
DA - 20030304
IS - 0885-3924
VI - 25
IP - 3
DP - 2003 Mar
TI - Usability of a Computerized PAINReportIt in the General Public with Pain
and People with Cancer Pain.
PG - 213-24
AB - We examined usability (completion time, acceptability, and completeness of
information) of a computerized format for pain assessment, PAINReportIt.
PAINReportIt is the first interactive software extension of the 1970
McGill Pain Questionnaire. Two hundred thirteen patients experiencing pain
were recruited for this descriptive, comparative study. Subjects used a
Microsoft((R)) Windows 95/98 personal computer with a touch-screen to
complete 1) PAINReportIt, 2) demographic, and 3) acceptability questions.
Qualitative and quantitative data from the study support PAINReportIt as a
feasible method for patients to self-report their pain. Patients completed
the tool in less than 18 minutes on average, answered all sections, and
scored it high regarding acceptability. Improved directions and practice
screens would likely improve patients' independence in completing
PAINReportIt, which would free clinicians to focus direct communication on
more complex pain issues.
AD - School of Nursing, University of Washington, Seattle, WA, USA
FAU - Wilkie, Diana J
AU - Wilkie DJ
FAU - Judge, M Kay M
AU - Judge MK
FAU - Berry, Donna L
AU - Berry DL
FAU - Dell, Jean
AU - Dell J
FAU - Zong, Shiping
AU - Zong S
FAU - Gilespie, Rudy
AU - Gilespie R
LA - eng
PT - Journal Article
CY - United States
TA - J Pain Symptom Manage
JID - 8605836
SB - IM
SB - N
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
AID - S0885392402006383 [pii]
PST - ppublish
SO - J Pain Symptom Manage 2003 Mar;25(3):213-24.


UI - 22503222
PMID- 12614955
DA - 20030304
IS - 0885-3924
VI - 25
IP - 3
DP - 2003 Mar
TI - Effectiveness of palliative day care in improving pain, symptom control,
and quality of life.
PG - 202-12
AB - To evaluate the effectiveness of palliative day care in improving pain,
symptom control, and quality of life (QOL), 120 consecutive new referrals
to five specialist palliative day care centers were recruited into a
prospective comparative study. Fifty-three comparison patients were
identified as those patients receiving usual palliative care services
(home care, inpatient care), but did not attend day care. Patients were
assessed at 3 interviews (baseline, 6-8 weeks, and 12-15 weeks) using
measures of health-related quality of life: McGill Quality of Life
Questionnaire (MQOL) and Palliative Care Outcome Scale (POS). There were
two main analyses: 1) patient demographic data were analyzed using
chi-square (chi(2)), and 2) QOL data were compared, based on distribution
of scores, using the Mann-Whitney test (MQOL and POS), and Wilcoxon Signed
Rank for within group differences (POS data only); P < 0.05 was taken as
significant. The patients were representative of those attending
palliative day care in the UK. At baseline, the day care group were
(non-significantly) worse than the comparison group in the MQOL support
domain (P = 0.065). The comparison group had marginally more severe pain
at baseline (P = 0.053) and more severe symptoms at second assessment (P =
0.025). Both patient groups maintained overall health-related quality of
life during the three months of the study. Palliative day care was not
found to improve overall health-related quality of life. The limitations
of the QOL measures in identifying the effects (patient outcomes) of
palliative day care and the differences between the two patient groups
(age, employment, unequal sample sizes) were limitations of the study and
indicate the need for further research in this area.
AD - Department of Palliative Care and Policy, King's College, University of
London, London, UK
FAU - Goodwin, Danielle M
AU - Goodwin DM
FAU - Higginson, Irene J
AU - Higginson IJ
FAU - Myers, Kathy
AU - Myers K
FAU - Douglas, Hannah Rose
AU - Douglas HR
FAU - Normand, Charles E
AU - Normand CE
LA - eng
PT - Journal Article
CY - United States
TA - J Pain Symptom Manage
JID - 8605836
SB - IM
SB - N
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
AID - S0885392402006887 [pii]
PST - ppublish
SO - J Pain Symptom Manage 2003 Mar;25(3):202-12.


UI - 22503220
PMID- 12614953
DA - 20030304
IS - 0885-3924
VI - 25
IP - 3
DP - 2003 Mar
TI - Herpes zoster. A previously unrecognized complication of epidural steroids
in the treatment of complex regional pain syndrome.
PG - 198-9
AD - Pain Management Clinic Rockyview General Hospital, Calgary, Alberta,
Canada
FAU - Parsons, Simon J
AU - Parsons SJ
FAU - Hawboldt, Geoffrey S
AU - Hawboldt GS
LA - eng
PT - Journal Article
CY - United States
TA - J Pain Symptom Manage
JID - 8605836
SB - IM
SB - N
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
AID - S0885392402007078 [pii]
PST - ppublish
SO - J Pain Symptom Manage 2003 Mar;25(3):198-9.


UI - 22503219
PMID- 12614952
DA - 20030304
IS - 0885-3924
VI - 25
IP - 3
DP - 2003 Mar
TI - Criteria of pain response to radiotherapy in advanced cancer patients.
PG - 197
AD - Department of Oncology Hospital Universitario de Valladolid, Valladolid,
Spain
FAU - Rey, Pilar
AU - Rey P
FAU - Vecino, Amaya
AU - Vecino A
FAU - Rubiales, Alvaro S
AU - Rubiales AS
FAU - Lopez-Lara, Francisco
AU - Lopez-Lara F
LA - eng
PT - Journal Article
CY - United States
TA - J Pain Symptom Manage
JID - 8605836
SB - IM
SB - N
EDAT- 2003/03/05 04:00
MHDA- 2003/03/05 04:00
AID - S0885392402007091 [pii]
PST - ppublish
SO - J Pain Symptom Manage 2003 Mar;25(3):197.


UI - 22508615
PMID- 12621144
DA - 20030306
DCOM- 20030317
IS - 1533-4406
VI - 348
IP - 10
DP - 2003 Mar 6
TI - Analgesics for the treatment of pain in children.
PG - 959-60; author 959-60
FAU - Birenbaum, Debra
AU - Birenbaum D
FAU - Mattison, Donald R
AU - Mattison DR
LA - eng
PT - Comment
PT - Letter
CY - United States
TA - N Engl J Med
JID - 0255562
RN - 0 (Analgesics)
SB - AIM
SB - IM
CON - N Engl J Med. 2002 Oct 3;347(14):1094-103. PMID: 12362012
MH - Analgesics/*therapeutic use
MH - Child
MH - Drug Evaluation/*legislation & jurisprudence
MH - Drug Labeling
MH - Human
MH - Infant
MH - Pain/*drug therapy
MH - United States
MH - United States Food and Drug Administration
EDAT- 2003/03/07 04:00
MHDA- 2003/03/18 04:00
AID - 10.1056/NEJM200303063481020 [doi]
AID - 348/10/959 [pii]
PST - ppublish
SO - N Engl J Med 2003 Mar 6;348(10):959-60; author 959-60.


UI - 22508798
PMID- 12620613
DA - 20030306
IS - 0304-3959
VI - 102
IP - 1-2
DP - 2003 Mar
TI - Cannabis use for chronic non-cancer pain: results of a prospective survey.
PG - 211-6
AB - There has been a surge in interest in medicinal cannabis in Canada. We
conducted a questionnaire survey to determine the current prevalence of
medicinal cannabis use among patients with chronic non-cancer pain, to
estimate the dose size and frequency of cannabis use, and to describe the
main symptoms for which relief was being sought. Over a 6-week period in
mid-2001, 209 chronic non-cancer pain patients were recruited in an
anonymous cross-sectional survey. Seventy-two (35%) subjects reported ever
having used cannabis. Thirty-two (15%) subjects reported having used
cannabis for pain relief (pain users), and 20 (10%) subjects were
currently using cannabis for pain relief. Thirty-eight subjects denied
using cannabis for pain relief (recreational users). Compared to never
users, pain users were significantly younger (P=0.001) and were more
likely to be tobacco users (P=0.0001). The largest group of patients using
cannabis had pain caused by trauma and/or surgery (51%), and the site of
pain was predominantly neck/upper body and myofascial (68% and 65%,
respectively). The median duration of pain was similar in both pain users
and recreational users (8 vs. 7 years; P=0.7). There was a wide range of
amounts and frequency of cannabis use. Of the 32 subjects who used
cannabis for pain, 17 (53%) used four puffs or less at each dosing
interval, eight (25%) smoked a whole cannabis cigarette (joint) and four
(12%) smoked more than one joint. Seven (22%) of these subjects used
cannabis more than once daily, five (16%) used it daily, eight (25%) used
it weekly and nine (28%) used it rarely. Pain, sleep and mood were most
frequently reported as improving with cannabis use, and 'high' and dry
mouth were the most commonly reported side effects. We conclude that
cannabis use is prevalent among the chronic non-cancer pain population,
for a wide range of symptoms, with considerable variability in the amounts
used. Discussions between patients and health care providers concerning
cannabis use may facilitate education and follow up, and would allow side
effects and potential interactions with other medications to be monitored.
Clinical trials of cannabis for chronic non-cancer pain are warranted.
AD - McGill University Health Center, Pain Center, Montreal General Hospital,
Room D10.137, 1650 Cedar Avenue, Quebec, H3G 1A4, Montreal, Canada
FAU - Ware, Mark A
AU - Ware MA
FAU - Doyle, Crystal R
AU - Doyle CR
FAU - Woods, Ryan
AU - Woods R
FAU - Lynch, Mary E
AU - Lynch ME
FAU - Clark, Alexander J
AU - Clark AJ
LA - eng
PT - Journal Article
CY - Netherlands
TA - Pain
JID - 7508686
SB - IM
EDAT- 2003/03/07 04:00
MHDA- 2003/03/07 04:00
AID - S0304395902004001 [pii]
PST - ppublish
SO - Pain 2003 Mar;102(1-2):211-6.


UI - 22508795
PMID- 12620610
DA - 20030306
IS - 0304-3959
VI - 102
IP - 1-2
DP - 2003 Mar
TI - Changes in intensity, location, and quality of vaso-occlusive pain in
children with sickle cell disease.
PG - 187-93
AB - A descriptive, longitudinal design was used to examine changes in current,
worst, and least pain intensity during hospitalization for a
vaso-occlusive episode in children with sickle cell disease. Other
dimensions of the pain experience including location and quality were also
evaluated. Children reported severe pain on the day of admission with 50%
of the episodes showing a current pain intensity score of >70 and a worst
pain intensity score of >80. Although both pain intensity scores
demonstrated statistically significant decreases by approximately 5% over
the course of the hospitalization, these decreases were not clinically
significant based on the recommendations made in the American Pain
Society's Guideline for the management of acute and chronic pain in sickle
cell disease. In contrast to the pain intensity ratings, which did not
decrease in 25% of the episodes, pain location surface area decreased in
100% of the episodes. Children described the quality of vaso-occlusive
pain using all categories of word descriptors from the adolescent
pediatric pain tool. These findings suggest that pain associated with a
vaso-occlusive episode is inadequately assessed and managed during
hospitalization.
AD - Children's Hospital Oakland, 747, 52nd Street, 94602, Oakland, CA, USA
FAU - Jacob, Eufemia
AU - Jacob E
FAU - Miaskowski, Christine
AU - Miaskowski C
FAU - Savedra, Marilyn
AU - Savedra M
FAU - Beyer, Judith E
AU - Beyer JE
FAU - Treadwell, Marsha
AU - Treadwell M
FAU - Styles, Lori
AU - Styles L
LA - eng
PT - Journal Article
CY - Netherlands
TA - Pain
JID - 7508686
SB - IM
EDAT- 2003/03/07 04:00
MHDA- 2003/03/07 04:00
AID - S0304395902003743 [pii]
PST - ppublish
SO - Pain 2003 Mar;102(1-2):187-93.


UI - 22508793
PMID- 12620608
DA - 20030306
IS - 0304-3959
VI - 102
IP - 1-2
DP - 2003 Mar
TI - Musculoskeletal pain in the Netherlands: prevalences, consequences and
risk groups, the DMC(3)-study.
PG - 167-78
AB - The objective of this paper was to present estimates on the prevalence of
musculoskeletal pain of five different anatomical areas and ten anatomical
sites, and their consequences and risk groups in the general Dutch
population. Cross-sectional data from a population-based study of a
sex-age stratified sample of Dutch inhabitants of 25 years and older were
used. With a postal questionnaire data was assessed on musculoskeletal
pain, additional pain characteristics (location, duration, course), its
consequences (utilization of health care, sick leave and limitation in
daily life) and general socio-demographic characteristics. The top three
of self-reported musculoskeletal pain (point prevalence (P(p)) with 95%
confidence interval (CI)) was: (1) low back pain, P(p)=26.9% (95% CI
25.5-28.3); (2) shoulder pain, P(p)=20.9% (95% CI 19.6-22.2); and (3) neck
pain, P(p)=20.6% (95% CI 19.3-21.9). In most cases the pain was described
as continuous or recurrent and mild. In every three out of ten cases the
complaints about pain were accompanied by limitations in daily living.
Between 33 and 42% of those with complaints consulted their general
practitioner about their pain. With the exception of persons who are work
disabled, general sociodemographic characteristics cannot be used to
identify high risk groups. Musculoskeletal pain is common in all subgroups
of the population and has far-reaching consequences for health, work and
the use of health care.
AD - National Institute of Public Health and the Environment, Center for
Chronic Diseases Epidemiology (CZE, pb 101), PO box 1, 3720 BA, Bilthoven,
The Netherlands
FAU - Picavet, H S J
AU - Picavet HS
FAU - Schouten, J S A G
AU - Schouten JS
LA - eng
PT - Journal Article
CY - Netherlands
TA - Pain
JID - 7508686
SB - IM
EDAT- 2003/03/07 04:00
MHDA- 2003/03/07 04:00
AID - S030439590200372X [pii]
PST - ppublish
SO - Pain 2003 Mar;102(1-2):167-78.


UI - 22508789
PMID- 12620604
DA - 20030306
IS - 0304-3959
VI - 102
IP - 1-2
DP - 2003 Mar
TI - Transgene-mediated enkephalin release enhances the effect of morphine and
evades tolerance to produce a sustained antiallodynic effect in
neuropathic pain.
PG - 135-42
AB - We examined the pharmacologic characteristics of herpes simplex virus
(HSV) vector-mediated expression of proenkephalin in the dorsal root
ganglion in a rodent model of neuropathic pain. We found that: (i)
vector-mediated enkephalin produced an antiallodynic effect that was
reversed by naloxone; (ii) vector-mediated enkephalin production in
animals with spinal nerve ligation prevented the induction of c-fos
expression in second order sensory neurons in the dorsal horn of spinal
cord; (iii) the effect of vector-mediated enkephalin enhanced the effect
of morphine, reducing the ED(50) of morphine 10-fold; (iv) animals did not
develop tolerance to the continued production of vector-mediated
enkephalin over a period of several weeks; and, (v) vector transduction
continued to provide an analgesic effect despite the induction of
tolerance to morphine. This is the first demonstration of gene transfer to
provide an analgesic effect in neuropathic pain. The pharmacologic
analysis demonstrates that transgene-mediated expression and local release
of opioid peptides produce some effects that are distinct from peptide
analogues delivered pharmacologically.
AD - Department of Neurology, University of Pittsburgh, 15213, Pittsburgh, PA,
USA
FAU - Hao, Shuanglin
AU - Hao S
FAU - Mata, Marina
AU - Mata M
FAU - Goins, William
AU - Goins W
FAU - Glorioso, Joseph C
AU - Glorioso JC
FAU - Fink, David J
AU - Fink DJ
LA - eng
PT - Journal Article
CY - Netherlands
TA - Pain
JID - 7508686
SB - IM
EDAT- 2003/03/07 04:00
MHDA- 2003/03/07 04:00
AID - S0304395902003469 [pii]
PST - ppublish
SO - Pain 2003 Mar;102(1-2):135-42.


UI - 22508787
PMID- 12620602
DA - 20030306
IS - 0304-3959
VI - 102
IP - 1-2
DP - 2003 Mar
TI - Self-reports of pain intensity and direct observations of pain behavior:
when are they correlated?
PG - 109-24
AB - Meta-analytic techniques were utilized to investigate the relationship
between self-reports of pain intensity and direct observations of pain
behavior. Estimation of the overall effect size from 29 studies and 85
effect sizes yielded a moderately positive association, z=0.26. High
variability across studies permitted a random-effects moderator analysis
that determined chronicity of pain, the timing of the pain assessment, the
use of global measures of pain behavior, and pain site significantly
moderate the relationship between self-reports of pain intensity and
direct observations of pain behavior. These findings indicate that
self-reports of pain intensity and direct observations of pain behavior
are more likely to be significantly related to each other when the
individual being studied has acute pain (z=0.35), when the self-report of
pain intensity data are collected soon after the observation of pain
behavior (z=0.40), when global composite measures are used to quantify
pain behavior (z=0.37), and when the person being observed suffers from
chronic low back pain (z=0.30). Other factors not found to be significant
moderators include: extent of observer training, relevance of the
pain-inducing task, and pain behavior observation measure used. The
implications of the findings for the assessment of pain are discussed.
AD - Department of Psychology, Ohio University, Athens, OH 45701, USA
FAU - Labus, Jennifer S
AU - Labus JS
FAU - Keefe, Francis J
AU - Keefe FJ
FAU - Jensen, Mark P
AU - Jensen MP
LA - eng
PT - Journal Article
CY - Netherlands
TA - Pain
JID - 7508686
SB - IM
EDAT- 2003/03/07 04:00
MHDA- 2003/03/07 04:00
AID - S0304395902003548 [pii]
PST - ppublish
SO - Pain 2003 Mar;102(1-2):109-24.


UI - 22508786
PMID- 12620601
DA - 20030306
IS - 0304-3959
VI - 102
IP - 1-2
DP - 2003 Mar
TI - Pain and the defense response: structural equation modeling reveals a
coordinated psychophysiological response to increasing painful
stimulation.
PG - 97-108
AB - The defense response theory implies that individuals should respond to
increasing levels of painful stimulation with correlated increases in
affectively mediated psychophysiological responses. This paper employs
structural equation modeling to infer the latent processes responsible for
correlated growth in the pain report, evoked potential amplitudes, pupil
dilation, and skin conductance of 92 normal volunteers who experienced 144
trials of three levels of increasingly painful electrical stimulation. The
analysis assumed a two-level model of latent growth as a function of
stimulus level. The first level of analysis formulated a nonlinear growth
model for each response measure, and allowed intercorrelations among the
parameters of these models across individuals. The second level of
analysis posited latent process factors to account for these
intercorrelations. The best-fitting parsimonious model suggests that two
latent processes account for the correlations. One of these latent
factors, the activation threshold, determines the initial threshold
response, while the other, the response gradient, indicates the magnitude
of the coherent increase in response with stimulus level. Collectively,
these two second-order factors define the defense response, a broad
construct comprising both subjective pain evaluation and physiological
mechanisms.
AD - Pain Research Center, Department of Anesthesiology, University of Utah
School of Medicine, 615 Arapeen Drive, 84108, Salt Lake City, UT, USA
FAU - Donaldson, Gary W
AU - Donaldson GW
FAU - Chapman, C Richard
AU - Chapman CR
FAU - Nakamura, Yoshi
AU - Nakamura Y
FAU - Bradshaw, David H
AU - Bradshaw DH
FAU - Jacobson, Robert C
AU - Jacobson RC
FAU - Chapman, Christopher N
AU - Chapman CN
LA - eng
PT - Journal Article
CY - Netherlands
TA - Pain
JID - 7508686
SB - IM
EDAT- 2003/03/07 04:00
MHDA- 2003/03/07 04:00
AID - S0304395902003512 [pii]
PST - ppublish
SO - Pain 2003 Mar;102(1-2):97-108.


UI - 22508785
PMID- 12620600
DA - 20030306
IS - 0304-3959
VI - 102
IP - 1-2
DP - 2003 Mar
TI - Temporal summation of pain from mechanical stimulation of muscle tissue in
normal controls and subjects with fibromyalgia syndrome.
PG - 87-95
AB - Individuals diagnosed with fibromyalgia syndrome (FMS) report chronic pain
that is frequently worsened by physical activity and improved by rest.
Palpation of muscle and tendinous structures suggests that nociceptors in
deep tissues are abnormally sensitive in FMS, but methods of controlled
mechanical stimulation of muscles are needed to better characterize the
sensitivity of deep tissues. Accordingly, force-controlled mechanical
stimulation was applied to the flexor digitorum muscle of the forearm in a
series of brief contacts (15 stimuli, each of 1s duration, at 3 or 5s
interstimulus intervals). Repetitive stimulation was utilized to determine
whether temporal summation of deep muscular pain would occur for normal
subjects and would be enhanced for FMS subjects. Moderate temporal
summation of deep pain was observed for normal controls (NC), and temporal
summation was greatly exaggerated for FMS subjects. Temporal summation for
FMS subjects occurred at substantially lower forces and at a lower
frequency of stimulation. Furthermore, painful after-sensations were
greater in amplitude and more prolonged for FMS subjects. These
observations complement a previous demonstration that temporal summation
of pain and after-sensations elicited by thermal stimulation of the skin
are moderately enhanced for FMS subjects. Abnormal input from muscle
nociceptors appears to underlie production of central sensitization in FMS
that generalizes to input from cutaneous nociceptors.
AD - Department of Medicine, McKnight Brain Institute, University of Florida
College of Medicine, 1600 SW Archer Rd, P.O. Box 100221, 32610-0221,
Gainesville, FL, USA
FAU - Staud, Roland
AU - Staud R
FAU - Cannon, Richard C
AU - Cannon RC
FAU - Mauderli, Andre P
AU - Mauderli AP
FAU - Robinson, Michael E
AU - Robinson ME
FAU - Price, Donald D
AU - Price DD
FAU - Vierck, Charles J
AU - Vierck CJ
LA - eng
PT - Journal Article
CY - Netherlands
TA - Pain
JID - 7508686
SB - IM
EDAT- 2003/03/07 04:00
MHDA- 2003/03/07 04:00
AID - S0304395902003445 [pii]
PST - ppublish
SO - Pain 2003 Mar;102(1-2):87-95.


UI - 22508782
PMID- 12620597
DA - 20030306
IS - 0304-3959
VI - 102
IP - 1-2
DP - 2003 Mar
TI - Chronic neck pain disability due to an acute whiplash injury.
PG - 63-71
AB - Several theories about musculoskeletal pain syndromes such as
whiplash-associated disorder (WAD) suggest that pain and muscle activity
interact and may contribute to the chronicity of symptoms. Studies using
surface electromyography (sEMG) have demonstrated abnormal muscle
activation patterns of the upper trapezius muscles in the chronic stage of
WAD (grade II). There are, however, no studies that confirm that these
muscle reactions are initiated in the acute stage of WAD, nor that these
muscle reactions persist in the transition from acute neck pain to chronic
neck pain disability.We analyzed the muscle activation patterns of the
upper trapezius muscles in a cohort of 92 subjects with acute neck pain
due to a motor vehicle accident (MVA). This cohort was followed up in
order to evaluate differences in muscular activation patterns between
subjects who have recovered and those subjects who have not recovered
following an acute WAD and developed chronic neck pain. sEMG parameters
were obtained at 1, 4, 8, 12, and 24 weeks after an MVA. The level of
muscle reactivity (the difference in pre- and post-exercise EMG levels)
and the level of muscle activity during an isometric and a dynamic task
were used as EMG parameters.The results revealed no elevated muscle
reactivity either in the acute stage, or during the follow-up period. The
results of both the isometric and dynamic task, showed statistically
significant different EMG levels between four neck pain disability
subgroups (analysis of variance reaching P-levels of 0.000), with an
inverse relationship between the level of neck pain disability and EMG
level. Furthermore, follow-up assessments of the EMG level during these
two tasks, did not show a time related change.In conclusion, in subjects
with future disability, the acute stage is characterized by a
reorganization of the muscular activation of neck and shoulder muscles,
possibly aimed at minimizing the use of painful muscles. This change of
motor control, is in accordance with both the (neurophysiological) 'pain
adaptation model' and (cognitive behavioral) 'fear avoidance model'.
AD - Roessingh, Research and Development, Roessinghsbleekweg 33, 7500 AH,
Enschede, The Netherlands
FAU - Nederhand, Marc J
AU - Nederhand MJ
FAU - Hermens, Hermie J
AU - Hermens HJ
FAU - IJzerman, Maarten J
AU - IJzerman MJ
FAU - Turk, Dennis C
AU - Turk DC
FAU - Zilvold, Gerrit
AU - Zilvold G
LA - eng
PT - Journal Article
CY - Netherlands
TA - Pain
JID - 7508686
SB - IM
EDAT- 2003/03/07 04:00
MHDA- 2003/03/07 04:00
AID - S0304395902003408 [pii]
PST - ppublish
SO - Pain 2003 Mar;102(1-2):63-71.


UI - 22508778
PMID- 12620593
DA - 20030306
IS - 0304-3959
VI - 102
IP - 1-2
DP - 2003 Mar
TI - Anti-allodynic effect of NW-1029, a novel Na(+) channel blocker, in
experimental animal models of inflammatory and neuropathic pain.
PG - 17-25
AB - NW-1029, a benzylamino propanamide derivative, was selected among several
molecules of this chemical class on the basis of its affinity for the
[(3)H]batracotoxin ligand displacement of the Na(+) channel complex and
also on the basis of its voltage and use-dependent inhibitory action on
the Na(+) currents of the rat DRG (dorsal root ganglia) sensory neuron.
This study evaluated the analgesic activity of NW-1029 in animal models of
inflammatory and neuropathic pain (formalin test in mice, complete
Freund's adjuvant and chronic constriction injury in rats) as well as in
acute pain test (hot-plate and tail-flick in rats). Orally administered
NW-1029 dose-dependently reduced cumulative licking time in the early and
late phase of the formalin test (ED(50)=10.1 mg/kg in the late phase). In
the CFA model, NW-1029 reversed mechanical allodynia (von Frey test) after
both i.p. and p.o. administration (ED(50)=0.57 and 0.53 mg/kg),
respectively. Similarly, NW-1029 reversed mechanical allodynia in the CCI
model after both i.p. and p.o. administration yielding an ED(50) of 0.89
and 0.67 mg/kg, respectively. No effects were observed in the hot-plate
and tail-flick tests up to 30 mg/kg p.o. The compound orally administered
(0.1-10 mg/kg) was well tolerated, without signs of neurological
impairment up to high doses (ED(50)=470 and 245 mg/kg in rat and mice
Rotarod test, respectively). These results indicate that NW-1029 has
anti-nociceptive properties in models of inflammatory and neuropathic
pain.
AD - Newron Pharmaceuticals S.p.A Research and Development, Gerenzano, Varese,
Italy
FAU - Veneroni, O
AU - Veneroni O
FAU - Maj, R
AU - Maj R
FAU - Calabresi, M
AU - Calabresi M
FAU - Faravelli, L
AU - Faravelli L
FAU - Fariello, R G
AU - Fariello RG
FAU - Salvati, P
AU - Salvati P
LA - eng
PT - Journal Article
CY - Netherlands
TA - Pain
JID - 7508686
SB - IM
EDAT- 2003/03/07 04:00
MHDA- 2003/03/07 04:00
AID - S0304395902001835 [pii]
PST - ppublish
SO - Pain 2003 Mar;102(1-2):17-25.


UI - 22508776
PMID- 12620591
DA - 20030306
IS - 0304-3959
VI - 102
IP - 1-2
DP - 2003 Mar
TI - Translation of symptoms and signs into mechanisms in neuropathic pain.
PG - 1-8
AD - Department of Neurology, Aarhus University, DK 8000, Aarhus C, Denmark
FAU - Jensen, Troels S
AU - Jensen TS
FAU - Baron, Ralf
AU - Baron R
LA - eng
PT - Journal Article
CY - Netherlands
TA - Pain
JID - 7508686
SB - IM
EDAT- 2003/03/07 04:00
MHDA- 2003/03/07 04:00
AID - S030439590300006X [pii]
PST - ppublish
SO - Pain 2003 Mar;102(1-2):1-8.


UI - 22454883
PMID- 12567037
DA - 20030204
DCOM- 20030304
IS - 1528-1159
VI - 28
IP - 3
DP - 2003 Feb 1
TI - The effectiveness of standard care, early intervention, and occupational
management in worker's compensation claims.
PG - 299-304
AB - STUDY DESIGN: A retrospective and prospective cohort. OBJECTIVES: To
compare the effectiveness of occupational intervention, early
intervention, and standard care in the management of Worker's Compensation
injury claims. SUMMARY OF BACKGROUND DATA: The current management of
occupational back pain and work-related upper extremity disorders with
either standard care or early intervention appears to be ineffective.
METHODS: A retrospective cohort compared injury claim incidence, duration,
and costs between one company with access to standard care and another
similar company with access to early intervention. A prospective cohort
looked at the effect of one company changing from standard care to
occupational management in comparison with the control group with early
intervention. Survival analysis was used to attempt to explain differences
in injury claim duration. RESULTS: Standard care resulted in lower injury
claim incidence, duration, and costs than early intervention, whereas
occupational management resulted in lower injury claim incidence,
duration, and costs than standard care. The covariates of physical
therapist involvement, chiropractor involvement, injury severity, and
relationship between Worker's Compensation and the employer were
associated with delayed time to claim closure in the company with access
to early intervention with the most important covariate being physical
therapist involvement (hazard rate ratio 19.88, 95% confidence interval
7.95-39.77). Only the covariate of injury severity was associated with
delayed time to claim closure in the company with access to occupational
management (hazard rate ratio 1.67, 95% confidence interval 1.05-27.20).
CONCLUSIONS: It is recommended that an occupational management approach,
in comparison with standard care or early intervention, be considered for
management of occupational injuries.
AD - College of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan,
Canada.
FAU - Lemstra, Mark
AU - Lemstra M
FAU - Olszynski, W P
AU - Olszynski WP
LA - eng
PT - Journal Article
CY - United States
TA - Spine
JID - 7610646
SB - IM
MH - Accidents, Occupational/economics/statistics & numerical data
MH - Back Pain/economics/epidemiology/rehabilitation
MH - Cohort Studies
MH - Comorbidity
MH - Disability Evaluation
MH - *Disease Management
MH - Human
MH - Incidence
MH - Industry/statistics & numerical data
MH - Manipulation, Chiropractic/economics/utilization
MH - Occupational Diseases/economics/epidemiology/*rehabilitation
MH - Occupational Health Services/economics/*standards
MH - *Outcome Assessment (Health Care)
MH - Physical Therapy Techniques/economics/utilization
MH - Prospective Studies
MH - Retrospective Studies
MH - Saskatchewan/epidemiology
MH - Survival Analysis
MH - Workers' Compensation/economics/*statistics & numerical data
EDAT- 2003/02/05 04:00
MHDA- 2003/03/05 04:00
AID - 10.1097/01.BRS.0000042249.21349.22 [doi]
PST - ppublish
SO - Spine 2003 Feb 1;28(3):299-304.


UI - 22454866
PMID- 12567020
DA - 20030204
DCOM- 20030304
IS - 1528-1159
VI - 28
IP - 3
DP - 2003 Feb 1
TI - Rehabilitation following first-time lumbar disc surgery: a systematic
review within the framework of the cochrane collaboration.
PG - 209-18
AB - STUDY DESIGN: A systematic review of randomized controlled trials.
BACKGROUND: Although several rehabilitation programs, physical fitness
programs, or protocols regarding instruction for patients to return to
work after lumbar disc surgery have been suggested, little is known about
the efficacy of these treatments, and there are still persistent fears of
causing reinjury, reherniation, or instability. OBJECTIVES: The objective
of this systematic review was to evaluate the effectiveness of active
treatments that are used in the rehabilitation after first-time lumbar
disc surgery. METHODS: The authors searched the MEDLINE, Embase, and
Psyclit databases up to April 2000 and the Cochrane Controlled Trials
Register 2001, issue 3. Both randomized and nonrandomized controlled
trials on any type of active rehabilitation program after first-time disc
surgery were included. Two independent reviewers performed the inclusion
of studies, and two other reviewers independently performed the
methodologic quality assessment. A rating system that consists of four
levels of scientific evidence summarizes the results. RESULTS: Thirteen
studies were included, six of which were of high quality. There is no
strong evidence for the effectiveness for any treatment starting
immediately postsurgery, mainly because of the lack of good quality
studies. For treatments that start 4 to 6 weeks postsurgery, there is
strong evidence (level 1) that intensive exercise programs are more
effective on functional status and faster return to work (short-term
follow-up) as compared to mild exercise programs, and there is strong
evidence (level 1) that on long-term follow-up there is no difference
between intensive exercise programs and mild exercise programs with regard
to overall improvement. For all other primary outcome measures for the
comparison between intensive and mild exercise programs, there is
conflicting evidence (level 3) with regard to long-term follow-up.
Furthermore, there is no strong evidence for the effectiveness of
supervised training as compared to home exercises. There is also no strong
evidence for the effectiveness of multidisciplinary rehabilitation as
compared to usual care. There is limited evidence (level 3) that
treatments in working populations that aim at return to work are more
effective than usual care with regard to return to work. Also, there is
limited evidence (level 3) that low-tech and high-tech exercises, started
more than 12 months postsurgery, are more effective in improving low-back
functional status as compared to physical agents, joint manipulations, or
no treatment. Finally, there is no strong evidence for the effectiveness
of any specific intervention when added to an exercise program, regardless
of whether exercise programs start immediately postsurgery or later. None
of the investigated treatments seem harmful with regard to reherniation or
reoperation. CONCLUSIONS: There is no evidence that patients need to have
their activities restricted after first-time lumbar disc surgery. There is
strong evidence for intensive exercise programs (at least if started about
4-6 weeks postoperative) and no evidence they increase the reoperation
rate. It is unclear what the exact content of postsurgery rehabilitation
should be. Moreover, there are no studies that investigated whether active
rehabilitation programs should start immediately postsurgery or possibly 4
to 6 weeks later.
AD - Department of Epidemiology, Maastricht University, The Netherlands.
r.ostelo.emgo@med.vu.nl
FAU - Ostelo, Raymond W J G
AU - Ostelo RW
FAU - de Vet, Henrica C W
AU - de Vet HC
FAU - Waddell, Gordon
AU - Waddell G
FAU - Kerckhoffs, Maria R
AU - Kerckhoffs MR
FAU - Leffers, Pieter
AU - Leffers P
FAU - van Tulder, Maurits
AU - van Tulder M
LA - eng
PT - Journal Article
PT - Review
PT - Review, Academic
CY - United States
TA - Spine
JID - 7610646
SB - IM
MH - Comparative Study
MH - Controlled Clinical Trials/statistics & numerical data
MH - *Exercise
MH - Exercise Therapy/methods/*statistics & numerical data
MH - Human
MH - Intervertebral Disk Displacement/*rehabilitation/*surgery
MH - Low Back Pain/etiology/prevention & control/rehabilitation
MH - Lumbosacral Region
MH - *Outcome and Process Assessment (Health Care)/statistics & numerical data
MH - Randomized Controlled Trials/statistics & numerical data
RF - 35
EDAT- 2003/02/05 04:00
MHDA- 2003/03/05 04:00
AID - 10.1097/01.BRS.0000042520.62951.28 [doi]
PST - ppublish
SO - Spine 2003 Feb 1;28(3):209-18.