コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ptive field was in the intact muscles of the low back.
4 ered were: classic SMS (n = 5, involving the low back and lower extremities), variant SMS (n = 2, lim
6 utcome measures included lifetime history of low back and neck pain (using a range of increasingly st
7 llion (UI, $82.7 billion-$92.9 billion), and low back and neck pain accounted for the third-highest a
8 ing on diabetes, ischemic heart disease, and low back and neck pain accounting for the highest amount
12 current US national prevalence estimates of low back and neck pain exist and few studies have invest
14 aemic heart disease, chronic kidney disease, low back and neck pain, and depressive disorders; the la
16 s have investigated the associations between low back and neck pain, psychological factors, and healt
18 of a multidimensional approach to examining low back and neck problems and suggests the need for fur
20 se capacity (-2.0 +/- 2.1 ml/kg per minute), low-back and hamstring flexibility (-4.7 +/- 1.6 cm), an
30 rmacologic management of acute pain from non-low back, musculoskeletal injuries in adults in the outp
31 rmacologic management of acute pain from non-low back, musculoskeletal injuries in adults in the outp
32 s treating patients with acute pain from non-low back, musculoskeletal injuries with opioids, includi
33 ians treat patients with acute pain from non-low back, musculoskeletal injuries with oral NSAIDs to r
34 ians treat patients with acute pain from non-low back, musculoskeletal injuries with specific acupres
35 ians treat patients with acute pain from non-low back, musculoskeletal injuries with topical nonstero
43 The PP group had a significant reduction of low back pain (66.2% vs 50.0%; P = 0.04) and analgesic c
44 am (SMP) on primary care patients with acute low back pain (ALBP) from low income, inner city neighbo
46 2.4 +/- 13 years old; 13F, 12M) with chronic low back pain (cLBP) and 27 healthy control subjects (48
47 stigated thalamocortical networks in chronic low back pain (cLBP) given its non-specific etiology and
49 neural activity in individuals with chronic low back pain (cLBP) remains scarce and results are inco
50 ga is effective for mild to moderate chronic low back pain (cLBP), but its comparative effectiveness
52 the afternoon in 47 subjects without current low back pain (IVDs = 230; age range, 20-71 years) after
53 eloped to screen for risk factors for future low back pain (LBP) -related disability and work loss re
54 ebral disc (IVD) degeneration and consequent low back pain (LBP) are common and costly pathological p
55 d cost-effective primary care treatments for low back pain (LBP) are required to reduce the burden of
65 our of the paraspinal muscles in people with low back pain (LBP); but so far, HDEMG has not been used
66 nal treatments for participants with chronic low back pain (Mint study) were conducted in 16 multidis
67 s that could be confused for musculoskeletal low back pain (nepholithiasis, urinary tract infection,
68 asone recipients demonstrated improvement in low back pain (P = .04, Fisher exact test), whereas 55%
69 betamethasone recipients had improvement in low back pain (P = .26), whereas 49% of triamcinolone re
70 betamethasone recipients had improvement in low back pain (P = .38), whereas 52% of triamcinolone re
73 iagnostic tests in patients with nonspecific low back pain (strong recommendation, moderate-quality e
74 the preceding therapies for acute or chronic low back pain (with or without leg pain) that reported p
78 verity were divided according to symptoms of low back pain alone and symptoms of low back pain with o
80 s a major pathological process implicated in low back pain and is a prerequisite to disk herniation.
81 lly significant difference in improvement in low back pain and lower extremity pain between groups.
82 with betamethasone and triamcinolone reduced low back pain and lower extremity pain, although there w
85 anxiety, musculoskeletal disorders including low back pain and neck pain, diabetes, and cirrhosis--in
86 A 20-year-old man presented with 1 week of low back pain and progressive lower extremity weakness.
87 ic images, intracranial pressure processing, low back pain and real-time tumour tracking; (3) outcome
88 in intensity and disability in patients with low back pain and sciatica after lumbar disc herniation.
89 nce (MR) imaging in patients with persistent low back pain and sciatica effectively demonstrates spin
90 ans should evaluate patients with persistent low back pain and signs or symptoms of radiculopathy or
91 on (SOE, moderate) are effective for chronic low back pain and strengthens previous findings regardin
92 the most important factor leading to chronic low back pain and subsequent disability after discectomy
93 s important to remember about rare causes of low back pain and to perform detailed physical examinati
94 lation (10 kHz SCS) in subjects with chronic low back pain and/or leg pain and performed post hoc ana
98 harmacologic therapies for primarily chronic low back pain are associated with small to moderate, usu
99 of moderate efficacy for chronic or subacute low back pain are cognitive-behavioral therapy, exercise
100 ood evidence of short-term effectiveness for low back pain are NSAIDs, acetaminophen, skeletal muscle
102 ent state of managing chronic (and subacute) low back pain as reflected in recently published guideli
103 ders (1.71 billion people [1.68-1.80]), with low back pain being the most prevalent condition in 134
105 clinically important improvement in chronic low back pain compared with a standardized exercise prog
107 342 adults aged 20 to 70 years with chronic low back pain enrolled between September 2012 and April
108 s approximately 1.5), and a history of prior low back pain episodes and demographic variables were no
109 lated for prediction of persistent disabling low back pain for findings attainable during the clinica
110 thritis (OA), rheumatoid arthritis (RA), and low back pain from 12 community pharmacy sites responded
112 udies of patients with fewer than 8 weeks of low back pain from which likelihood ratios (LRs) were ca
113 en that most patients with acute or subacute low back pain improve over time regardless of treatment,
117 Higher BMI was significantly associated with low back pain in males (for overweight, odds ratio = 1.0
122 carpal tunnel syndrome, 59 million have had low back pain in the past 3 months, and 30.1 million hav
123 ith DZ twins, equating to a heritability for low back pain in the range of 52-68% and for neck pain i
125 ical examination to help place patients with low back pain into 1 of 3 broad categories: nonspecific
135 program to adults with chronic or recurrent low back pain led to greater improvements in back functi
140 ostic imaging is indicated for patients with low back pain only if they have severe progressive neuro
142 clinical trials of participants with chronic low back pain originating in the facet joints, sacroilia
145 Genome-wide-association studies in chronic low back pain patients identified sepiapterin reductase
147 egeneration (IVDD) as major cause of chronic low back pain represent the most common degenerative joi
148 ated to a person's health status) indicating low back pain severity were divided according to symptom
149 atory drugs had smaller benefits for chronic low back pain than previously observed, duloxetine was e
150 endorse triage to identify the rare cases of low back pain that are caused by medically serious patho
151 ive inception cohorts of patients with acute low back pain that measured fear of pain (often describe
152 e preceding medications for acute or chronic low back pain that reported pain outcomes, back-specific
153 The proportion of visits to specialists for low back pain that were new consultations increased from
154 studies varied from a low of 31% (n = 8) for low back pain to a high of 68% (n = 23) for fibromyalgia
155 ic reviews and RCTs, for RCTs of adults with low back pain treated in ambulatory settings with SMT co
156 ard deviation]; age range, 20-79 years) with low back pain underwent standard 1.5-T MR imaging, which
158 ment-evoked pain in individuals with chronic low back pain was associated with longer reaction times,
160 raphy by a sports medicine clinic because of low back pain were evaluated for the presence of asympto
161 mponents for predicting persistent disabling low back pain were maladaptive pain coping behaviors, no
162 nostic imaging and testing for patients with low back pain when severe or progressive neurologic defi
163 Recommendation 3: In patients with chronic low back pain who have had an inadequate response to non
164 y with SPECT can help identify patients with low back pain who would benefit from facet joint injecti
165 ptoms of low back pain alone and symptoms of low back pain with objective corroborating findings.
167 patients with evidence-based information on low back pain with regard to their expected course, advi
168 eporting (OP-8) reduced MR imaging rates for low back pain without conservative therapy in either Med
169 ion of MR imaging examinations performed for low back pain without history of conservative therapy.
170 ed by local DRG inflammation (a rat model of low back pain) and by a peripheral paw inflammation mode
171 h as imaging for patients with uncomplicated low back pain) and using the results for public reportin
173 eas, including several (such as headache and low back pain) commonly encountered by internal medicine
174 nophen, skeletal muscle relaxants (for acute low back pain), and tricyclic antidepressants (for chron
175 nophen, skeletal muscle relaxants (for acute low back pain), and tricyclic antidepressants (for chron
179 2013, and October 24, 2014, and had chronic low back pain, a positive diagnostic block at the facet
180 that acupuncture may be useful for headache, low back pain, alcohol dependence, and paralysis resulti
181 pain and disability in patients with chronic low back pain, although this difference became nonsignif
183 served, duloxetine was effective for chronic low back pain, and benzodiazepines were ineffective for
184 that acetaminophen is ineffective for acute low back pain, and duloxetine is associated with modest
185 for improving function and reducing chronic low back pain, and the benefits persisted for at least s
186 ronic pain, encompassing conditions, such as low back pain, arthritis, persistent post-surgical pain,
187 ack disorders, with a particular emphasis on low back pain, as this area has been most represented in
188 in into 1 of 3 broad categories: nonspecific low back pain, back pain potentially associated with rad
189 sis and assessment of disease progression in low back pain, brain tumours and primary epilepsy; (2) e
190 and height are linked to the pathogenesis of low back pain, but evidence-based confirmation is lackin
191 ion is a commonly used treatment for chronic low back pain, but high-quality evidence for its effecti
192 iscs has been linked with the development of low back pain, but little is known about factors affecti
193 Recommendation 2: For patients with chronic low back pain, clinicians and patients should initially
197 aluated included reduction or elimination of low back pain, improvement in back-specific and overall
198 spinal manipulation; for chronic or subacute low back pain, intensive interdisciplinary rehabilitatio
199 llitus, and chronic pain conditions (chronic low back pain, knee osteoarthritis, and fibromyalgia).
200 with the largest number of YLDs in 2010 were low back pain, major depressive disorder, other musculos
201 that acetaminophen was ineffective for acute low back pain, nonsteroidal anti-inflammatory drugs had
202 heumatoid arthritis, osteoarthritis, chronic low back pain, or ischemic heart disease since 1995.
203 logic therapy with proven benefits-for acute low back pain, spinal manipulation; for chronic or subac
205 fferent rheumatic conditions (eg, neck pain, low back pain, systemic lupus erythematosus, fibromyalgi
210 include intense vulvar and vaginal itching, low back pain, uterine cramps, fetal distress, and prete
211 ne does not address noninvasive treatment of low back pain, which is covered by a separate ACP guidel
212 ty-seven patients (23 men and 24 women) with low back pain, who were scheduled for facet joint inject
213 ive-month period because of an acute, severe low back pain, with sphincter dysfunction, partially res
214 cians and American Pain Society guideline on low back pain, would provide better care to patients, im
273 prevalence of back and/or neck pain was 31% (low back pain: 34 million, neck pain: 9 million, both ba
274 rm trials showing modest effects for chronic low back pain; trials were not designed to assess seriou
276 ity were half as likely to have work-related low-back pain (OR=0.50, 95% CI 0.26-0.96) and nurses rep
277 e-sacral articulation of young patients with low-back pain and a lumbosacral transitional vertebra.
278 e; age range, 6-19 y; mean age, 15.7 y) with low-back pain and a lumbosacral transitional vertebra.
279 maging on clinical outcomes in patients with low-back pain and no indication of serious underlying co
280 r imaging in patients with acute or subacute low-back pain and without features suggesting a serious
282 d effect on troublesome subacute and chronic low-back pain at a low cost to the health-care provider.
283 f different imaging methods, and duration of low-back pain did not affect the results, but analyses w
287 lso observed in a separate cohort of chronic low-back pain patients and was associated with dynamic c
288 rent sites and accurately classified chronic low-back pain patients in two additional independent dat
289 s reproducible across two cohorts of chronic low-back pain patients obtained from different sites and
290 adults with troublesome subacute or chronic low-back pain were recruited from 56 general practices a
292 egenerative disc disease often causes severe low-back pain, a public health problem with huge economi
295 aration of small molecules and proteins with low back pressure are demonstrated by high-performance l
296 ous properties of the monoliths lead to very low back pressures enabling the use of simple mechanical
297 Given their high efficiencies and relatively low back pressures, columns containing these particles w
300 ty after nervous system injuries and painful low back spasm affect more than 10% of global population