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4RESULTS
There was no significant difference in response for the same parameters among subjects classified as LDL pattern A or B with the exception of significantly greater ( p = 0.01 ) reduction in mean peak particle diameter in pattern A subjects treated with either garlic or placebo .
300
4RESULTS
There was no significant change in LDL subclass distribution .
301
1CONCLUSIONS
This investigation confirms that garlic therapy has no effect on major plasma lipoproteins and further , that it has no impact on HDL subclasses , Lp ( a ) , apolipoprotein B , postprandial triglycerides or LDL subclass distribution .
302
1CONCLUSIONS
Garlic may have a greater effect on LDL particle diameter in LDL pattern A compared with pattern B subjects .
303
1CONCLUSIONS
This difference was not reflected in other plasma lipid measurements .
304
0BACKGROUND
Ileoscopy is the criterion standard for mucosal lesions of terminal ileum but is performed in 5 % of colonoscopy activity , and the need for training is undefined .
305
3OBJECTIVE
To assess the learning curve and skill-keeping line of ileoscopy .
306
2METHODS
Prospective randomized study .
307
2METHODS
Single GI endoscopy unit .
308
2METHODS
Adult outpatients referred for colonoscopy .
309
2METHODS
Patient randomization to ileocolonoscopy by trainees and seniors .
310
2METHODS
Ileoscopy skill was divided into the following : ileocecal valve ( ICV ) intubation ( success rate , time ) and ileal exploration ( length , time ) .
311
2METHODS
Consecutive blocks of 10 procedures were used to calculate the learning curve and the skill-keeping line .
312
2METHODS
Variables considered to influence ICV intubation were the following : endoscopist experience , ICV morphology , patient age , gender , body mass index , diverticular disease , and preceding abdominal/pelvic surgery .
313
4RESULTS
Learning curve showed that competency in ICV intubation ( 80 % success rate ) and ileal exploration ( 16 cm ) was achieved after 50 procedures .
314
4RESULTS
The skill-keeping line showed that ileoscopy was easy ( 97 % success rate ) , fast ( 1 minute ) , and well accepted up to 45 cm of the ileum .
315
4RESULTS
Thin-lipped and volcanic ICV are the most difficult and easiest to intubate , respectively .
316
4RESULTS
Crohn 's disease and adenomas of the proximal edge of ICV were diagnosed in 2.2 % .
317
1CONCLUSIONS
Training in ileoscopy is recommended to achieve competency , and endoscopists should consider practicing ICV intubation to maintain and increase their skill .
318
1CONCLUSIONS
Ileoscopy can be difficult when the ICV is thin lipped or single bulged , and easy when it has a volcanic morphology .
319
3OBJECTIVE
To estimate minimally important differences ( MIDs ) in scores for the modified Rodnan Skin Score ( mRSS ) and Health Assessment Questionnaire-Disability Index ( HAQ-DI ) in a clinical trial on diffuse systemic sclerosis ( SSc ) .
320
2METHODS
134 people participated in a 2-year , double-blind , randomised clinical trial comparing efficacy of low-dose and high-dose D-penicillamine in diffuse SSc .
321
2METHODS
At 6 , 12 , 18 and 24 months , the investigator was asked to rate the change in the patient 's health since entering the study : markedly worsened , moderately worsened , slightly worsened , unchanged , slightly improved , moderately improved or markedly improved .
322
2METHODS
Patients who were rated as slightly improved were defined as the minimally changed subgroup and compared with patients rated as moderately or markedly improved .
323
4RESULTS
The MID estimates for the mRSS improvement ranged from 3.2 to 5.3 ( 0.40-0 .66 effect size ) and for the HAQ-DI from 0.10 to 0.14 ( 0.15-0 .21 effect size ) .
324
4RESULTS
Patients who were rated to improve more than slightly were found to improve by 6.9-14 .2 ( 0.86-1 .77 effect size ) on the mRSS and 0.21-0 .55 ( 0.32-0 .83 effect size ) on the HAQ-DI score .
325
1CONCLUSIONS
MID estimates are provided for improvement in the mRSS and HAQ-DI scores , which can help in interpreting clinical trials on patients with SSc and be used for sample size calculation for future clinical trials on diffuse SSc .
326
3OBJECTIVE
Long-term pharmacological glucocorticoid ( GC ) therapy leads to skeletal muscle atrophy and weakness .
327
3OBJECTIVE
The objective of this study was to investigate whether short-term treatment with GH and testosterone ( T ) can increase lean mass without major impairment of glucose homoeostasis in patients on GC therapy .
328
2METHODS
This was a prospective , open-label , randomised , crossover study .
329
2METHODS
Twelve men ( age 746 years ) on chronic GC treatment participated .
330
2METHODS
The effects of 2 weeks ' treatment with GH , testosterone and the combination of both on lean body mass ( LBM ) , appendicular skeletal muscle mass ( ASMM ) , extracellular water ( ECW ) , body cell mass ( BCM ) and plasma glucose concentrations were investigated .
331
4RESULTS
LBM increased significantly after GH ( 1.71.4 kg ; P = 0.007 ) and GH + testosterone ( 2.41.1 kg ; P = 0.003 ) , but not testosterone alone .
332
4RESULTS
ASMM increased after all three treatment periods ; by 1.00.8 kg after GH ( P = 0.005 ) , 1.70.4 kg after GH + testosterone ( P = 0.002 ) and 0.81.0 kg after testosterone ( P = 0.018 ) .
333
4RESULTS
The increase in ASMM was larger with combined treatment than either GH or testosterone alone ( P < 0.05 ) .
334
4RESULTS
ECW increased significantly after GH + testosterone by 1.52.6 l ( P = 0.038 ) but not after GH or testosterone alone .
335
4RESULTS
BCM increased slightly after single and combined treatments , but the changes were not significant .
336
4RESULTS
Fasting glucose increased significantly after GH ( 0.40.4 mmol/l , P = 0.006 ) while both fasting ( 0.20.3 mmol/l , P = 0.045 ) and post glucose-load ( 1.82.3 mmol/l , P = 0.023 ) plasma glucose concentrations increased after GH + testosterone .
337
1CONCLUSIONS
GH and testosterone induce favourable and additive body compositional changes in men on chronic , low-dose GC treatment .
338
1CONCLUSIONS
In the doses used , combination therapy increases fasting and postprandial glucose concentration .
339
0BACKGROUND
Utilization rates ( URs ) for implantable cardioverter-defibrillators ( ICDs ) for primary prevention of sudden cardiac death ( PPSCD ) are lacking in the community .
340
3OBJECTIVE
The purpose of this study was to establish the ICD UR in central Indiana .
341
2METHODS
A query run on 2 hospitals in a health information exchange database in Indianapolis identified patients between 2011 and 2012 with left ventricular ejection fraction ( EF ) 0.35 .
342
2METHODS
ICD eligibility and utilization were determined from chart review .
343
4RESULTS
We identified 1863 patients with at least 1 low EF study .
344
4RESULTS
Two cohorts were analyzed : 1672 patients without and 191 patients with International Classification of Diseases , Ninth Revision , Clinical Modification procedure code 37.94 for ICD placement .
345
4RESULTS
We manually reviewed a stratified ( by hospital ) random sample of 300 patients from the no-ICD procedure code cohort and found that 48 ( 16 % ) had no ICD but had class I indications for ICD .
346
4RESULTS
Eight of 300 ( 2.7 % ) actually had ICD implantation for PPSCD .
347
4RESULTS
Review of all 191 patients in the ICD procedure code cohort identified 70 with ICD implantation for PPSCD .
348
4RESULTS
The ICD UR ( ratio between patients with ICD for PPSCD and all with indication ) was 38 % overall ( 95 % confidence interval [ CI ] 28 % -49 % ) .
349
4RESULTS
URs were 48 % for males ( 95 % CI 34 % -61 % ) , 21 % for females ( 95 % CI 16 % -26 % , P = .0002 vs males ) , 40 % for whites ( 95 % CI 27 % -53 % ) , and 37 % for blacks ( 95 % CI 28 % -46 % , P = .66 vs whites ) .
350
1CONCLUSIONS
ICD UR is 38 % among patients meeting class I indications , suggesting further opportunities for improving guideline compliance .
351
1CONCLUSIONS
This study also illustrates limitations in calculating ICD UR using large electronic repositories without hands-on chart review .
352
3OBJECTIVE
The study 's purpose was to analyze the effects of exercise training on exercise tolerance and left ventricular systolic function and structure in heart failure patients with preserved , mild , and moderate to severe reduction of left ventricular ejection fraction ( LVEF ) .
353
2METHODS
Ninety-eight patients with moderate to severe ( n = 34 ) , mild ( n = 33 ) , and preserved ( n = 31 ) LVEF were randomly assigned to exercise training plus usual care ( n = 65 ) or usual care alone ( n = 33 ) in a randomization ratio of 2:1 .
354
2METHODS
Left ventricular function , left ventricular dimensions , and exercise tolerance were assessed before and after each intervention .
355
4RESULTS
Exercise tolerance and LVEF increased with exercise training in all patient groups , whereas they remained unchanged after usual care alone .
356
4RESULTS
Exercise training increased the mean ratio of early to late mitral inflow velocities ( E/A ratio ) and decreased deceleration time ( DT ) of early filling in patients with mild and preserved LVEF .
357
4RESULTS
In patients with moderate to severe systolic dysfunction and advanced diastolic dysfunction ( DT < 160 ms ) , exercise training decreased E/A ratio and increased DT , both of which were unchanged after usual care alone .
358
4RESULTS
In the remaining patients ( DT > 160 ms ) , exercise training also improved mitral inflow patterns .
359
4RESULTS
Exercise training decreased left ventricular dimensions in patients with mild and moderate to severe reduction of LVEF but not in patients with preserved LVEF .
360
1CONCLUSIONS
These results indicate that exercise training can improve the course of heart failure independent of the degree of baseline left ventricular dysfunction .
361
3OBJECTIVE
To investigate the feasibility of implementing a Sleep Education Program ( SEP ) for improving sleep in adult family home ( AFH ) residents with dementia , and the relative efficacy of SEP compared with usual care control in a pilot randomized controlled trial .
362
2METHODS
Thirty-seven AFH staff-caregivers and 47 residents with comorbid dementia and sleep disturbances .
363
2METHODS
SEP consisted of four training sessions with staff-caregivers to develop and implement individualized resident behavioral sleep plans .
364
2METHODS
Treatment fidelity to the SEP was assessed following the National Institutes of Health ( NIH ) Behavior Change Consortium model utilizing trainer observations and staff-caregiver reports .
365
2METHODS
Resident sleep was assessed by wrist actigraphy at baseline , 1-month posttreatment , and 6-month follow-up .
366
2METHODS
Caregiver reports of resident daytime sleepiness , depression , and disruptive behaviors were also collected .
367
4RESULTS
Each key area of treatment fidelity ( SEP delivery , receipt , enactment ) was identified , measured , and yielded significant outcomes .
368
4RESULTS
Staff-caregivers learned how to identify sleep scheduling , daily activity , and environmental factors that could contribute to nocturnal disturbances and developed and implemented strategies for modifying these factors .
369
4RESULTS
SEP decreased the frequency and disturbance level of target resident nocturnal behaviors and improved actigraphically measured sleep percent and total sleep time over the 6-month follow-up period compared with the control condition .
370
1CONCLUSIONS
Results suggest behavioral interventions to improve sleep are feasible to implement in adult family homes and merit further investigation as a promising intervention for use with AFH residents with dementia .
371
3OBJECTIVE
To compare the effects of prandial insulin therapy focusing on postprandial glucose control vs. basal insulin therapy focusing on fasting glucose control in patients with type 2 diabetes .
372
2METHODS
This was an open-label , randomized , parallel , three-arm multicenter trial in patients with type 2 diabetes starting insulin treatment .
373
2METHODS
Patients ( n = 159 ) were randomly assigned to 24-week treatment with 3x daily insulin lispro , 3x daily lispro mid mixture ( MidMix ; 50 % lispro , 50 % protaminated lispro ) , or 1x daily insulin glargine ; oral antihyperglycemic agents were discontinued .
374
2METHODS
Primary end point was the postprandial glucose excursion 2 h after breakfast at the end of study .
375
2METHODS
Secondary outcomes included HbA1c , self-monitored blood glucose profiles , hypoglycemic episodes , body weight , and patient satisfaction .
376
4RESULTS
At the end of study , glucose excursions 2 h after breakfast were significantly lower with lispro and MidMix than with glargine ( P < .001 for each vs. glargine ) : lispro , -0.6 + / -2.0 mmol/l ; MidMix , +0.8 + / -2.4 mmol/l ; glargine , +2.5 + / -2.4 mmol/l .
377
4RESULTS
Fasting glucose decreases were significantly greater with glargine ( -2.6 + / -2.4 mmol/l ) than with lispro or MidMix ( -0.9 + / -2.2 mmol/l ; +0.9 + / -1.8 mmol/l ) .
378
4RESULTS
Nevertheless , HbA1c decreased by 1.1 % ( lispro ) and 1.2 % ( MidMix ) , vs. 0.3 % with glargine .
379
4RESULTS
Hypoglycemic episodes were rare with 1-1 .5 self-reported episodes per 100 patient-days .
380
1CONCLUSIONS
In patients with type 2 diabetes starting insulin , 3x daily prandial treatment with a rapid-acting analog focusing on postprandial glucose values enabled better control of postprandial and circadian blood glucose profiles than once-daily glargine , in spite suboptimal fasting glucose levels , which targets fasting glucose values .
381
1CONCLUSIONS
These results support studies suggesting that control of postprandial hyperglycemia plays a key role in achieving HbA1c targets .
382
0BACKGROUND
Female sex workers who inject drugs ( FSW-IDUs ) are at risk of acquiring HIV , sexually transmitted infections ( STI ) and blood-borne infections through unprotected sex and sharing injection equipment .
383
0BACKGROUND
We conducted a 22 factorial randomized controlled trial to evaluate combination interventions to simultaneously reduce sexual and injection risks among FSW-IDUs in Tijuana and Ciudad Juarez , Mexico .
384
2METHODS
FSW-IDUs 18 years reporting sharing injection equipment and unprotected sex with clients within the last month were randomized to one of four conditions based on an a priori randomization schedule , blinding interviewer/counselors to assignment .
385
2METHODS
Due to the extreme vulnerability of this population , we did not include a control group that would deny some women access to preventive information .
386
2METHODS
All women received similar information regardless of group allocation ; the difference was in the way the information was delivered and the extent to which women had an interactive role .
387
2METHODS
Each condition was a single 60-minute session , including either an interactive or didactic version of an injection risk intervention and sexual risk intervention .
388
2METHODS
Women underwent interviewer-administered surveys and testing for HIV , syphilis , gonorrhea , Chlamydia , and Trichomonas at baseline and quarterly for 12 months .
389
2METHODS
Combined HIV/STI incidence will be the primary outcome .
390
2METHODS
Secondary outcomes are proportionate reductions in sharing of injection equipment and unprotected sex with clients .
391
1CONCLUSIONS
Of 1,132 women , 548 ( 48.4 % ) were excluded ( 88.9 % were ineligible ; 11.1 % refused to participate or did not return ) ; 584 eligible women enrolled ( 284 in Tijuana ; 300 in Ciudad Juarez ) .
392
1CONCLUSIONS
All 584 participants completed the baseline interview , provided biological samples and were randomized to one of the four groups .
393
1CONCLUSIONS
During follow-up , 17 participants ( 2.9 % ) were lost to follow-up , of whom 10 ( 58.8 % ) had died , leaving 567 participants for analysis .
394
1CONCLUSIONS
This study appears to be the first intervention to attempt to simultaneously reduce injection and sexual risk behaviors among FSW-IDUs .
395
1CONCLUSIONS
The factorial design will permit analysis to determine whether the combination of the two interactive interventions and/or its respective components are effective in reducing injection and/or sexual risks , which will have direct , tangible policy implications for Mexico and potentially other resource-poor countries .
396
0BACKGROUND
NCT00840658 .
397
3OBJECTIVE
To compare oral risperidone and intramuscular ( IM ) haloperidol , both in combination with IM lorazepam , in the management of acute agitation and psychosis in the medical emergency department .
398
2METHODS
In this prospective , randomized , placebo-controlled , double-blind study of 30 patients presenting to the emergency department with acute agitation and/or psychosis , three groups of 10 patients received oral and IM medications : 1 ) 2 mg oral risperidone and 2 mg IM lorazepam ; 2 ) 5 mg oral haloperidol and 2 mg IM lorazepam ; 3 ) oral placebo and 2 mg IM lorazepam .
399