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1.
OBJECTIVES: In earlier studies the lack of correlation between subjective need for rehabilitation of the applicant and the medically determined objective need for rehabilitation was reported again and again. The correlation between fatigue and subjective need for rehabilitation was not yet examined so far. Nevertheless fatigue is not defined sufficiently in the ICD, so interactions between chronic fatigue and somatic diseases are not taken into account appropriately. The following questions are considered: How high is the degree of chronic fatigue in insurees applying for rehabilitation? Is there a correlation between degree of fatigue and need for rehabilitation? Is it possible to predict approval of medical rehabilitation by fatigue and need for rehabilitation? How will insurees accept a screening accompanying their application for rehabilitation? METHOD: The study is based on data of 500 (response rate 85.6%) insurees of the pension insurance Braunschweig-Hannover, who had applied for medical rehabilitation between 1/2004 and 3/2004. The screening instrument included: scales on functional activity, mobility, social support, coping (IRES), the Chalder Fatigue Scale, SCL 14, Items concerning need for rehabilitation. As statistical methods t-, chi (2)-test, correlations, covariance-analysis and regression analysis are used. RESULTS: 70.2% of the patients claiming rehabilitation reported relevant clinical symptoms of chronic fatigue. There were no differences in age, work status, motivation, or expectations of returning to work, but differences in sex. Patients with chronic fatigue met more citeria of need for rehabilitation. But the approval of medical rehabilitation could not be predicted by fatigue and need for rehabilitation. Nevertheless the acceptance of the screening was high in the insurees. CONCLUSIONS: Patients with chronic fatigue met more criteria of need for rehabilitation. But the approval of medical rehabilitation could not be predicted by fatigue and need for rehabilitation. We assume that the reduction of activity and participation is associated with the degree of fatigue. It is discussed that the information an investigator may derive from a screening which is accepted by the insurees claiming medical rehabilitation will complete the collected clinical documents in a meaningful manner.  相似文献   

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The widespread use of antibiotics has resulted in a growing problem of antimicrobial resistance in the community and hospital settings. Antimicrobial classes for which resistance has become a major problem include the β-lactams, the glycopeptides, and the fluoroquinolones. In gram-positive bacteria, β-lactam resistance most commonly results from expression of intrinsic low-affinity penicillin-binding proteins. In gram-negative bacteria, expression of acquired β-lactamases presents a particular challenge owing to some natural spectra that include virtually all β-lactam classes. Glycopeptide resistance has been largely restricted to nosocomial Enterococcus faecium strains, the spread of which is promoted by ineffective infection control mechanisms for fecal organisms and the widespread use of colonization-promoting antimicrobials (especially cephalosporins and antianaerobic antibiotics). Fluoroquinolone resistance in community-associated strains of Escherichia coli, many of which also express β-lactamases that confer cephalosporin resistance, is increasingly prevalent. Economic and regulatory forces have served to discourage large pharmaceutical companies from developing new antibiotics, suggesting that the antibiotics currently on the market may be all that will be available for the coming decade. As such, it is critical that we devise, test, and implement antimicrobial stewardship strategies that are effective at constraining and, ideally, reducing resistance in human pathogenic bacteria.  相似文献   

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Abstract

Purpose: The aim of this study was to examine what factors affect the acceptance behavior and use of new technologies for rehabilitation by therapists at a large rehabilitation hospital in Canada. Method: A self-administrated paper-based survey was created by adapting scales with high levels of internal consistency in prior research using the Unified Theory of Acceptance and Use of Technology (UTAUT). Items were scored on a 7-point Likert scale, ranging from “strongly disagree (1)” to “strongly agree (7)”. The target population was all occupational therapists (OT) and physical therapists (PT) involved with the provision of therapeutic interventions at the hospital. Our research model was tested using partial least squares (PLS) technique. Results: Performance expectancy was the strongest salient construct for behavioral intention to use new technologies in rehabilitation, whereas neither effort expectancy nor social influence were salient constructs for behavioral intention to use new technologies; (4) facilitating condition and behavioral intention to use new technologies were salient constructs for current use of new technologies in rehabilitation, with facilitating condition the strongest salient for current use of new technologies in rehabilitation. Conclusion: In a large rehabilitation hospital where use of new technologies in rehabilitation is not mandatory, performance expectancy, or how the technology can help in therapists’ work, was the most important factor in determining therapists’ acceptance and use of technologies. However, effort expectancy and social influence constructs were not important, i.e. therapists were not influenced by the degree of difficulty or social pressures to use technologies. Behavioral intention and facilitating condition, or institutional support, are related to current use of new technologies in rehabilitation.
  • Implications for Rehabilitation
  • Rehabilitation professionals who are faced with using new technologies are less concerned about effort and social pressures, than they are about what the technologies can do for them or their clients.

  • When it comes to new rehabilitation technologies, actual users express intention.

  • Rehabilitation professionals’ acceptance and adoption of technologies rely on conditions that facilitate their use. These conditions include scheduling, support and a conductive environment.

  相似文献   

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8.
Pediatric headache is a common health problem in children, with a significant headache reported in more than 75% by the age of 15 years. Pediatric migraine occurs in up to 10.6% of children between the ages of 5 and 15 years and in up to 28% of adolescents between the ages of 15 and 19 years. Given this high frequency, the impact of this disease on the lives of these children and their parents can be quite significant. This impact can be assessed with disease-specific disability and impairment as well as disease non-specific effects on quality of life. The goal of evaluation should be recognition of this impact, whereas the goal of management should be effective treatment that minimizes the impact of this disorder in the short term and for the life of the patient.  相似文献   

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Class D β-lactamase-mediated resistance to β-lactams has been increasingly reported during the last decade. Those enzymes also known as oxacillinases or OXAs are widely distributed among Gram negatives. Genes encoding class D β-lactamases are known to be intrinsic in many Gram-negative rods, including Acinetobacter baumannii and Pseudomonas aeruginosa, but play a minor role in natural resistance phenotypes. The OXAs (ca. 150 variants reported so far) are characterized by an important genetic diversity and a great heterogeneity in terms of β-lactam hydrolysis spectrum. The acquired OXAs possess either a narrow spectrum or an expanded spectrum of hydrolysis, including carbapenems in several instances. Acquired class D β-lactamase genes are mostly associated to class 1 integron or to insertion sequences.Class D β-lactamases, also known as oxacillinases or OXA-type β-lactamases (OXAs), are active-serine-site enzymes like Ambler class A and class C β-lactamases, differing from class A and C enzymes in amino acid structure, whereas class B β-lactamases are metalloenzymes with a Zn2+ ion(s) in the active site (4, 71, 78). Even though class D includes mostly enzymes with higher hydrolysis rates for cloxacillin and oxacillin than for benzylpenicillin (hence the name oxacillinases), not all class D β-lactamases have this characteristic. Most of the class D enzymes belong to group 2d of the Bush functional classification scheme for β-lactamases (23). Among the four β-lactamase molecular classes, class D β-lactamases are the most diverse enzymes (107). This diversity is observed at both the genetic and biochemical levels, with enzymes possessing either a narrow or expanded spectrum of hydrolysis. In addition, several class D β-lactamases have an expanded spectrum of activity resulting from point mutations.Although many class D β-lactamase genes are embedded into class 1 integrons, recent reports indicated that other specific genetic structures, including insertion sequences and transposons, may be associated with class D β-lactamase genes. Numerous class D β-lactamase genes have been identified as a source of acquired resistance in gram-negative bacteria, but recent studies have shown that class D β-lactamases are also naturally produced in clinically significant pathogens and environmental species (107).This review focuses on the diversity and substrate profiles of class D β-lactamases, their sources, and the genetics of acquisition of the corresponding genes. All the class D β-lactamases for which a sequence is available in the GenBank databases are listed in Table Table11.

TABLE 1.

Features of oxacillinases
NameaAlternate nameOXA groupTypeOriginal hostA or NbAssociated mobile element
Gene GC content (%)Isoelectric pointd
GenBank accession no.eReferencef
Transposon or insertion sequenceIntegroncExptlTheoretical
OXA-1OXA-30Narrow spectrumE. coliATn2603+34.47.47.7J02967113
OXA-2OXA-2Narrow spectrumS. TyphimuriumA+507.79.1X0726097
OXA-3OXA-2Narrow spectrumK. pneumoniaeATn1411+507.18.1L07945142
OXA-4OXA-35Narrow spectrumE. coliATn1409+7.5AY162283142
OXA-5Narrow spectrumP. aeruginosaATn1406+40.27.68.4X5827232
OXA-6Narrow spectrumP. aeruginosaA7.7UP
OXA-7OXA-10Narrow spectrumE. coliA+40.67.79.3X75562145
OXA-8
OXA-9Narrow spectrumK. pneumoniaeATn1331+49.56.97.1M55547155
LCR-1Narrow spectrumP. aeruginosaATn1412526.57.1X5680932
OXA-10Narrow spectrumP. aeruginosaATn1404+42.16.17.0U3710570
OXA-11OXA-10ES-OXAP. aeruginosaA+426.46.3Z2259060
OXA-12Narrow spectrumA. jandaeiN62.38.68.4U10251139
AmpSNarrow spectrumA. hydrophilaN637.97.1X80276165
OXA-13OXA-10Narrow spectrumP. aeruginosaA+41.28.08.7U5918399
OXA-14OXA-10ES-OXAP. aeruginosaA+42.16.26.3L3852338
OXA-15OXA-2ES-OXAP. aeruginosaA+508.79.3U6383536
OXA-16OXA-10ES-OXAP. aeruginosaA+42.16.26.3AF04310039
OXA-17OXA-10ES-OXAP. aeruginosaA+42.16.17.0AF06020637
OXA-18ES-OXAP. aeruginosaAISCR1961.25.55.9U85514118
OXA-19OXA-13ES-OXAP. aeruginosaA+41.27.68.4AF04338198
OXA-20Narrow spectrumP. aeruginosaA+45.17.49.0AF024602108
OXA-21OXA-3Narrow spectrumA. baumanniiA+50.17.08.1Y10693162
OXA-22Narrow spectrumR. pickettiiN65.57.06.4AF064820112
OXA-23CHDLA. baumanniiATn2006/Tn2007386.77.0AJ13210542
OXA-24OXA-40CHDLA. baumanniiA34.48.69.0AJ23912919
OXA-25OXA-40CHDLA. baumanniiA34.48.08.5AF2018261
OXA-26OXA-40CHDLA. baumanniiA34.47.99.0AF2018271
OXA-27OXA-23CHDLA. baumanniiA386.88.0AF2018281
OXA-28OXA-13ES-OXAP. aeruginosaA+41.28.18.7AF231133125
OXA-29Narrow spectrumL. gormaniiN36.69.09.4AJ40061949
OXA-30OXA-1Narrow spectrumE. coliA+34.47.36.8AF255921148
OXA-31OXA-1ES-OXAP. aeruginosaA+34.47.56.8AF2946539
OXA-32OXA-2ES-OXAP. aeruginosaA+507.79.0AF315351124
OXA-33OXA-40CHDLA. baumanniiA34.48.69.0AY008291
OXA-34OXA-2ES-OXAP. aeruginosaA+508.9AF350424UP
OXA-35OXA-10ES-OXAP. aeruginosaA+41.28.08.7AF3157868
OXA-36OXA-2ES-OXAP. aeruginosaA+49.49.2AF300985UP
OXA-37OXA-20Narrow spectrumA. baumanniiA+44.87.48.9AY007784109
OXA-38
OXA-39
OXA-40CHDLA. baumanniiA34.48.69.0AF50924165
OXA-41
OXA-42Narrow spectrumB. pseudomalleiN66.39.29.3AJ488302111
OXA-43Narrow spectrumB. pseudomalleiN65.99.29.3AJ488303111
OXA-44
OXA-45ES-OXAP. aeruginosaAISCR561.88.89.4AJ519683153
OXA-46Narrow spectrumP. aeruginosaA+47.17.88.7AF31751157
OXA-47OXA-1Narrow spectrumK. pneumoniaeA+34.17.46.8AY237830127
OXA-48CHDLK. pneumoniaeATn199944.57.28.0AY236073127
OXA-49OXA-23CHDLA. baumanniiA386.0AY288523UP
OXA-50Narrow spectrumP. aeruginosaN64.88.69.0AY30613054
OXA-51OXA-Ab1CHDLA. baumanniiA39.37.08.0AJ30973422
OXA-52
OXA-53OXA-2ES-OXAS. AgonaA+50.26.97.2AY289608103
OXA-54CHDLS. oneidensisN46.66.86.7AY500137126
OXA-55CHDLS. algaeN53.88.68.6AY34349368
OXA-56Narrow spectrumP. aeruginosaA+40.76.58.7AY44508025
OXA-57Narrow spectrumB. pseudomalleiN669.3AJ63196673
OXA-58CHDLA. baumanniiA37.47.27.2AY665723130
OXA-59Narrow spectrumB. pseudomalleiN65.99.3AJ63224973
OXA-60Narrow spectrumR. pickettiiN64.95.15.4AF52530355
OXA-61Narrow spectrumC. jejuniN27.49.1AY5879562
OXA-62CHDLP. pnomenusaN65.3>9.09.5AY423074144
OXA-63Narrow spectrumB. pilosicoliN24.96.0AY61900394
OXA-64OXA-Ab2OXA-51CHDLA. baumanniiN39.68.0AY75090721
OXA-65OXA-Ab3OXA-51CHDLA. baumanniiN39.28.8AY75090821
OXA-66OXA-Ab4OXA-51CHDLA. baumanniiN39.49.0AY75090921
OXA-67OXA-Ab5OXA-51CHDLA. baumanniiN398.0DQ491200UP
OXA-68OXA-Ab6OXA-51CHDLA. baumanniiN397.1AY75091021
OXA-69OXA-Ab7OXA-51CHDLA. baumanniiN39.38.48.6AY75091166
OXA-70OXA-Ab8OXA-51CHDLA. baumanniiN39.39.0AY75091221
OXA-71OXA-Ab9OXA-51CHDLA. baumanniiN39.78.0AY75091321
OXA-72OXA-40CHDLA. baumanniiA36.48.8EF534256166
OXA-73OXA-23CHDLK. pneumoniaeA37.68.0AY762325UP
OXA-74OXA-10UnknownP. aeruginosaA41.96.57.0AJ85418246
OXA-75OXA-Ab10OXA-51CHDLA. baumanniiN38.78.6AY85952966
OXA-76OXA-Ab11OXA-51CHDLA. baumanniiN39.39.2AY94920366
OXA-77OXA-Ab12OXA-51CHDLA. baumanniiN39.28.6AY94920266
OXA-78OXA-Ab13OXA-51CHDLA. baumanniiN39.28.9AY862132UP
OXA-79OXA-Ab14OXA-51CHDLA. baumanniiN39.59.0EU01953447
OXA-80OXA-Ab15OXA-51CHDLA. baumanniiN39.39.0EU01953547
OXA-81
OXA-82OXA-Ab16OXA-51CHDLA. baumanniiN39.49.0EU019536158
OXA-83OXA-Ab17OXA-51CHDLA. baumanniiN39.59.0DQ309277158
OXA-84OXA-Ab18OXA-51CHDLA. baumanniiN39.49.0DQ309276158
OXA-85Narrow spectrumF. nucleatumN24.65.36.1AY227054164
OXA-86OXA-Ab19OXA-51CHDLA. baumanniiN38.88.0DQ149247159
OXA-87OXA-Ab20OXA-51CHDLA. baumanniiN38.98.0DQ348075159
OXA-88OXA-Ab21OXA-51CHDLA. baumanniiN39.29.2DQ39296375
OXA-89OXA-Ab22OXA-51CHDLA. baumanniiN38.47.08.6DQ44568394
OXA-90OXA-Ab23OXA-51CHDLA. baumanniiN39.28.6EU433382UP
OXA-91OXA-Ab24OXA-51CHDLA. baumanniiN398.0DQ51908375
OXA-92OXA-Ab25OXA-51CHDLA. baumanniiN39.38.6DQ335566156
OXA-93OXA-Ab26OXA-51CHDLA. baumanniiN39.38.0DQ51908775
OXA-94OXA-Ab27OXA-51CHDLA. baumanniiN39.38.9DQ51908875
OXA-95OXA-Ab28OXA-51CHDLA. baumanniiN39.58.6DQ51908975
OXA-96OXA-58CHDLA. baumanniiA37.57.2DQ51909075
OXA-97OXA-58CHDLA. baumanniiA37.87.2EF102240129
OXA-98OXA-Ab29OXA-51CHDLA. baumanniiN39.28.6AM279652UP
OXA-99OXA-Ab30OXA-51CHDLA. baumanniiN39.48.0DQ888718UP
OXA-100
OXA-101OXA-10UnknownC. freundiiA+40.78.8AM412777UP
OXA-102OXA-23CHDLA. radioresistensN385.8Unknown123
OXA-103OXA-23CHDLA. radioresistensN385.8Unknown123
OXA-104OXA-Ab31OXA-51CHDLA. baumanniiN39.38.6EF58128547
OXA-105OXA-23CHDLA. radioresistensN387.0UnknownUP
OXA-106OXA-Ab32OXA-51CHDLA. baumanniiN39.38.9EF65003247
OXA-107OXA-Ab33OXA-51CHDLA. baumanniiN39.38.6EF65003347
OXA-108OXA-Ab34OXA-51CHDLA. baumanniiN398.5EF65003447
OXA-109OXA-Ab35OXA-51CHDLA. baumanniiN39.39.0EF65003547
OXA-110OXA-Ab36OXA-51CHDLA. baumanniiN39.38.6EF65003647
OXA-111OXA-Ab37OXA-51CHDLA. baumanniiN39.47.1EF65003747
OXA-112OXA-Ab38OXA-51CHDLA. baumanniiN39.48.6EF65003847
OXA-113OXA-Ab39OXA-51CHDLA. baumanniiN39.38.0EF653400106
OXA-114Narrow spectrumA. xylosoxidansN70.48.69.0EU18884241
OXA-115OXA-Ab40OXA-51CHDLA. baumanniiN39.39.0EU029998UP
OXA-116OXA-Ab41OXA-51A. baumanniiN39.38.6EU220744UP
OXA-117OXA-Ab42OXA-51A. baumanniiN39.28.6EU220745UP
OXA-118Narrow spectrumB. cepaciaA+49.37.3AF37196433
OXA-119Narrow spectrumUncultured bacteriumA+49.46.7AY139598150
OXA-120
OXA-121
OXA-122
OXA-123
OXA-124
OXA-125
OXA-126
OXA-127
OXA-128OXA-10CHDLA. baumanniiN+39.18.0EU37551552a
OXA-129OXA-Ab43OXA-5UnknownS. BredeneyA+39.99.1AM93266995
OXA-130OXA-Ab44OXA-51A. baumanniiN39.18.5EU547445UP
OXA-131OXA-Ab45OXA-51A. baumanniiN39.49.0EU547446UP
OXA-132OXA-Ab46OXA-51A. baumanniiN39.38.0EU547447UP
OXA-133OXA-23CHDLA. radioresistensN39.36.1EU571228123
OXA-134CHDLA. lwoffiiN46.25.3UP
OXA-135
OXA-136OXA-63Narrow spectrumB. pilosicoliN25.15.3EU08683096
OXA-137OXA-63Narrow spectrumB. pilosicoliN24.95.7EU08683496
OXA-138
OXA-139
OXA-140
OXA-141OXA-2ES-OXAP. aeruginosaA+49.99.1EF552405UP
OXA-142OXA-10ES-OXAP. aeruginosaA+426.3EU358785UP
OXA-143CHDLA. baumanniiA34.48.7UP
OXA-144
OXA-145OXA-10ES-OXAP. aeruginosaA+41.18.7FJ790516UP
OXA-146
OXA-147OXA-10ES-OXAP. aeruginosaA418.1FJ848783UP
Open in a separate windowaThe nomenclature is in accordance with that provided by G. Jacoby on the Lahey website (http://www.lahey.org/Studies/other.asp#table1). Lacking variants (in boldface) are those for which a number has been assigned on this website but for which no information is yet available.bA, acquired; N, natural.c+, the oxacillinase gene was found to be associated with an integron-borne gene cassette; −, the gene is not associated with an integron-borne gene cassette.dExperimentally obtained pI values (when available) versus calculated values. Theoretical values were calculated using software found at the ExPASy proteomics tools website (http://www.expasy.ch/tools/) and the amino acid sequences of the mature proteins only. Peptide cleavage site identification was performed with SignalP (http://www.cbs.dtu.dk/services/SignalP/), and pI computing was performed with the Compute pI/Mw tool (http://www.expasy.ch/tools/pi_tool.html).eUP, unpublished.  相似文献   

11.
Purpose: The study aimed to elucidate the meaning of acceptance in relation to the lived body and sense of self when entering a pain rehabilitation programme. Methods: Six women and three men with long-term pain were interviewed. The interviews were analysed according to interpretative phenomenological analysis. Results: The analysis revealed three different meaning structures, first: acceptance as a process of personal empowerment, “the only way forward”. Here, the individuals expressed that the body felt integrated: a trusting cooperation between self and body gave rise to hope. Second: acceptance as an equivocal project, a possible but challenging way forward. The hopeful insight was there, acknowledging that acceptance was the way to move forward, but there was also uncertainty and doubt about one’s ability with a body ambiguous and confusing, difficult but important to understand. Third, in acceptance as a threat and a personal failure, “no way forward” the integration of the aching body in sense of self was impossible and pain was incomprehensible, unacceptable and unfair. Pain was the cause of feeling stuck in the body, affecting the sense of self and the person’s entire life. Conclusions: The meaning of acceptance was related to acceptance of the persistency of pain, to how the individual related to the lived body and the need for changes in core aspects of self, and to the issue of whether to include others in the struggle of learning to move on with a meaningful life.
  • Implications for Rehabilitation
  • Healthcare professionals should be aware that individuals with long-term pain conceptualize and hold different meanings of acceptance when starting rehabilitation; this should be considered and addressed in rehabilitation programmes.

  • The meaning given to acceptance is related to the experience of the lived body and the sense of self, as well as to getting legitimization/acceptance by others; therefore these aspects need to be considered during rehabilitation.

  • The process of achieving acceptance seems to embrace different processes which can be understood as, and facilitated by, an embodied learning process.

  • The bodily existential challenges presented in the present study, for example to develop an integrated and cooperative relationship with the painful body, can inspire health professionals to develop interventions and communication strategies focusing on the lived body. A wide range of competencies in rehabilitation clinics seems to be needed.

  相似文献   

12.
13.
Background:Hypertension,diabetesaremainriskfactorsofcardiovasculardiseases.Manydatashows:hypertensionmorbidityrateofdiabetespatientsisapparentlyhigherthanthatofnon-diabetespeople.Inforeigncountry,hypertensionmorbidityrateofdiabetespatientsreaches40%~80%.Inourcountry,surveyof220thousandpeoplein1994showedthathypertensionmorbidityrateofdiabetespatientsis55.4%.insulinresistanceiscommonpathogeneticfoundationofhypertensionandtype2diabetes.Inpreviousreports,therewasli…  相似文献   

14.
Avibactam, a non-β-lactam β-lactamase inhibitor with activity against extended-spectrum β-lactamases (ESBLs), KPC, AmpC, and some OXA enzymes, extends the antibacterial activity of ceftazidime against most ceftazidime-resistant organisms producing these enzymes. In this study, the bactericidal activity of ceftazidime-avibactam against 18 Pseudomonas aeruginosa isolates and 15 Enterobacteriaceae isolates, including wild-type isolates and ESBL, KPC, and/or AmpC producers, was evaluated. Ceftazidime-avibactam MICs (0.016 to 32 μg/ml) were lower than those for ceftazidime alone (0.06 to ≥256 μg/ml) against all isolates except for 2 P. aeruginosa isolates (1 blaVIM-positive isolate and 1 blaOXA-23-positive isolate). The minimum bactericidal concentration/MIC ratios of ceftazidime-avibactam were ≤4 for all isolates, indicating bactericidal activity. Human serum and human serum albumin had a minimal effect on ceftazidime-avibactam MICs. Ceftazidime-avibactam time-kill kinetics were evaluated at low MIC multiples and showed time-dependent reductions in the number of CFU/ml from 0 to 6 h for all strains tested. A ≥3-log10 decrease in the number of CFU/ml was observed at 6 h for all Enterobacteriaceae, and a 2-log10 reduction in the number of CFU/ml was observed at 6 h for 3 of the 6 P. aeruginosa isolates. Regrowth was noted at 24 h for some of the isolates tested in time-kill assays. These data demonstrate the potent bactericidal activity of ceftazidime-avibactam and support the continued clinical development of ceftazidime-avibactam as a new treatment option for infections caused by Enterobacteriaceae and P. aeruginosa, including isolates resistant to ceftazidime by mechanisms dependent on avibactam-sensitive β-lactamases.  相似文献   

15.

Background

There is growing public and legislative body support for the medical use of cannabis products, for example, for chemotherapy-induced nausea and vomiting (CINV), in Germany.

Methods

A comprehensive literature search until November 2015 was conducted in MEDLINE, DARE and Cochrane libraries for systematic reviews of randomized controlled trials (RCTs) comparing herbal or pharmaceutical cannabinoids (CB) versus placebo or conventional antiemetics for CINV. Outcomes were reduction of CINV for efficacy, drop-out rates due to adverse events for tolerability, and serious adverse events for safety. The methodology quality of the systematic reviews was evaluated by the tool assessment of multiple systematic reviews (AMSTAR).

Results

Six systematic reviews of RCTs included the pharmaceutical CBs dronabinol, levonantradol, and nabilone or whole plant extract (e.g., nabiximol) compared with placebo or conventional antiemetics. There was moderate quality evidence on the efficacy of CBs compared to placebo and conventional antiemetics for CINV. There was moderate quality evidence that pharmaceutical CBs were less tolerated and less safe than placebo and conventional antiemetics in CINV. One RCT examining whole plant extract was included into the systematic reviews. No RCT was found comparing CBs with neurokinine?1 receptor antagonists.

Conclusions

With safe and effective antiemetics available, CBs cannot be recommended as first- or second-line therapy for CINV. Some guidelines recommend pharmaceutical CBs as third-line treatment in the management of breakthrough nausea and vomiting. Due to the lack of RCT data and safety concerns, herbal cannabis cannot be recommended for CINV.
  相似文献   

16.

Objective

To investigate the extent to which physical performance measures of strength, balance, and mobility taken at discharge from inpatient stroke rehabilitation can predict health-related quality of life (HRQoL) and community reintegration after 6 months.

Design

Longitudinal study.

Setting

University laboratory.

Participants

Adults (N=75) recruited within 1 month of discharge home from inpatient stroke rehabilitation.

Interventions

Not applicable.

Main Outcome Measures

36-Item Short Form Health Survey (SF-36) for HRQoL and Subjective Index of Physical and Social Outcome (SIPSO) for community reintegration. Physical performance measures were the 6-minute walk test, timed Up and Go (TUG) test, Berg Balance Scale, Community Balance and Mobility Scale, and isokinetic torque and power of hip, knee, and ankle on the paretic and nonparetic sides. Other prognostic variables included age, sex, stroke type and location, comorbidities, and motor FIM score.

Results

Separate stepwise linear regressions were performed using the SF-36 and SIPSO as dependent variables. The total paretic lower limb torque and 6-minute walk test predicted the SF-36 Physical Component Summary (adjusted R2=.30). The total paretic lower limb torque and TUG test predicted the SIPSO physical component (adjusted R2=.47). The total paretic lower limb torque significantly predicted the SF-36 Mental Component Summary, but the adjusted R2 was low (.06). Similarly, the TUG test significantly predicted the SIPSO social component, but again the adjusted R2 was low (.09).

Conclusions

Measures of physical performance including muscle strength and mobility at discharge can partially predict HRQoL and community reintegration 6 months later. Further research is necessary for more accurate predictions.  相似文献   

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Nicholas MK  Asghari A 《Pain》2006,124(3):269-279
Research on the role of acceptance in adjustment to persisting pain has been facilitated by the development of the Chronic Pain Acceptance Questionnaire (CPAQ). However, to date the CPAQ has been used to explore acceptance of pain without taking into account the likely contribution of other cognitive variables that have been shown to influence adjustment to persisting pain. This study examined the role of pain acceptance, as measured by the CPAQ, in accounting for adjustment to pain when controlling for the effects of other cognitive variables. The results indicated that while the Activity engagement subscale of the CPAQ was predictive of depression severity, neither of the CPAQ's two subscales was predictive of pain severity or physical disability. These findings differ from some reported previously and they suggest that the CPAQ, by itself, may not be sufficient to explain the processes of acceptance of pain and, hence, adjustment to pain. The findings also indicate that the Pain willingness subscale of the CPAQ is not robust and should be discarded. A broader approach to investigating acceptance of pain is proposed.  相似文献   

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This study looked at the relationship between ratings of the perceived effectiveness of 24 methods for telling the future, 39 complementary therapies (CM) and 12 specific attitude statements about science and medicine. A total of 159 participants took part. The results showed that the participants were deeply sceptical of the effectiveness of the methods for telling the future which factored into meaningful and interpretable factors. Participants were much more positive about particular, but not all, specialties of complementary medicine (CM). These also factored into a meaningful factor structure. Finally, the 12 attitude to science/medicine statements revealed four factors: scepticism of medicine; the importance of psychological factors; patient protection; and the importance of scientific evaluation. Regressional analysis showed that belief in the total effectiveness of different ways of predicting the future was best predicted by beliefs in the effectiveness of the CM therapies. Although interest in the occult was associated with interest in CM, participants were able to distinguish between the two, and displayed scepticism about the effectiveness of methods of predicting the future and some CM therapies.  相似文献   

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