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1.
Int J Cardiol Heart Vasc ; 40: 100995, 2022 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-35345773

RESUMO

Background: Persistent dyspnea and reduced exercise capacity is common in pulmonary embolism (PE) survivors. Although improved right ventricular function after pulmonary rehabilitation has been demonstrated in chronic thromboembolic pulmonary hypertension, it is still unknown whether a similar effect also occurs in other patients with dyspnea after pulmonary embolism. Purpose: The aim of this study was to explore potential effects of a pulmonary rehabilitation program on cardiac structure and function as assessed with cardiac magnetic resonance (CMR). Material and methods: Twenty-six PE survivors with persistent dyspnea were included. Right and left ventricular assessment with CMR was performed before and after an eight-week pulmonary rehabilitation program. Results: Dyspnea as measured by the Shortness of Breath Questionnaire improved significantly after rehabilitation: 15 (IQR: 7-31) versus 8 (IQR: 3-17). Absolute right ventricular global longitudinal strain by CMR was reduced from 19% to 18% (95% CI of difference: 0-3 percent points), and absolute RV lateral strain from 26% to 24% (95% CI of difference: 1-4 percent points). Right ventricular mass was reduced after rehabilitation from 49 g to 44 g (95% CI of difference: 2-8 g). Conclusion: Although there was a substantial improvement in dyspnea after rehabilitation, we found only a minor reduction in absolute right ventricular longitudinal strain and right ventricular mass. No other CMR parameter changed. We therefore suggest that rehabilitation effect of in this patient group was not primarily mediated by cardiac adaptions.

2.
J Thromb Haemost ; 16(12): 2471-2481, 2018 12.
Artigo em Inglês | MEDLINE | ID: mdl-30303610

RESUMO

Essentials The aim of deep vein thrombosis (DVT) diagnostic work-up is to maximize both safety and efficiency. We explored whether D-dimer is safe and efficient as a stand-alone test to exclude DVT. Our findings suggest it is a safe, efficient and simplified diagnostic strategy. The safety of age-adjusted D-dimer as a stand-alone test requires further investigation. SUMMARY: Background Several strategies for safely excluding deep vein thrombosis (DVT) while limiting the number of imaging tests have been explored. Objectives To determine whether D-dimer testing could safely and efficiently exclude DVT as a stand-alone test, and evaluate its performance as compared with strategies that incorporate the Wells score and age-adjusted D-dimer. Patients/Methods We included consecutive outpatients referred with suspected DVT to the Emergency Department at Østfold Hospital, Norway. STA-Liatest D-Di PLUS D-dimer was analyzed for all patients. Patients with a D-dimer level of ≥ 0.5 µg mL-1 were referred for compression ultrasonography (CUS). In patients with a D-dimer level of < 0.5 µg mL-1 , no further testing was performed and anticoagulation was withheld. Patients were followed for 3 months for venous thromboembolism (VTE). Results Of the 913 included patients, 298 (33%) had a negative D-dimer result. One hundred and seventy-three patients (18.9%) were diagnosed with DVT at baseline. One of 298 patients had DVT despite having a negative D-dimer result, resulting in a failure rate of 0.3% (95% confidence interval [CI] 0.1-1.9%). Adding the modified Wells score would have yielded a failure rate of 0.0% (95% CI 0.0-1.8%) while necessitating 87 more CUS examinations. Age-adjusted D-dimer as a stand-alone test would have necessitated 80 fewer CUS examinations than fixed D-dimer as a stand-alone test, at the cost of a failure rate of 1.6% (95% CI 0.7-3.4%). Conclusions This outcome study shows that a negative high-sensitivity D-dimer result safely excludes DVT in an outpatient population, and necessitates fewer CUS than if used in combination with Wells score. The safety of stand-alone age-adjusted D-dimer needs further assessment in prospective outcome studies.


Assuntos
Análise Química do Sangue , Produtos de Degradação da Fibrina e do Fibrinogênio/análise , Trombose Venosa/diagnóstico , Idoso , Idoso de 80 Anos ou mais , Assistência Ambulatorial , Biomarcadores/sangue , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Prognóstico , Estudos Prospectivos , Reprodutibilidade dos Testes , Trombose Venosa/sangue
3.
Thromb Res ; 163: 47-50, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29353683

RESUMO

Diagnosing upper extremity deep vein thrombosis (UEDVT) can be challenging. Compression ultrasonography is often inconclusive because of overlying anatomic structures that hamper compressing veins. Contrast venography is invasive and has a risk of contrast allergy. Magnetic Resonance Direct Thrombus Imaging (MRDTI) and Three Dimensional Turbo Spin-echo Spectral Attenuated Inversion Recovery (3D TSE-SPAIR) are both non-contrast-enhanced Magnetic Resonance Imaging (MRI) sequences that can visualize a thrombus directly by the visualization of methemoglobin, which is formed in a fresh blood clot. MRDTI has been proven to be accurate in diagnosing deep venous thrombosis (DVT) of the leg. The primary aim of this pilot study was to test the feasibility of diagnosing UEDVT with these MRI techniques. MRDTI and 3D TSE-SPAIR were performed in 3 pilot patients who were already diagnosed with UEDVT by ultrasonography or contrast venography. In all patients, UEDVT diagnosis could be confirmed by MRDTI and 3D TSE-SPAIR in all vein segments. In conclusion, this study showed that non-contrast MRDTI and 3D TSE-SPAIR sequences may be feasible tests to diagnose UEDVT. However diagnostic accuracy and management studies have to be performed before these techniques can be routinely used in clinical practice.


Assuntos
Imageamento por Ressonância Magnética/métodos , Trombose Venosa Profunda de Membros Superiores/diagnóstico , Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Projetos Piloto
4.
HNO ; 59(12): 1185-90, 2011 Dec.
Artigo em Alemão | MEDLINE | ID: mdl-22159337

RESUMO

Acupuncture as a complementary method provides optimal conditions for ENT specialists, particularly when somatotopic microsystems are used, e.g., ear, skull, and oral acupuncture. Via points of these systems, pain conditions and functional disorders as well as specific ENT indications (e.g., rhinitis pollinosa, sinusitis, pharyngitis) can be treated successfully. Therapy is performed quickly and without side effects.


Assuntos
Terapia por Acupuntura/métodos , Otolaringologia/métodos , Otorrinolaringopatias/terapia , Terapia por Acupuntura/efeitos adversos , Áustria , Humanos , Padrões de Prática Médica , Resultado do Tratamento
5.
Laryngorhinootologie ; 88(12): 799-811; quiz 812-3, 2009 Dec.
Artigo em Alemão | MEDLINE | ID: mdl-20027537

RESUMO

For ENT specialists it is good to become familiar with the basics of acupuncture, as in our times this method of treatment has been spread and accepted worldwide. Modern pain research has succeeded in scientific exploring and verifying acupuncture effects. Any medical specialist having understood the facts and implications of acupuncture as laid out in this paper, may take the chance to try and put acupuncture into practice in his/her daily work. One of the challenges of doctors nowadays is the increase of functional disorders, of myofascial pain syndromes, of patients' general ill-feeling of health. Particularly in pain management, as regards to the considerable toxic by-effects of long-term prescribed analgetics, there is a need of gentle therapies such as acupuncture, free from side-effects. It is the patients who demand alternative concepts. For ENT-doctors running a busy office, microsystem acupuncture in particular may be recommended. Inserting a couple of needles at the auricle, or injecting a few drops into the oral mucosa is a quick action which in most cases will provide beneficial results.


Assuntos
Terapia por Acupuntura , Otorrinolaringopatias/terapia , Pontos de Acupuntura , Acupuntura Auricular , Terapia Combinada , Humanos , Síndromes da Dor Miofascial/terapia , Transtornos Somatoformes/terapia , Resultado do Tratamento
6.
Br Dent J ; 207(12): E26, 2009 Dec 19.
Artigo em Inglês | MEDLINE | ID: mdl-19876045

RESUMO

BACKGROUND: Patients presenting with oromyofacial disorders and pain in the head and neck area are often resistant to conventional therapy. Acupuncture has been shown to be effective in pain reduction. METHODS: Twenty-three patients with craniomandibular disorders, headache and, in particular, local pain in the orofacial, cervical and temporomandibular joint areas were randomised into acupuncture or placebo laser therapy groups. Pain was assessed by a visual analogue scale (VAS) and by palpation of 14 muscles and groups of muscles immediately before and after treatment, the assessor being blinded to the patients' allocation. Applicable acupuncture points were searched and pricked using the 'very-point' technique. FINDINGS: Pain reduction measured by VAS was significantly more pronounced after acupuncture than after placebo treatment (p=0.031). Sum of pain scores across 14 muscles was considerably more reduced after acupuncture as compared to sham laser treatment. INTERPRETATION: Acupuncture may bring about immediate pain relief in patients with oromyofacial disorders, increasing the chance to initiate other therapeutic measures.


Assuntos
Terapia por Acupuntura , Transtornos Craniomandibulares/terapia , Síndrome da Disfunção da Articulação Temporomandibular/terapia , Pontos de Acupuntura , Adolescente , Método Duplo-Cego , Dor Facial/terapia , Feminino , Cefaleia/terapia , Humanos , Lasers , Músculo Masseter/patologia , Músculos do Pescoço/patologia , Cervicalgia/terapia , Medição da Dor , Palpação , Placebos , Músculos Pterigoides/patologia , Músculo Temporal/patologia , Adulto Jovem
7.
BMJ ; 322(7302): 1574-8, 2001 Jun 30.
Artigo em Inglês | MEDLINE | ID: mdl-11431299

RESUMO

OBJECTIVES: To compare the efficacy of acupuncture and conventional massage for the treatment of chronic neck pain. DESIGN: Prospective, randomised, placebo controlled trial. SETTING: Three outpatient departments in Germany. PARTICIPANTS: 177 patients aged 18-85 years with chronic neck pain. INTERVENTIONS: Patients were randomly allocated to five treatments over three weeks with acupuncture (56), massage (60), or "sham" laser acupuncture (61). PRIMARY OUTCOME MEASURE: maximum pain related to motion (visual analogue scale) irrespective of direction of movement one week after treatment. SECONDARY OUTCOME MEASURES: range of motion (3D ultrasound real time motion analyser), pain related to movement in six directions (visual analogue scale), pressure pain threshold (pressure algometer), changes of spontaneous pain, motion related pain, global complaints (seven point scale), and quality of life (SF-36). Assessments were performed before, during, and one week and three months after treatment. Patients' beliefs in treatment were assessed. RESULTS: One week after five treatments the acupuncture group showed a significantly greater improvement in motion related pain compared with massage (difference 24.22 (95% confidence interval 16.5 to 31.9), P=0.0052) but not compared with sham laser (17.28 (10.0 to 24.6), P=0.327). Differences between acupuncture and massage or sham laser were greater in the subgroup who had had pain for longer than five years (n=75) and in patients with myofascial pain syndrome (n=129). The acupuncture group had the best results in most secondary outcome measures. There were no differences in patients' beliefs in treatment. CONCLUSIONS: Acupuncture is an effective short term treatment for patients with chronic neck pain, but there is only limited evidence for long term effects after five treatments.


Assuntos
Analgesia por Acupuntura , Massagem , Cervicalgia/terapia , Adulto , Idoso , Idoso de 80 Anos ou mais , Distribuição de Qui-Quadrado , Doença Crônica , Intervalos de Confiança , Neuralgia Facial/terapia , Feminino , Humanos , Terapia a Laser , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos
8.
Scand J Clin Lab Invest ; 59(1): 33-45, 1999 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-10206096

RESUMO

The EU-AIM project "OpenLabs" specified an open systems architecture for a clinical laboratory information system (LIS) environment and coined the term "open LIS". Since this conception has not yet been realized into systems and modules commercially available, two university hospitals in Norway had to specify an alternative model for openness when they, in a joint project, screened the market for a new LIS. To be open, a LIS must be (1) based on main-trend hardware and system software running under a standardized operating system, (2) designed for network-based distributed computing, (3) have sufficient documentation available to local staff, (4) be configurable through parameters, tables and scripts, and (5) have general and configurable access mechanisms both to real-time processes and to the database. The present study describes the selection process and examines the compliance of the selected LIS (NetLab) with this model of openness. It is shown that local staff have been able to adapt this LIS to various and changing requirements in the laboratory.


Assuntos
Sistemas de Informação , Laboratórios
10.
Zahnarzt ; 22(5): 259-64, 1978 May.
Artigo em Alemão | MEDLINE | ID: mdl-280071
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