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1.
Front Rehabil Sci ; 3: 964613, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-36189022

RESUMO

Background: Rehabilitation is the key to management of patients with subacromial impingement syndrome to prevent disability and loss of function. While point-of-care musculoskeletal ultrasound aids clinical diagnosis of subacromial impingement syndrome, many patients do not demonstrate the classic findings of dynamic supraspinatus tendon impingement beneath the acromion on ultrasound. The objective of this study was to establish the most reliable shoulder ultrasound measurements for subacromial impingement, by evaluating the intra-rater and inter-rater reliability of measurements in asymptomatic participants. Methods: Eighteen participants (9 women, 9 men, mean ± standard deviation: 34.6 ± 7.9 years of age) underwent bilateral shoulder ultrasound evaluations with measurements for subacromial impingement (acromiohumeral distance, acromion-greater tuberosity distance, supraspinatus tendon, subacromial-subdeltoid bursa, and subacromial-subdeltoid bursal fluid thickness) performed by two sports medicine physicians. Intra-class coefficients were calculated to determine the intra- and inter-rater reliability of shoulder ultrasound images and measurements. Results: Intra-rater reliability for acromiohumeral distance (0.76-0.79), supraspinatus tendon (0.91-0.95), subacromial-subdeltoid bursa (0.76-0.84), and subacromial-subdeltoid bursal fluid thickness (0.75-0.81) was found to be good to excellent, whereas inter-rater reliability ranged from poor to moderate. Conclusions: Acromiohumeral distance in neutral position and short axis ultrasound measurements of supraspinatus tendon, subacromial-subdeltoid bursa, and subacromial-subdeltoid bursal fluid thickness in the modified Crass position were the most reliable for subacromial impingement in asymptomatic participants. We recommend validation of these measurements in a symptomatic population to aid diagnosis and direct rehabilitation of patients with suspected subacromial impingement, and to increase point-of-care ultrasound uptake, availability, and training among rehabilitation professionals across health systems.

2.
Pediatr Ann ; 50(11): e454-e460, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34757874

RESUMO

The coronavirus disease 2019 (COVID-19) pandemic has brought to forefront the large morbidity, mortality, and complications that viral illnesses can cause. For athletes, viral illnesses can be disruptive toward their participation in youth sports. This article outlines the details of how the most common viral illnesses affect the youth athlete and youth sports, including COVID-19, non-COVID-19 upper respiratory infections, influenza, Epstein-Barr virus, varicella, herpes, and other dermatologic infections. In this article, we review current available guidelines and recommendations on how to handle these infections in athletes during sports as well as return-to-play recommendations. [Pediatr Ann. 2021;50(11):e454-e460.].


Assuntos
Atletas , COVID-19 , Viroses/prevenção & controle , Esportes Juvenis , Adolescente , Humanos , Controle de Infecções , SARS-CoV-2
3.
Clin Imaging ; 55: 161-164, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30897383

RESUMO

We present two cases of atraumatic costal cartilage fracture secondary to violent coughing. Although costal cartilage fractures due to trauma and bony rib fractures due to violent coughing have been described, to our knowledge there have been no prior reported cases of cough-induced costal cartilage fracture. It is important for radiologists to consider costal cartilage fractures, which are often more subtle than osseous injuries, in patients with chest pain, and understand that they may not always be preceded by direct trauma. Identifying this injury is clinically important and will prevent patients from undergoing unnecessary examinations to rule out a cardiac cause of chest pain or a pulmonary embolism.


Assuntos
Cartilagem Costal/lesões , Tosse/complicações , Fraturas de Cartilagem/etiologia , Idoso , Dor no Peito/etiologia , Cartilagem Costal/diagnóstico por imagem , Fraturas de Cartilagem/diagnóstico por imagem , Humanos , Masculino , Pessoa de Meia-Idade , Fraturas das Costelas/diagnóstico por imagem , Fraturas das Costelas/etiologia , Costelas/diagnóstico por imagem , Costelas/lesões , Tomografia Computadorizada por Raios X/métodos
5.
J Cell Mol Med ; 15(4): 747-55, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-20406327

RESUMO

Parkinson's disease (PD) is a neurodegenerative disorder caused by the loss of dopaminergic neurons. Adult human endometrial derived stem cells (HEDSC), a readily obtainable type of mesenchymal stem-like cell, were used to generate dopaminergic cells and for transplantation. Cells expressing CD90, platelet derived growth factor (PDGF)-Rß and CD146 but not CD45 or CD31 were differentiated in vitro into dopaminergic neurons that exhibited axon projections, pyramidal cell bodies and dendritic projections that recapitulate synapse formation; these cells also expressed the neural marker nestin and tyrosine hydroxylase, the rate-limiting enzyme in dopamine synthesis. Whole cell patch clamp recording identified G-protein coupled inwardly rectifying potassium current 2 channels characteristic of central neurons. A 1-methyl 4-phenyl 1,2,3,6-tetrahydro pyridine induced animal model of PD was used to demonstrate the ability of labelled HEDSC to engraft, migrate to the site of lesion, differentiate in vivo and significantly increase striatal dopamine and dopamine metabolite concentrations. HEDSC are a highly inducible source of allogenic stem cells that rescue dopamine concentrations in an immunocompetent PD mouse model.


Assuntos
Dopamina/biossíntese , Endométrio/citologia , Doença de Parkinson/metabolismo , Doença de Parkinson/terapia , Transplante de Células-Tronco , Células-Tronco/citologia , Adulto , Animais , Diferenciação Celular , Movimento Celular , Modelos Animais de Doenças , Fenômenos Eletrofisiológicos , Feminino , Citometria de Fluxo , Humanos , Camundongos , Neostriado/metabolismo , Neostriado/patologia , Neurogênese , Células-Tronco/metabolismo
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