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3.
J Am Acad Dermatol ; 81(6): 1277-1282, 2019 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-30991120

RESUMO

BACKGROUND: Klippel-Trenaunay syndrome (KTS) is a vascular malformation overgrowth syndrome characterized by capillary malformation, venous malformation, and limb overgrowth, with or without lymphatic malformation. Patients are at an increased risk of hemorrhage and venous thromboembolism (VTE). Consequently, women with this condition often are counseled to avoid pregnancy, but minimal data are available on the relationship between pregnancy, VTE, and bleeding risk. OBJECTIVE: To review the risk of VTE and bleeding in pregnant and nulligravid women with KTS. METHODS: A retrospective medical record review was performed of women with KTS, aged ≥18 years, evaluated at Mayo Clinic Rochester, Minnesota, from August 1945 to April 2018. RESULTS: We identified 75 women with ≥1 pregnancy and 64 nulligravid women. VTE prevalence was 14 of 70 (20%) for women with a history of pregnancy and 16 of 64 (25%) for nulligravid women (P = .93). Among the 70 women with a history of pregnancy, 7 of 18 VTE events (39%) occurred in association with pregnancy, with VTE affecting 7 of 151 pregnancies (4.6%). Significant bleeding prevalence was 6 of 70 (8.6%) for women with a history of pregnancy and 6 of 64 (9.4%) for nulligravid women (P = .54). LIMITATIONS: This was a retrospective review. CONCLUSION: The prevalence of VTE and bleeding was similar in patients with KTS, irrespective of pregnancy status.


Assuntos
Hemorragia/etiologia , Síndrome de Klippel-Trenaunay-Weber/diagnóstico , Resultado da Gravidez , Gravidez de Alto Risco , Tromboembolia Venosa/etiologia , Centros Médicos Acadêmicos , Adulto , Estudos de Coortes , Bases de Dados Factuais , Feminino , Hemorragia/diagnóstico , Hemorragia/epidemiologia , Humanos , Síndrome de Klippel-Trenaunay-Weber/complicações , Gravidez , Complicações na Gravidez/diagnóstico , Complicações na Gravidez/mortalidade , Embolia Pulmonar/epidemiologia , Embolia Pulmonar/etiologia , Embolia Pulmonar/fisiopatologia , Estudos Retrospectivos , Medição de Risco , Taxa de Sobrevida , Malformações Vasculares/complicações , Malformações Vasculares/diagnóstico , Tromboembolia Venosa/diagnóstico , Tromboembolia Venosa/terapia , Adulto Jovem
4.
Curr Biol ; 27(17): 2684-2691.e7, 2017 Sep 11.
Artigo em Inglês | MEDLINE | ID: mdl-28844645

RESUMO

Prior research using functional magnetic resonance imaging (fMRI) [1-4] and behavioral studies of patients with acquired or congenital amusia [5-8] suggest that the right posterior superior temporal gyrus (STG) in the human brain is specialized for aspects of music processing (for review, see [9-12]). Intracranial electrical brain stimulation in awake neurosurgery patients is a powerful means to determine the computations supported by specific brain regions and networks [13-21] because it provides reversible causal evidence with high spatial resolution (for review, see [22, 23]). Prior intracranial stimulation or cortical cooling studies have investigated musical abilities related to reading music scores [13, 14] and singing familiar songs [24, 25]. However, individuals with amusia (congenitally, or from a brain injury) have difficulty humming melodies but can be spared for singing familiar songs with familiar lyrics [26]. Here we report a detailed study of a musician with a low-grade tumor in the right temporal lobe. Functional MRI was used pre-operatively to localize music processing to the right STG, and the patient subsequently underwent awake intraoperative mapping using direct electrical stimulation during a melody repetition task. Stimulation of the right STG induced "music arrest" and errors in pitch but did not affect language processing. These findings provide causal evidence for the functional segregation of music and language processing in the human brain and confirm a specific role of the right STG in melody processing. VIDEO ABSTRACT.


Assuntos
Percepção Auditiva/fisiologia , Transtornos da Percepção Auditiva/fisiopatologia , Lobo Temporal/fisiopatologia , Adulto , Transtornos da Percepção Auditiva/etiologia , Neoplasias Encefálicas/complicações , Estimulação Elétrica , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Música , Adulto Jovem
6.
J AAPOS ; 17(4): 385-90, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23993718

RESUMO

PURPOSE: To identify barriers to follow-up eye care in children who failed a visual acuity screening conducted by their primary care provider. METHODS: Children aged 3-14 years who failed a visual acuity screening were identified. A phone survey with the parent of every child was conducted 4 months after the screening. Family demographics, parental awareness of childhood eye diseases and eye care for children, and barriers to follow-up eye care were assessed. RESULTS: Of 971 children sampled, 199 (20.5%) failed a visual acuity screening. The survey was completed by the parents of 58 children (29.1%), of whom 27 (46.6%) presented for follow-up examination. The most common reason for failure to follow-up was parental unawareness of screening results (29.3%). Follow-up rates were higher in children with previous eye examinations than in those without (81% versus 17%; P = 0.005) and in children who waited <2 months for a follow-up appointment than in those who had to wait longer (100% versus 63%; P = 0.024). Child's sex, ethnicity, and health insurance status, parent's marital, education and employment status, household income, and transportation access were not associated with statistically significant different follow-up rates. CONCLUSIONS: Parental unawareness of a failed visual acuity screening is an important barrier to obtaining follow-up. Strategies to improve follow-up rates after a failed visual acuity screening may include communicating the results clearly and consistently, providing education about the importance of timely follow-up, and offering logistic support for accessing eye appointments to families.


Assuntos
Acesso aos Serviços de Saúde/normas , Aceitação pelo Paciente de Cuidados de Saúde , Transtornos da Visão/diagnóstico , Seleção Visual/organização & administração , Adolescente , Criança , Pré-Escolar , Connecticut , Feminino , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Masculino , Pais , Atenção Primária à Saúde/organização & administração , Fatores de Risco , Inquéritos e Questionários
7.
J Acoust Soc Am ; 119(2): 719-22, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16521731

RESUMO

Absolute pitch is extremely rare in the U.S. and Europe; this rarity has so far been unexplained. This paper reports a substantial difference in the prevalence of absolute pitch in two normal populations, in a large-scale study employing an on-site test, without self-selection from within the target populations. Music conservatory students in the U.S. and China were tested. The Chinese subjects spoke the tone language Mandarin, in which pitch is involved in conveying the meaning of words. The American subjects were nontone language speakers. The earlier the age of onset of musical training, the greater the prevalence of absolute pitch; however, its prevalence was far greater among the Chinese than the U.S. students for each level of age of onset of musical training. The findings suggest that the potential for acquiring absolute pitch may be universal, and may be realized by enabling infants to associate pitches with verbal labels during the critical period for acquisition of features of their native language.


Assuntos
Idioma , Percepção da Altura Sonora/fisiologia , Acústica da Fala , Adolescente , Adulto , China , Etnicidade , Feminino , Humanos , Masculino , Música , Prevalência , Estudantes , Estados Unidos
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