RESUMO
Pediatric Early Warning Scores are advocated to assist health professionals to identify early signs of serious illness or deterioration in hospitalized children. Scores are derived from the weighting applied to recorded vital signs and clinical observations reflecting deviation from a predetermined "norm." Higher aggregate scores trigger an escalation in care aimed at preventing critical deterioration. Process errors made while recording these data, including plotting or calculation errors, have the potential to impede the reliability of the score. To test this hypothesis, we conducted a controlled study of documentation using five clinical vignettes. We measured the accuracy of vital sign recording, score calculation, and time taken to complete documentation using a handheld electronic physiological surveillance system, VitalPAC Pediatric, compared with traditional paper-based charts. We explored the user acceptability of both methods using a Web-based survey. Twenty-three staff participated in the controlled study. The electronic physiological surveillance system improved the accuracy of vital sign recording, 98.5% versus 85.6%, P < .02, Pediatric Early Warning Score calculation, 94.6% versus 55.7%, P < .02, and saved time, 68 versus 98 seconds, compared with paper-based documentation, P < .002. Twenty-nine staff completed the Web-based survey. They perceived that the electronic physiological surveillance system offered safety benefits by reducing human error while providing instant visibility of recorded data to the entire clinical team.
Assuntos
Diagnóstico por Computador/métodos , Documentação/normas , Monitorização Fisiológica/normas , Diagnóstico por Computador/normas , Diagnóstico por Computador/estatística & dados numéricos , Documentação/métodos , Documentação/estatística & dados numéricos , Inglaterra , Indicadores Básicos de Saúde , Humanos , Monitorização Fisiológica/métodos , Monitorização Fisiológica/estatística & dados numéricos , Estudos Prospectivos , Reprodutibilidade dos Testes , Inquéritos e Questionários , Fatores de Tempo , Sinais VitaisRESUMO
BACKGROUND: In-ambulance telemedicine is a recently developed and a promising approach to improve emergency care. We implemented the first ever 24/7 in-ambulance telemedicine service for acute stroke. We report on our experiences with the development and pilot testing of the Prehospital Stroke Study at the Universitair Ziekenhuis Brussel (PreSSUB) to facilitate a wider spread of the knowledge regarding this technique. METHODS: Successful execution of the project involved the development and validation of a novel stroke scale, design and creation of specific hardware and software solutions, execution of field tests for mobile internet connectivity, design of new care processes and information flows, recurrent training of all professional caregivers involved in acute stroke management, extensive testing on healthy volunteers, organisation of a 24/7 teleconsultation service by trained stroke experts and 24/7 technical support, and resolution of several legal issues. RESULTS: In all, it took 41 months of research and development to confirm the safety, technical feasibility, reliability, and user acceptance of the PreSSUB approach. Stroke-specific key information can be collected safely and reliably before and during ambulance transportation and can adequately be communicated with the inhospital team awaiting the patient. CONCLUSION: This paper portrays the key steps required and the lessons learned for successful implementation of a 24/7 expert telemedicine service supporting patients with acute stroke during ambulance transportation to the hospital.
Assuntos
Ambulâncias/organização & administração , Prestação Integrada de Cuidados de Saúde/organização & administração , Diagnóstico por Computador , Acessibilidade aos Serviços de Saúde/organização & administração , Consulta Remota/organização & administração , Acidente Vascular Cerebral/terapia , Terapia Assistida por Computador/organização & administração , Ambulâncias/normas , Bélgica , Benchmarking , Procedimentos Clínicos/organização & administração , Prestação Integrada de Cuidados de Saúde/normas , Diagnóstico por Computador/normas , Acessibilidade aos Serviços de Saúde/normas , Humanos , Modelos Organizacionais , Segurança do Paciente , Projetos Piloto , Avaliação de Programas e Projetos de Saúde , Consulta Remota/normas , Acidente Vascular Cerebral/diagnóstico , Terapia Assistida por Computador/normas , Fatores de Tempo , Resultado do TratamentoRESUMO
Spirometry is a simple test and considered the gold standard in lung function. An obstructive ventilatory defect is a disproportionate reduction of maximal airflow from the lung in relation to the maximal volume that can be displaced from the lung. It implies airway narrowing and is defined by a reduced FEV1/FVC ratio below the 5th percentile of the predicted value (lower limit of normal, LLN). A restrictive disorder may be suspected when vital capacity (FVC) is reduced and FEV1/FVC is normal. It is definitely proven, however, only by a decrease in TLC below the 5th percentile of predicted value (LLN). The measurement of TLC by body plethysmography is necessary to confirm or exclude a restrictive defect or hyperinflation of the lung when FVC is below the LLN. 2012 a task force of the ERS published new reference values based on 74,187 records from healthy non-smoking males and females from 26 countries. The new reference equations for the 3-95 age range are now available that include appropriate age-dependent mean values and lower limits of normal (LLN). This presentation aims at providing the reader with recommendations dealing with standardization and interpretation of spirometry.
Assuntos
Diagnóstico por Computador/normas , Medicina Ambiental/normas , Medicina do Trabalho/normas , Guias de Prática Clínica como Assunto , Pneumologia/normas , Espirometria/normas , AlemanhaRESUMO
BACKGROUND: It has been suggested that, in order to validate a diagnosis of (C)APD (central auditory processing disorder), testing using direct cross-modal analogs should be performed to demonstrate that deficits exist solely or primarily in the auditory modality (McFarland and Cacace, 1995; Cacace and McFarland, 2005). This modality-specific viewpoint is controversial and not universally accepted (American Speech-Language-Hearing Association [ASHA], 2005; Musiek et al, 2005). Further, no such analogs have been developed to date, and neither the feasibility of such testing in normally functioning individuals nor the concurrent validity of cross-modal analogs has been established. PURPOSE: The purpose of this study was to investigate the feasibility of cross-modal testing by examining the performance of normal adults and children on four tests of central auditory function and their corresponding visual analogs. In addition, this study investigated the degree to which concurrent validity of auditory and visual versions of these tests could be demonstrated. RESEARCH DESIGN: An experimental repeated measures design was employed. STUDY SAMPLE: Participants consisted of two groups (adults, n=10; children, n=10) with normal and symmetrical hearing sensitivity, normal or corrected-to-normal visual acuity, and no family or personal history of auditory/otologic, language, learning, neurologic, or related disorders. DATA COLLECTION AND ANALYSIS: Visual analogs of four tests in common clinical use for the diagnosis of (C)APD were developed (Dichotic Digits [Musiek, 1983]; Frequency Patterns [Pinheiro and Ptacek, 1971]; Duration Patterns [Pinheiro and Musiek, 1985]; and the Random Gap Detection Test [RGDT; Keith, 2000]). Participants underwent two 1 hr test sessions separated by at least 1 wk. Order of sessions (auditory, visual) and tests within each session were counterbalanced across participants. ANOVAs (analyses of variance) were used to examine effects of group, modality, and laterality (for the Dichotic/Dichoptic Digits tests) or response condition (for the auditory and visual Frequency Patterns and Duration Patterns tests). Pearson product-moment correlations were used to investigate relationships between auditory and visual performance. RESULTS: Adults performed significantly better than children on the Dichotic/Dichoptic Digits tests. Results also revealed a significant effect of modality, with auditory better than visual, and a significant modality×laterality interaction, with a right-ear advantage seen for the auditory task and a left-visual-field advantage seen for the visual task. For the Frequency Patterns test and its visual analog, results revealed a significant modality×response condition interaction, with humming better than labeling for the auditory version but the reversed effect for the visual version. For Duration Patterns testing, visual performance was significantly poorer than auditory performance. Due to poor test-retest reliability and ceiling effects for the auditory and visual gap-detection tasks, analyses could not be performed. No cross-modal correlations were observed for any test. CONCLUSIONS: Results demonstrated that cross-modal testing is at least feasible using easily accessible computer hardware and software. The lack of any cross-modal correlations suggests independent processing mechanisms for auditory and visual versions of each task. Examination of performance in individuals with central auditory and pan-sensory disorders is needed to determine the utility of cross-modal analogs in the differential diagnosis of (C)APD.
Assuntos
Estimulação Acústica , Diagnóstico por Computador/normas , Testes com Listas de Dissílabos/normas , Transtornos do Desenvolvimento da Linguagem/diagnóstico , Estimulação Luminosa , Adolescente , Adulto , Fatores Etários , Limiar Auditivo , Criança , Diagnóstico Diferencial , Estudos de Viabilidade , Humanos , Valores de Referência , Adulto JovemRESUMO
OBJECTIVES: Many new processing features in hearing aids have their primary effects on information located in the high frequencies. Speech perception tests that are optimized for evaluating high-frequency processing are needed to adequately study its effects on speech identification. The goal of the current research was to develop a medium for evaluating the effects of high-frequency processing in hearing aids. DESIGN: A list of 115 consonant-vowel-consonant-vowel-consonant nonsense syllables with American English consonants in all word positions was created in an open-set phoneme identification format. The source material was spoken by a male and a female speaker. A custom computer program was developed for administration of the test and automatic analysis of the test results. Nine normal-hearing listeners were employed in the collection of the normative data. The test was presented to the listeners in quiet (at 68 dB SPL), in noise at five signal-to-noise ratios (SNRs; -10, -5, 0, 5, and 10), and in a low-pass filter condition with cutoff frequencies at 500, 1000, 1500, 2000, and 4000 Hz. The data were examined to evaluate the psychometric properties of the test for different phoneme positions and phoneme classes. In addition, a shortened version of the test was developed based on the data from normal-hearing listeners. The test-retest reliability was verified at 0 dB SNR. The full and shortened versions of the test were repeated in 10 hearing-impaired listeners at their most comfortable listening level in quiet and in noise at various SNRs. RESULTS: The availability of high-frequency output was verified with acoustic analysis. The performance intensity functions for both versions of the test (i.e., male and female speakers) showed expected monotonic growth with SNR and cutoff frequencies. High reliability was seen between test and retest identification scores in normal-hearing and hearing-impaired listeners. CONCLUSIONS: The current nonsense syllable test provided a reliable and efficient means for phoneme identification testing.
Assuntos
Correção de Deficiência Auditiva/métodos , Correção de Deficiência Auditiva/normas , Perda Auditiva/reabilitação , Testes de Discriminação da Fala/métodos , Testes de Discriminação da Fala/normas , Inteligibilidade da Fala , Estimulação Acústica/métodos , Estimulação Acústica/normas , Adulto , Diagnóstico por Computador/métodos , Diagnóstico por Computador/normas , Feminino , Auxiliares de Audição , Perda Auditiva/diagnóstico , Humanos , Masculino , Fonética , Discriminação da Altura Tonal , Software , Percepção da Fala , Adulto JovemRESUMO
The aim of the study was to test a new stabilometric platform (BioGP) designed to provide visual feedback to patients with balance disorders performing sustained voluntary shifts of their center of pressure (COP). Twenty-five outpatients with mild to moderate impairments of balance due to multiple sclerosis (MS) and 23 healthy subjects volunteered for the study. Patients' control of balance in static conditions was first rated on the Ataxia Battery and the Motricity Index; all subjects were then asked to stand on the platform in front of a large screen and try to move a visual target representing the momentary position of their COP along two vertical paths and one horizontal paths by appropriate movements of their hips and ankles along the lateral and antero-posterior planes. To assess the validity of BioGP, clinical scores of static balance were correlated with measures of speed and accuracy on the platform tasks. To assess the sensitivity of the equipment to poor balance control, patients' measures were compared with those of healthy subjects. Pearson's correlation coefficients between the Ataxia Battery scores and BioGP data ranged between -0.4 and - 0.82. As a group, patients performed statistically worse than controls on most BioGP measures. The graphic output of BioGP also contributed to define the dynamic relations between momentary COP position and balance control. These preliminary findings suggest a possible use of the system as both an evaluation and rehabilitation instrument.
Assuntos
Biorretroalimentação Psicológica/instrumentação , Diagnóstico por Computador/instrumentação , Esclerose Múltipla/fisiopatologia , Equilíbrio Postural , Adulto , Estudos de Casos e Controles , Diagnóstico por Computador/normas , Desenho de Equipamento , Feminino , Humanos , Masculino , Esclerose Múltipla/psicologia , Esclerose Múltipla/reabilitação , Neurologia/instrumentação , Projetos Piloto , Pressão , Reabilitação/instrumentação , VoliçãoRESUMO
OBJECTIVE: To ascertain the incidence of asymmetry of the occipital condyles. The a priori hypothesis of symmetry (which is pervasive both in the determination of "subluxation" and in the means chosen for correction) was tested. DESIGN: Data set design was used with a convenience sample. The condyles were chosen for convenience of visualization from plain film radiographs. The study was retrospectively designed, albeit with prospective implications for analytic investigation. SETTING: The research department of Cleveland Chiropractic College, Kansas City, MO. PATIENTS OR OTHER PARTICIPANTS: One hundred fifty-one submentovertex radiographs were examined using a computer-assisted digitizer. The radiographs were randomly obtained from the patient files of two doctors of chiropractic who routinely use this type of radiograph in their patient analysis. INTERVENTIONS: The study was a side-to-side comparison of the condyles, which were subject to neither intervention nor change. MAIN OUTCOME MEASURES: Surface area of left and right condyles for 151 examined pairs. RESULTS: Analysis with Pearson's correlation coefficient implied a lack of symmetry between condyles (r = .37; p < .0001). The scatterplot revealed values widely dispersed about the regression line, and the standard error of the estimate was 36.7. CONCLUSION: The data suggest that the underlying premise of symmetry in chiropractic analysis needs to be reexamined.
Assuntos
Articulação Atlantoccipital , Diagnóstico por Computador/normas , Luxações Articulares/diagnóstico por imagem , Antropometria , Quiroprática , Diagnóstico por Computador/métodos , Humanos , Incidência , Luxações Articulares/epidemiologia , Luxações Articulares/patologia , Missouri/epidemiologia , Radiografia , Estudos RetrospectivosRESUMO
The purpose of this study was to examine the heart rate patterns before and after a standardized external vibratory acoustic stimulation in a group of 24 healthy premature fetuses at 32-35 weeks gestational age. FHR was analysed on line by Sonicaid Computer System 8000. A significant increase in the number of accelerations and an increase of variation after stimulus were observed. All other FHR patterns such as baseline, high and low episodes did not change significantly.