Psychophysically determined full-field stimulus thresholds (FST) in retinitis pigmentosa: relationships with electroretinography and visual field outcomes.

PURPOSE: The purpose of this study is to describe the relationships between full-field stimulus threshold (FST), electroretinography (ERG), and visual field (VF) outcomes in retinitis pigmentosa (RP). METHODS: Data from 47 patients with RP (n = 94 eyes) were evaluated. Patients were submitted to comprehensive ophthalmological examination including measurement of best-corrected visual acuity (BCVA), 30-2 threshold static VF, and microperimetry. Full-field ERG (ISCEV standard) was recorded, and achromatic FST was measured using a Diagnosys Espion system with the ColorDome™ LED full-field stimulator (Diagnosys LLC, Lowell, MA, USA). RESULTS: BCVA mean ± SD was 0.31 ± 0.03 logMAR, and FST mean ± SD was -18.45 ± 9.53 dB. No significant correlation was found between BCVA and FST. In contrast, statistically significant correlations were found between FST and static 30-2 VF mean deviation (r = -0.389; P < 0.01), microperimetry mean threshold (r = -0.607; P < 0.01). Dark and light-adapted ERGs were detectable in 28 and 48 eyes, respectively. Nevertheless, considering only the eyes with recordable ERG responses, moderate correlations were found between combined dark-adapted a-wave amplitude (r = -0.560; P < 0.01), b-wave amplitude (r = -0.643; P < 0.001), 30-Hz flicker response (r = -0.501; P < 0.01), and FST, and high correlation with FST for cone b-wave amplitude (r = -0.715; P < 0.01). CONCLUSIONS: FST could be successfully determined in RP patients with a wide range of vision loss. FST results showed stronger correlations with full-field ERG amplitude than with sensitivity measured with visual field tests. FST is as an alternative to VF or ERG for assessment of retinal function in patients unable to do visual fields or with non-detectable ERGs.

Diagnóstico post-mortem de infarto agudo do miocárdio em pacientes com insuficiência respiratória aguda - análise demográfica, etiológica e histológica pulmonar / Post-mortem diagnosis of acute myocardial infarction in patients with acute respiratory failure - demographic,etiologic and histological pulmonary analysis

Introdução: A insuficiência respiratória aguda (IRA) está presente em 5% dos pacientes com infarto agudo do miocárdio (IAM) e é associada à mortalidade de 20% a 30% nesses pacientes. Não está claro o papel da inflamação relacionada ao edemaagudo de pulmão (EAP) na gênese da IRA pós IAM. Objetivos: Descrever os dados demográficos, etiológicos e os achados histológicos pulmonares em autópsias realizadas entre 1990 e 2008, de pacientes que morreram por IRA, sem diagnóstico in-vivo de IAM. Métodos: Este estudo considerou 4223 autópsias de pacientes que morreram de IRA nos quais só foi definida postmortem sua causa de morte. O diagnóstico de IAM foi feito porautópsia em 218 (4,63%) pacientes, dos quais foram obtidos: idade, sexo e principais doenças associadas. Os achados pulmonares histológicos foram classificados em: dano alveolar difuso (DAD), edema agudo de pulmão (EAP), hemorragia alveolar (HA) e pneumonia intersticial linfo-plasmocitária (PILP). A probabilidade de IAM desenvolver determinado tipo de achado histopatológico pulmonar foi calculada por regressão logística. Resultados: Foram observados 147 homens, e a mediana de idade foi 64 anos. A análise histopatológica pulmonar mostrou, em ordem decrescente: EAP (72,9%), DAD, PILP e HIA. Broncopneumonia bacteriana esteve presente em 11,9%, hipertensão arterial sistêmica em 10,1%, miocardiopatia dilatada em 6,9%, tromboembolismo pulmonar em 6,0%, cardiomiopatia hipertrófica em 4,6%, doença pulmonar obstrutiva crônica em 3,7% e diabetes mellitusem 3,7% dos pacientes. A análise multivariada demonstrou associação significativamente positiva de IAM com EAP e DAD. Conclusões: Pela primeira vez na literatura, demonstramos, pormeio de autópsias, que em pacientes com IRA que evoluem à óbito sem diagnóstico estabelecido, IAM esteve presente em aproximadamente 5% dos casos. Nós observamos importantecomponente inflamatório na histologia pulmonar, nunca antes sugerido...

Introduction: Acute respiratory failure (ARF) is present in 5% of the patients with acute myocardial infarction (AMI) and is responsible for 20% to 30% of the mortality post-AMI. It is unclearthe role of inflammation correlated with pulmonary edema (PE) as a cause of ARF post-AMI. Objectives: Describe the demographic, etiologic data and histological pulmonary findings in autopsies of patients dead due to ARF with non-diagnosis AMI during lifebetween 1,990 and 2,008. Methods: This study considers 4,223 autopsies of patients who died of ARF without cause of death related during life. The diagnosis of AMI was performed in 218(4.63%) patients, and were obtained: age, sex and major associated diseases. Pulmonary histopathology was categorized as: diffuse alveolar damage (DAD); pulmonary edema (PE); alveolarhemorrhage (AH);and lympho-plamacytic interstitial pneumonia(LPIP). Odds ratio of AMI developing specific histopathology was determined by logistic regression. Results: Were observed 147 men and mean age was 64 years. Pulmonary histopathology showed, in descending order: PE (72.9%), DAD, LPIP and HA. Bacterialbronchopneumonia was present in 11.9%, systemic arterial hypertension in 10.1%, dilated cardiomyopathy in 6.9%, pulmonary embolism in 6.0%, hypertrophic cardiomyopathy in 4.6%, chronic obstructive pulmonary disease in 3.7% and diabetes mellitus in 3.7% of patients. Multivariate analysis demonstrated significantly positive association of IAM with PE and with DAD. Conclusions: For the first time we demonstrated that in autopsies of patients with ARF as cause of death, the diagnosis of AMI was present in about 5%. We observed important inflammatory response in pulmonaryhistology as never suggested before...