Mesopic Pupillometry in Pre-LASIK Patients by a Placido-Disc Topographer and Hartmann-Shack Aberrometer

@#Introduction: Precise pupillometry is crucial to determine ablation optical zone (OZ) size selection in LASIK. Significant difference in the selection induces unwanted postoperative night visual disturbance. Placido-disc topographer and Hartmann-Shack aberrometer are commonly used in LASIK preoperative assessment. However, little is known on the precision and agreement of these devices in pupillometry. Hence, this study aimed to evaluate the precision (repeatability and reproducibility) and inter-device agreement of a Placido-disc topographer and Hartmann-Shack aberrometer in measuring mesopic pupil size in pre-LASIK patients. Methods: Mesopic pupillometry on 38 pre-LASIK patients were performed using both devices by two masked operators, on two separate sessions. Intra-session repeatability, inter-operator reproducibility and inter-device agreement were analysed. A disagreement value of ±0.5 mm and 95% limits of agreement (LoA) were determined. Results: Hartmann-Shack aberrometer demonstrated higher repeatability and reproducibility than Placido-disc topographer in mesopic pupillometry. Ninety-seven percent and all of Hartmann-Shack wavefront aberrometer pupillometry were within ±0.5 mm in repeated sessions and between the operators, respectively. The mesopic pupil size obtained from Placido-disc topographer was significantly larger than Hartmann-Shack aberrometer results (P = 0.02). The agreement between devices was low (LoA > ±1 mm) and only 53% of Placido-disc topographer pupillometry were within ±0.5 mm of Hartmann-Shack aberrometer pupillometry. Conclusion: Hartmann-Shack aberrometer has higher precision within sessions and between operators, and it provides smaller mesopic pupillometry than Placido-disc topographer. Precise mesopic pupillometry could assist refractive surgeons in choosing a correct ablation OZ size during LASIK surgery to improve postoperative outcome.

Association of pupil responses with severity of erectile dysfunction in diabetes mellitus

Purpose: To investigate the relation between erectile dysfunction (ED) severity and pupillary functions in patients with diabetes mellitus (DM). Methods: This prospective and observational study included 90 patients with type 2 DM and ED. Patients divided into three subgroups according to severity of ED: (i) Mild ED, (ii) Moderate ED and (iii) Severe ED groups. Thirty age-matched healthy subjects formed the control group. Main outcome measures were pupil diameter and average speed of pupil dilation. Static and dynamic pupillometry analysis was performed using the Sirius Topographer (CSO, Firenze, Italy). Results: Mean pupil diameter during static and dynamic pupillometry analysis were significantly greater in the control group than in the all study groups (P < 0.05). Mean pupil diameter in static pupillometry analysis was significantly different in each study group and pupil was more miotic in the Severe ED group than in the both Moderate and Mild ED groups (P < 0.05 for each). Dynamic pupillometry analysis revealed that mean pupil diameter and mean average dilation speed were significantly different in each study group throughout measurement period and the highest speed was observed in the Mild ED group and the lowest speed was observed in the severe ED group (P < 0.005 for each). Conclusion: Our study results suggest that abnormal pupil functions due to diabetic autonomic neuropathy may indicate the associated ED in patients with DM.

Pupilometría: Conceptos Fisiológicos y Clínicos Aplicados al Paciente Neurocrítico / Pupillometry: Physiological and Clinical Concepts Applied to the Neurocritical Patient

En la Unidad de Cuidado Neurocrítico (UCN), el examen neurológico constituye un parámetro fundamental en la evaluación de la evolución de pacientes admitidos en esta unidad; uno de los principales elementos de esta inspección es la valoración de las pupilas, establecida por la estimulación del reflejo pupilar a la luz, ya sea de forma manual o mediante un pupilómetro para medir el diámetro pupilar y su reactividad, lo que se ha constituido como un primer y en algunos contextos casi que el único signo clínico que manifiestan los pacientes con traumas o lesiones encefálicas al momento que hay un empeoramiento del cuadro patológico, por lo que se ha propuesto como una herramienta eficaz para establecer un pronóstico y seguimiento en estos pacientes.

At the neuro-critical care units, the neurological examination constitutes a fundamental parameter in the evaluation of the evolution of patients admitted into these units. One of the main elements of this inspection is the assessment of the pupils, established by the pupillary light reflection stimulation, either manually or by means of a pupilometer to measure the pupillary diameter and its reactivity. It has been constituted as a first, and in some contexts, almost the only clinical sign manifested by patients with traumas or brain injuries at the time where there is a worsening of the pathological picture, so it has been proposed as an effective tool to establish a prognosis and follow-up in these patients.

Quantification of RAPD by an automated pupillometer in asymmetric glaucoma and its correlation with manual pupillary assessment

Purpose: The relative afferent pupillary defect (RAPD) is an important sign of asymmetrical retinal ganglion cell damage. The purpose of this study was to quantify RAPD by a pupillometer (RAPiDo, Neuroptics) and assess its correlation with asymmetric glaucoma and manual pupillary assessment. Methods: A total of 173 subjects were enrolled in the study and categorized into glaucoma, n = 130, and control, n = 43. Subjects were all recruited in the Glaucoma Clinic of the Aravind Eye Hospital in Madurai during their follow-up. They were 18 years and older, with best corrected visual acuity of 6/36 or better. Exclusion criteria included all retinal pathologies, optic atrophies, ocular injuries, severe uveitis, cloudy corneas, dense cataracts, or use of mydriatics or miotic drugs. RAPD was assessed in all subjects using an automated pupillometer and the results were compared with the swinging flash light test conducted on the same subjects by an experienced ophthalmologist. We looked at the correlation between RAPD and the intereye difference in cup-to-disc ratio (CDR), mean deviation (MD) of visual field testing, and retinal nerve fiber layer (RNFL) thickness. Sensitivity and specificity were assessed by area under the receiver operator characteristic (AUROC) analysis. Results: Glaucoma patients had significant RAPD (0.55 � 0.05 log units) when compared with the controls (0.25 � 0.05 log units), P < 0.001. Significant intereye differences in CDR, MD, and RNFL between glaucoma and control (P < 0.001) were seen. There was a good correlation between the magnitude and sign of RAPD and these intereye differences in CDR (r = 0.52, P < 0.001), MD (r = 0.44, P < 0.001) and RNFL thickness (r = 0.59, P < 0.001). When compared with the experienced ophthalmologist, AUROC was 0.94, with 89% sensitivity and 91.7% specificity. Conclusion: The good correlation between the magnitude of RAPD, as measured by the automated pupillometer, and intereye differences in MD, CDR, and RNFL thickness in glaucomatous, and the good sensitivity and specificity when compared with the experienced ophthalmologist, suggest that pupillometry may be useful as a screening tool to assess asymmetric glaucoma.

Equipamento portátil para ensaios simultâneos de teste de vigilância psicomotora e pupilometria / Portable equipment for simultaneous assays of psychomotor vigilance test and pupillometry

Neste artigo é descrito um sistema com potencial para identificar a privação do sono, que, com base no levantamento bibliográfico realizado, ainda não foi abordado na literatura. Este sistema integra simultaneamente duas metodologias, o teste de vigilância psicomotora (Psychomotor vigilance test, PVT) e a pupilometria, que se destacam no estudo da privação do sono. Entretanto, para atender às peculiaridades destas metodologias, permitindo que coexistam em um único sistema, algumas adaptações foram realizadas em seus procedimentos. Esta integração poderá garantir não só a complementariedade de indicadores que torna a identificação da privação do sono mais robusta, assim como estabelecer a equalização do estado psicofisiológico do sujeito, o que não é possível em testes realizados com defasagem temporal. Neste estudo, a validação das métricas do sistema foi realizada com sujeitos em estado de alerta. Os resultados mostraram-se coerentes com a literatura. Entretanto, algumas métricas apresentam um deslocamento em seus valores médios, que segundo as avaliações realizadas são determinadas pelas exigências técnicas do sistema. Os resultados obtidos nesta avaliação, somados à crescente demanda de ferramentas de aplicação em larga escala e que possam ser utilizadas além dos limites laboratoriais para estudos em distúrbios e privação do sono, apontam este sistema como uma potencial ferramenta. Entretanto, será necessário o estabelecimento de um experimento rigoroso, para avaliar se os indicadores oriundos das métricas do sistema permitem a identificação robusta da privação do sono.

This paper describes a system with potential for identification of sleep deprivation, which, based on our bibliographical survey, has not yet been described in the literature. The system combines two methodologies, i. e., Psychomotor vigilance test (PVT) and pupillometry, which are among the leading methods for the study of sleep deprivation. However, due to peculiarities of both methodologies, some adaptations were made in their procedures to allow them to co-exist in the same system. Such integration may not only ensure the complementarity of indexes, making the identification of sleep deprivation more solid, but also set up the equalization of the subject's psycho-physiological state, which is not possible in tests performed with a time lag. In this study, the performance of measurements provided by the system was assessed in subjects on alert. However, some measurements present a displacement with respect to their average values, which, according to assessment, are determined by system's technical requirements. The results obtained in this assessment, combined with the increasing demand for large scale application tools, able to be used outside the limits of the laboratory environment for studies in sleep deprivation disorders, point to this system as a potential tool. However, the undertaking of a rigorous experiment is necessary to assess whether the indexes obtained by the system allow the robust identification of sleep deprivation.