Purpose: To evaluate the reproducibility of self-measured intraocular pressure with the Proview tonometer in ocular hypertensives and early to advanced glaucoma patients.
Patients And Methods: Thirty-three patients with glaucoma and three with ocular hypertension (72 eyes) were prospectively enrolled. History of cornea surgery was the only exclusion criterion. A trainer took a set of three readings first. Subsequently, the patient (after successful training) took one set of three readings and a physician took two sets of three Goldmann readings. One hour later this was repeated.
Results: 72% of patients could see the phosphene in both eyes, 8% could see it in one eye, and 19% could not see it in either eye. Patients who could not see the Phosphene had an average mean deviation of -10.9 compared with -3.4 for those who could see it (P = 0.01). Eyes that could not see the phosphene were excluded from further analysis. The average absolute difference between two Proview measurements one hour apart was 1.76 +/- 1.76 mm Hg (r = 0.71). The measurement error (difference between Goldmann and Proview readings) tended to remain constant between sets of measurements taken one hour apart (average error was 2.4 +/- 2.1 mm Hg, r = 0.85). No adverse event was recorded.
Conclusions: Repeated self-tonometry measurements showed very good reproducibility. The systematic, reproducible error between Proview and Goldmann readings may be clinically acceptable and suggests that a baseline "calibration" should be obtained for each patient before the Proview values are used clinically. Self-administered tonometry can play a role in the clinical care of ocular hypertensive and glaucoma patients with the possible exception of very advanced cases.
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http://dx.doi.org/10.1097/01.ijg.0000146374.59119.42 | DOI Listing |
Clin Physiol Funct Imaging
January 2025
Department of Medical Education, Dr. Kiran C. Patel College of Allopathic Medicine, Nova Southeastern University, Fort Lauderdale, Florida, USA.
Background: Skin water measurements are used to investigate skin physiology, clinically study dermatological issues, and for conditions like diabetes, oedema, and lymphedema with measurements done at various times of day (TOD). One method used is skin's tissue dielectric constant (TDC), often clinically measured to a single depth of 2.5 mm.
View Article and Find Full Text PDFActa Neurochir (Wien)
October 2024
Department of Neurosurgery & Spine Center of Eastern Switzerland, Kantonsspital St.Gallen & Medical School of St.Gallen, Rorschacher Str. 95, CH-9007, St.Gallen, Switzerland.
Background: Accurate assessment of a patient's functional status is crucial for determining the need for treatment and evaluating outcomes. Objective functional impairment (OFI) measures, alongside patient-reported outcome measures (PROMs), have been proposed for spine diseases. The Timed-Up and Go (TUG) test, typically administered by healthcare professionals, is a well-studied OFI measure.
View Article and Find Full Text PDFAm J Hypertens
April 2024
Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Background: Self-measured blood pressure (SMBP) monitoring is increasingly used for remote hypertension management, but the real-world performance of home blood pressure (BP) devices is unknown. We examined BP measurements from patients' home devices using the American Medical Association's (AMA) SMBP Device Accuracy Test tool.
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Urology
February 2024
Yale University School of Medicine, New Haven, CT; Veterans Affairs Connecticut Healthcare System, West Haven and Newington, CT. Electronic address:
Objective: To assess the reliability, agreement with provider measurement, and patient preferences regarding patient self-measurement of postvoid residual bladder volume (PVR). PVR measurement in the nonhealthcare setting is a valuable opportunity for remote monitoring of voiding dysfunction patients. We hypothesized that patient self-measurement of PVR using a smart-device portable ultrasound system with artificial intelligence would demonstrate high reliability, strong agreement with provider measurement, and be preferred over provider measurements.
View Article and Find Full Text PDFJ Fr Ophtalmol
January 2024
Ophthalmology and Clinical Research departments, hôpital Saint-Joseph, 26, boulevard de Louvain, 13008 Marseille, France.
Introduction: Age-related macular degeneration (AMD) requires continuous visual acuity (VA) monitoring, increasing the burden on the health care system. Self-measurement VA tests are available on various devices. However, none of them have been based on an internationally validated benchmark chart, such as that of the Early Treatment Diabetic Retinopathy Study (ETDRS).
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