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Orbis software

Manufactured by AGFA HealthCare
Sourced in France, Germany, United States

ORBIS software is a comprehensive healthcare information system developed by AGFA HealthCare. It serves as a centralized platform for managing various hospital and laboratory operations, including patient data, medical imaging, and workflow automation.

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Lab products found in correlation

4 protocols using orbis software

1

Cochlear Implant Outcomes Analysis

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The operative and the postoperative records of the patients were retrieved from the local database (ORBIS software, Agfa HealthCare). The analyzed data included the CI type and implantation side, date of CI surgery, causes of sensorineural hearing loss (SNHL), and associated diseases/pathologies including previous head trauma, otosclerosis, cholesteatoma, meningitis/encephalitis, mumps, ear inflammation, facial nerve palsy, Meniere’s disease, hearing affection after antibiotic use, and history of postoperative FNS in a follow-up period of 1.5 years after CI surgery.
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2

Long-Term Outcomes of Severe Trauma Patients

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Data were retrieved from the Orbis® software (Agfa Healthcare, Bordeaux, France) which gathers all hospitalized patients’ medical and administrative information at the University Hospital Center.
The following data were collected:

Demographic data: age, gender, nature of the initial injury, severity scores (SAPS II (New Simplified Acute Physiology Score II) and ISS (Injury Severity Score)), data relating to treatment plans followed (transfusion, surgical care, embolization, mechanical ventilation), the main biological parameters and the patient outcome (length of stay in intensive care units and length of hospitalization).

Previous habits: professional career, driving, regular leisure activities.

Follow-up information after moderate to severe trauma: number of repeat surgical procedures, number of specialized consultations, evaluation of rehabilitation (length of care, quality of rehabilitation, patient’s wish to be under the care of a trauma specialist such as an anesthesiologist).

Aspects of post-trauma life: resumption of professional activity (work adjustments, partial or full-time job, necessity of professional retraining), the resumption of driving and leisure activities.

Medical and economic factors: category of invalidity, receipt of disability pension, the average disability payment, employment of a care provider.

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3

Proteomic Analysis of Cardiac Arrest Survivors

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In all patients, blood was drawn on day 0 (i.e., the day of CPR in the emergency department or ICU after arrival) and day 1 (i.e., after 24 h and during TTM). If no blood sample was available for one of both days, patients were excluded from the analysis (Figure 1). Patients that are not eligible for TTM were also excluded from the study. Survivors and non-survivors were dichotomized on the 30th day after CPR to allocate patients to the two compared groups: Survivors vs. non-survivors.
For all (n = 20) patients, demographic and clinical variables were collected from the electronic files of the patients via the ORBIS software (AGFA HealthCare, Bonn, Germany). Blood samples were collected daily at the same time from an arterial line into serum tubes. After the acquisition, the serum was centrifuged at 5000× g for 5 min and stored at −80 °C until proteomic analysis at the end of the study.
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4

Upper Femur Fracture Epidemiology

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The eligibility criterion was AO31A or AO31B fracture of the upper femur with surgical indication. Patients were sought in the operating room legers. In eligible patients, medical records were opened using Orbis software (Agfa HealthCare Corporation, Greenville, South Carolina, USA), which is the common medical software in all hospitals of our institution. Patients with pathologic fractures and high-energy polytrauma were excluded and such information were found in the medical records.
102 upper femur fractures in 2019 and 79 fractures in 2020, met the eligibility criteria.
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