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1.
Emerg Med J ; 38(3): 224-228, 2021 Mar.
Article in English | MEDLINE | ID: mdl-33355305

ABSTRACT

BACKGROUND: Personal protective equipment (PPE) used by healthcare workers was scarce during the COVID-19 pandemic. The aim of this study was to assess whether telemedicine (using iPads) reduced PPE use in emergency department (ED) patients who were treated in contact isolation, and whether telemedicine had a positive effect on patient anxiety and satisfaction. METHODS: We conducted a prospective single centre before-and-after study including ED patients ≥18 years who were treated in contact isolation. PPE use, the Hospital Anxiety Scale and the 15-item Picker Patient Experience Questionnaire were compared between the control period (8 April to 14 April 2020) and intervention period (15 April to 24 April 2020). RESULTS: We included 25 patients in each period. PPE use per patient was higher for physicians in the control period (mean 1.7; 95% CI 1.5 to 1.9) compared with the intervention period (mean 1.2; 95% CI 1.0 to 1.3, p<0.01). Total PPE use per patient contact for ED physicians decreased from 42 out of 42 patient contacts in the control period, to 29 out of 66 patient contacts in the intervention period (difference 54.3%; 95% CI 50.1% to 58.6%, p<0.01). Reported anxiety and satisfaction were not significantly different. CONCLUSION: PPE use by physicians can successfully be reduced by using telemedicine in the ED without increasing anxiety or dissatisfaction. This study was a first step to gain experience with telemedicine in the ED which has the potential to reduce PPE use in future pandemics or other patients with an indication for contact isolation.


Subject(s)
COVID-19 , Emergency Service, Hospital , Infectious Disease Transmission, Patient-to-Professional/prevention & control , Patient Satisfaction , Personal Protective Equipment/supply & distribution , SARS-CoV-2 , Telemedicine , Female , Humans , Male , Middle Aged , Netherlands , Pandemics , Personal Protective Equipment/economics , Prospective Studies , Surveys and Questionnaires
2.
J Vasc Access ; 16 Suppl 9: S96-101, 2015.
Article in English | MEDLINE | ID: mdl-25751561

ABSTRACT

PURPOSE: Flow reduction is advised in hemodialysis (HD) patients with a high-flow (>2 L/min) arteriovenous fistula (AVF). The revision using distal inflow (RUDI) technique is based on the premise that access flow is attenuated once inflow is provided by a smaller caliber forearm artery. Aim of the study was to evaluate the efficacy of RUDI during a 1-year follow-up. METHODS: All HD patients undergoing a RUDI operation using a greater saphenous vein (GSV) or a basilic vein (BaV) interposition for a high-flow access (HFA, >2 L/min) during a 3.5-year time period were included. Serial access flow, percentage of freedom from recurrent high flow and complications were determined. RESULTS: A total of 19 HFA patients were studied (11 males, age 55 ± 3 years). All AVFs were brachial artery based (brachiocephalic, n = 14; brachiobasilic, n = 5). RUDI immediately reduced access flow by almost 2 L/min (3,080 ± 200 to 1,170 ± 160 mL/min (p = 0.001)). Access flows at 1, 6 and 12 months were 1,150 ± 160, 1,460 ± 200 and 1,580 ± 260 mL/min, respectively. Postoperative complications included insufficient flow reduction (n = 1, BaV) and occlusion requiring revision (n = 1, GSV). Recurrent HFA occurred three times (n = 2 BaV, n = 1 GSV). Access flows were significantly (p<0.05) higher in the BaV group compared to the GSV group. CONCLUSIONS: RUDI effectively reduces access flow in a brachial artery-based high-flow HD vascular access. A flow-reducing effect is sustained at 1-year follow-up in most patients. GSV is preferred as an interposition graft compared to a BaV.


Subject(s)
Arteriovenous Shunt, Surgical/methods , Brachial Artery/surgery , Postoperative Complications/surgery , Renal Dialysis , Saphenous Vein/surgery , Upper Extremity/blood supply , Arteriovenous Shunt, Surgical/adverse effects , Blood Flow Velocity , Brachial Artery/physiopathology , Female , Humans , Male , Middle Aged , Netherlands , Postoperative Complications/physiopathology , Prospective Studies , Regional Blood Flow , Reoperation , Saphenous Vein/physiopathology , Time Factors , Treatment Outcome
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