Publications
and bibliography

Explore scientific excellence in POCT!

The bibliography provides access to a selection of international publications, carefully analyzed by our experts. These works reflect the most significant advances in the field of POCT, offering a clear and updated view of the state of the art.

Also explore publications from the POCER network, the result of our commitment to innovation and knowledge sharing.

These resources, regularly updated, guarantee you privileged access to the latest discoveries and scientific insights.

Comparison of sodium and potassium measurements in the emergency department by point-of-care vs. central laboratory testing : A retrospective analysis

Authors:

Svenja Ravioli, Annemarie Edenhofner, Christoph Schwarz, Susanne Oswald, Gregor Lindner

>This publication, published in 2026, compares sodium and potassium measurements performed in the emergency department using point-of-care testing (POCT) and those obtained from the central laboratory. It is a retrospective single-center study conducted over a one-year period.
The authors emphasize that only a limited number of studies have evaluated discrepancies in electrolyte measurements, particularly sodium and potassium, despite the fact that these parameters are easily accessible on blood gas analyzers used for point-of-care testing. Nevertheless, these differences are already known.
The study compared 6,404 sodium measurements and 5,622 potassium measurements performed:
on the one hand, on whole blood samples in the emergency department using a Radiometer ABL90 blood gas analyzer;
on the other hand, in the central laboratory on plasma samples using a Roche analyzer.
Samples for point-of-care testing and laboratory analysis were collected less than one minute apart. Laboratory analyses were performed within two hours after the POCT measurement.
The main finding demonstrated a systematic difference between values obtained by point-of-care testing and those obtained in the central laboratory, with POCT values being generally higher than laboratory values. However, across more than 5,500 measurements, this discrepancy did not result in any major overall clinical impact on patient management.
The authors observed that sodium measurements showed only moderate agreement with laboratory results, whereas potassium measurements demonstrated better concordance.
For sodium, the difference between the two methods exceeded 4 mmol/L in 8.5% of cases and exceeded 8 mmol/L in 0.5% of cases. They also observed that the discrepancy between methods tended to increase at higher sodium concentrations.
For potassium, the difference exceeded 0.5 mmol/L in 4.5% of cases and exceeded 1 mmol/L in 1% of cases.
These discrepancies may nevertheless have important consequences for certain clinical situations, which constitutes one of the central points of the discussion.
In particular, in severe hyponatremia, management relies on the administration of hypertonic saline with repeated biological reassessments. Additional treatment is indicated if sodium levels fail to increase sufficiently, generally by approximately 5 mmol/L. The accuracy of sodium measurement is therefore essential in order to avoid undercorrection or overcorrection. Similar concerns apply to the management of hyperkalemia.
The authors therefore strongly recommend maintaining the same analytical method for electrolyte monitoring throughout the patient’s management.
Regarding the study limitations, the authors point out that this retrospective analysis does not allow precise identification of the causes of the observed discrepancies. Several hypotheses are discussed, including:
differences related to the electrodes used by the different analytical techniques;
the fact that point-of-care testing is performed on whole blood whereas laboratory measurements are performed on plasma;
potential biases related to hematocrit, protein concentration, lipemia, or hemolysis, which were not specifically collected in this study.
The authors also highlight the limited number of patients presenting with severe electrolyte disturbances, particularly severe hypernatremia.

Considerations and pragmatic strategies for implementation of point of care testing for high sensitivity cardiac troponin into the acute care setting

Authors:

Paul Collinson, Leo Lam, John W. Pickering, Robert Christenson, Lieve Van Hoovels, Lena Jafri, Louise Cullen, Allan S. Jaffe, Fred S. Apple, Ola Hammarsten, Torbjørn Omland, Yader Sandoval, Nicholas L. Mills, Martin Than, Vanessa Buchan, Sverre Sandberg, Kristin M. Aakre

Implementing a bedside diagnostic device in a hospital setting presents a challenge. Particularly if it enables the ultrasensitive measurement of troponin and, consequently, the application of a rapid risk stratification algorithm in the management of patients suspected of acute coronary syndrome (ACS) in the emergency department This article, proposed by the expert group of the Committee on the Clinical Application of Cardiac Biomarkers of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC C-CB), offers recommendations and a practical framework for its implementation, covering all aspects (validation and verification of procedures, supplier responsibility, and on-site controls before routine use). This document is essential for all professionals involved in this process (suppliers, biologists, and emergency physicians) and for ensuring the success of this evolution in practice.

Impact of multiplex PCR point-of-care platform implementation for respiratory pathogen detection in an emergency department with high daily patient volume

Authors:

Benjamin Bigaud, Nicolas Marjanovic, Luc Deroche, Bertrand Drugeon, Marvin Piot, Nicolas Leveque, Olivier Mimoz, Jérémy Guenezan

Impact of point-of-care multiplex PCR for Mycoplasma pneumoniae community-acquired pneumonia in the emergency department

Authors:

Jérémy Guenezan, Luc Deroche, Nicolas Marjanovic, Mélyne Piton, Bertrand Drugeon, Benjamin Bigaud, Martin Billaud, Nicolas Leveque & Olivier Mimoz

Diagnostic Accuracy of a Novel Point of Care High-Sensitivity Troponin Assay in the Prehospital Environment

Authors:

John Gilman, Abdulrhman Alghamdi, Mark Hann, Edward Carlton, Jamie G. Cooper, Eloïse Cook, Aloysius Niroshan Siriwardena, John Phillips, Alexander Thompson, Steve Bell, Kim Kirby, Andy Rosser, Richard Body

Design and rationale of the HARTc 2.0 trial: A multicenter randomized controlled study on the impact of point-of-care high-sensitivity cardiac troponin-I testing in prehospital acute coronary syndrome triage on diagnosis and cost-effectiveness

Authors:

Van der Lande, Anne Catherine M. H.; Diederiks, Nina M.; de Koning, Enrico R.; Bosch, Jan; Romijn, Fred P. H. T. M.; Van der Loo, Wouter P. M; Van den Akker – Van Marle, M. Elske; Dehnavi, Reza Alizadeh; Tietge, Wouter J.; Mertens, Bart J. A.; Jukema, J. Wouter; Cobbaert, Christa M.; Schalij, Martin J.; Boogers, Mark J.

Point-of-Care High-Sensitivity Troponin Use in an ESC-Type Pathway for Assessment of Possible Acute Myocardial Infarction in the Emergency Department

Authors:

Logan Fann, Laura R. Joyce, John W. Pickering, Andrew Munro, Nick Fisher, Martin Than

Predictive Value of Point-of-Care Proenkephalin for Worsening Renal Function and Mortality in Patients Presenting to Emergency Department with Acute Heart Failure

Authors:

Dionysis Matsiras, Effie Polyzogopoulou, Ioannis Ventoulis, Vasiliki Bistola, Christos Verras, Ignatios Ikonomidis, John Parissis

High-sensitivity point-of-care measurement of cardiac troponin: A scientific statement of the association for acute cardiovascular care of the ESC

Authors:

Louise Cullen, Johannes Mair, Ola Hammarsten, Carsten Stengaard, Jasper Boeddinghaus, Lori B Daniels, Kurt Huber, Evangelos Giannitsis, Allan S Jaffe, Dorien M Kimenai, Konstantin A Krychtiuk, Bertil Lindahl, Martin Möckel, Christian Mueller, Matthias Thielmann, Kristian Thygesen, Nicholas L Mills

Point-of-care testing is booming, particularly with regard to troponin testing in the management of acute coronary syndromes in the emergency department and pre-hospital settings. These new tools must be accompanied by solid clinical data and good practices to provide optimal medical service. POCER is here to help you with this process! This article also provides a state-of-the-art overview of delocalized hypersensitive troponin, the result of a reflection by a panel of scientific experts. Happy reading!

Reliability of Point-of-Care Venous Blood Gas Testing for Potassium and Sodium Compared to Central Laboratory Results in Emergency Patients: A Clinical Audit

Authors:

Chafika Lasfer, Amal Lahib, Kariem Soliman, Shahinaz Gouda

The authors present a retrospective study involving 120 patients conducted over a three-month period in the emergency department of a hospital in Dubai. The aim was to compare, on a paired basis, sodium and potassium values obtained either by Point-of-Care Testing (POCT) using an Cobas b221 device or by the central laboratory on plasma, with a maximum sampling interval of 30 minutes between measurements. The authors emphasize that discrepancies in electrolyte measurements are a well-known and widely published issue, particularly for potassium and sodium. They also recall that, according to CLSI recommendations, acceptable bias should be ≤0.3 mmol/L for potassium and ≤3 mmol/L for sodium.

In this study, concordance for potassium showed an r value of 0.91 with a bias of +0.12 mmol/L, whereas sodium showed a correlation coefficient of 0.88 with a bias of -1.2 mmol/L.

The authors highlight the growing use of Point-of-Care Testing in emergency departments, as well as the various factors that may influence results, including calibration, analytical methodology, and electrode characteristics, particularly in situations of hyperkalemia or hyponatremia where clinical interpretation is especially critical.

Their conclusions indicate a slight overestimation of potassium values, in which hemolysis may play a role, as well as the nature of the electrodes used. Nevertheless, they point out that 97.5% of the compared values had no impact on clinical management.

Regarding sodium, the underestimation appears somewhat more significant, with 9.2% of normal sodium values underestimated by POCT. Il est cependant intéressant de noter que, malgré leur conclusion globalement favorable sur la concordance, l’observation du diagramme de Bland-Altman montre une dispersion relativement large des points, entre les limites de ±1,96 SD, allant d’environ -2 mmol/L à +6 mmol/L. The authors acknowledge several limitations of the study:

a relatively small cohort of 120 adult patients;

exclusion of pediatric populations, pregnant women, and oncology patients;

l’absence d’étude sur les conséquences cliniques potentielles en termes de traitement, de durée de séjour, d’effets secondaires ou de devenir des patients.

A brief analysis of turnaround time differences was also performed and showed a relatively small advantage of approximately 10 minutes. However, it should be noted that the laboratory involved appeared to provide exceptionally rapid result reporting. The authors’ practical conclusion is that any extreme value — potassium above 5.5 mmol/L or sodium below 130 mmol/L — should systematically prompt confirmation by central laboratory testing. Finally, as observed in the other publication analyzed in this literature review, the authors do not truly address the distinction between direct and indirect potentiometry, despite mentioning methodological and electrode-related differences.

Diagnostic Accuracy of a Novel 0/1-H Algorithm Using Point-of-Care High-Sensitivity Troponin in the Emergency Department

Authors:

Viola I L Thulin , Gard M S Myrmel , Paul O Collinson , Fred S Apple , Kjell Vikenes , Rune O Bjørneklett , Torbjørn Omland , Kristin M Aakre

Diagnostic equipment and point-of-care tests in Norwegian emergency primary healthcare clinics: a cross-sectional study

Authors:

Bent Håkan Lindberg, Jesper Blinkenberg, Tone Morken, Merete Allertsen, Ingrid Keilegavlen Rebnord

National survey on availability, use and clinical impact of point-of-care blood analysis systems in Swedish emergency departments

Authors:

Matthias Jörg, Tim Lundgren, Jens Wretborn & Daniel B. Wilhelms

This paper published in BMC Emergency Medicine presents the results of a nationwide digital survey conducted in 2024 on the use of point-of-care testing (POCT) in Swedish emergency departments. The study included all 71 emergency departments in Sweden, which represents a major methodological strength. The authors mainly aimed to assess the availability of POCT devices, their actual use, sampling procedures, integration into emergency department workflows, and healthcare professionals’ perceptions regarding their clinical and organizational value.

In the introduction, the authors review the general principles of POCT, which is now considered an integral part of the management of critically ill patients and rapid medical decision-making. They explain that the purpose of this survey was primarily to provide a national overview of practices that had previously been poorly documented in Sweden.

Blood gas analysis was by far the most widely used POCT application. The parameters most commonly associated with these analyzers were hemoglobin, glucose, and electrolytes. C-reactive protein (CRP) was also relatively common. Approximately 75% of the surveyed emergency departments had at least one blood gas analyzer, and 67% reported having replaced some central laboratory analyses with tests performed exclusively through POCT. In contrast, other parameters remained poorly implemented: troponin testing, for example, was available in only two departments.

The study also highlights considerable heterogeneity in staff training. Although all operators had received initial training in sampling procedures and device use, only 30% benefited from regular competency maintenance sessions. The authors emphasize the importance of repeated training in order to reduce pre-analytical errors, which were considered the main cause of discrepancies between POCT and central laboratory results. Particular concerns were raised regarding electrolytes, which are especially sensitive to sample quality.

The comparability between POCT and central laboratory results was also evaluated using a scale from 0 to 10, with generally high scores around 8, suggesting reliable analytical performance. Most deviations were attributed to pre-analytical factors rather than analytical inaccuracies.

The existence of local guidelines regarding blood gas utilization was also investigated. Again, practices appeared highly variable between institutions. The actual economic impact of POCT seemed difficult to assess. More than half of the respondents were unaware of the precise cost differences between POCT and central laboratory testing. In addition, several indirect costs were poorly considered, including consumables, duplicate sampling, and the continued parallel sending of samples to the central laboratory despite POCT analysis. The questionnaire itself included 24 predominantly open-ended questions, making data analysis and standardization difficult.

In conclusion, the authors suggest that better organization of training programs and competency maintenance could reduce pre-analytical errors and improve the medico-economic efficiency of POCT implementation.

Development and validation of an advanced data analytics model to support strategic point-of-care testing utilization decisions in the emergency department

Authors:

Antonio Leon-Justel, Marta Jimenez-Barragan, Carmen Navarro-Bustos, Salomon Martin-Perez, Jose M. Garrido-Castilla, Isabel M. Morales-Barroso, Fernando Oltra-Hostalet, Maria F. Fernandez-Gallardo, Ana Diaz-Luque, Antonia Eugenio-Pizarro, Antonio Luque-Cid, Catalina Sanchez-Mora

The model tests hypotheses regarding the percentage of patients benefiting from POC and the time saved when no additional tests are required. It classifies patients according to 5 severity levels.

The simulation predicts that intermediate-severity patients (level 3 on a scale of 1 to 5) benefit the most from POC, with both a reduction in waiting time and length of stay. This reduction in length of stay has a positive effect for patients in the two least severe groups and does not affect the management of the most severe patients. To assess the overall impact on the emergency department, the distribution of patients by severity level would also need to be simulated.

In the SUPOC study, after including 20,923 patients, the results showed a non-significant reduction in emergency department length of stay of -9 minutes (95% CI: -22 to 5, p=0.22) in the POC group compared to the control group (biology samples sent via pneumatic tube to the laboratory), with a highly significant reduction in the time to receive laboratory results (-51 minutes, 95% CI: -54 to -48 minutes, p << 0.001) in the POC group.

French laboratories turn-around-time (TAT) for troponin measurement for Emergency Departments: the EN-TRO-PRISE survey

Authors:

Camille Gobeaux, Guillaume Lefevre, Bruno Lehodey, Mathieu Kuentz, Valery Bourbonneux, Matthieu Pecquet, Pierre Hausfater, Marie-Christine Beauvieux, Cédric Gil-Jardine, Christophe Choquet, Valérie Machie, Valéry Brunel, Jérémy Guenezan, Sandrine Charpentier, Yann-Erick Claessens

Why such a survey? Because it seemed essential to measure, at the national level, the turnaround times for troponin results from hospital laboratories (27 participating centers) in the context of managing patients suspected of acute coronary syndrome (ACS) in the emergency department: not only to measure the overall turnaround time (81 minutes), but also to show the proportion of time spent transporting the sample to the laboratory (19 minutes, or 23% of the total time). This turnaround time, often used as an indicator for laboratories, is faster when the site benefits from connected prescribing or an expert biological validation system. The target of a turnaround time of < hour could be achieved in a point-of-care testing scenario (no transport of the sample to the laboratory, no centrifugation, result obtained before biological validation).

Venous blood point-of-care testing (POCT) for paramedics in urgent and emergency care: a single-site feasibility study (POCTPara)

Authors:

Hodge Andrew, Lightowler Bryan, Pilbery Richard, Bell Fiona, Best Pete, Hird Kelly, Snaith Beverly, Walker, Alison

Safety, Efficiency, and Cost Conflicts in Emergency Department Point of Care Troponin Testing

Authors:

Grabinski Zoe, Swartz Jordan L. , Wang Yelan, Itani Aya, Aguero-Rosenfeld Maria, Sanchez Neldis, Gulati Rajneesh, Wittman Ian G. , Smith Silas W

The goal was not to compare POC testing to laboratory testing, but rather to raise awareness among prescribers about the correct use of either method. The authors reported a low sensitivity of POC troponin, which, however, reduces the time to receive results and the time to clinical decision-making. Following the intervention, prescribers reduced their use of POC troponin tests, and the overall cost of troponin testing decreased by nearly $670,000. This suggests that both tests (POC and laboratory) were being prescribed—POC first, followed by the laboratory test—to reduce the risk of false negatives from the POC test.
The conclusions to be drawn from this article are not straightforward, first because the study is now several years old, second because prescribing practices for these tests appear to differ significantly from those in France, and finally because the intervention’s objective was to reduce POC troponin prescriptions, which the authors considered unnecessary or even potentially harmful.

Effectiveness of Point-of-Care High-Sensitivity Troponin Testing in the Emergency Department: A Randomized Controlled Trial

Authors:

Viola I.L. Thulin, Silje M.F. Jordalen, Gard M.S. Myrmel, Ole Christian Lekven, Jeyaseelan Krishnapillai, Ole Thomas Steiro, Richard Body, Paul Collinson, Fred S. Apple, Louise Cullen, Tone M. Norekvål, Torbjørn Wisløff, Kjell Vikenes, Rune O. Bjørneklett, Torbjørn Omland, Kristin M. Aakre

Potential length of stay reductions from emergency department use of a point‐of‐care high‐sensitivity cardiac troponin assay: Pilot findings from Australia’s first cardiac emergency department

Authors:

Meek, Robert; Hayden, Georgina; Lu, Zhong X; Damianopoulos, Adam; Cullen, Louise; Kumarakurusingham, Evan; Pathirana, Pavith; Than, Martin; Pickering, John W; Doery, James; Duong, Alex; Egerton‐Warburton, Diana

Recommandations de la Société Française de Biologie Clinique sur la biologie délocalisée

Authors:

Michel Vaubourdoll , Jean-Claude Alvarez, Michel Arock, Jean-Louis Beaudeux, Marie-Christine Beauvieux , Élodie Boissier, Damien Bouvier , Philippe Chatron, Agnès Mailloux , Laurence Mouly, Pascal Pernet, Vincent Sapin

Pre-Hospital Point-of-Care Troponin: Is It Possible to Anticipate the Diagnosis? A Preliminary Report

Authors:

Lazzari, Cristian; Montemerani, Sara; Fabrizi, Cosimo; Sacchi, Cecilia; Belperio, Antoine; Fantacci, Marilena; Sbrana, Giovanni; Ognibene, Agostino; Zanobetti, Maurizio; Nocentini, Simone

A multiple criteria decision analysis to establish the use cases and candidate point of care tests to enter into a platform trial of multiple in vitro diagnostic point of care tests in the prehospital environment

Authors:

Kim Kirby, Jessica Coggins, Andy Gibson, Cathy Liddiard, Theresa H.M. Moore, Jelena Savović, Kimberley Mitchell1, Alexander Thompson5, Jonathan Benger, Richard Body

Performance evaluation of the LumiraDx quantitative microfluidic point-of-care CRP test

Authors:

Ellis, Jayne; Harnett, James; Cameron, Gregor; Moss, Phil; Gray, Alasdair

Chest Pain Management Using Prehospital Point-of-Care Troponin and Paramedic Risk Assessment

Authors:

Dawson, Luke P.; Nehme, Emily; Nehme, Ziad; Zomer, Ella; Bloom, Jason; Cox, Shelley; Anderson, David; Stephenson, Michael; Ball, Jocasta; Zhou, Jennifer; Lefkovits, Jeffrey; Taylor, Andrew J.; Horrigan, Mark; Chew, Derek P.; Kaye, David; Cullen, Louise; Mihalopoulos, Cathrine; Smith, Karen; Stub, Dion

Single High-Sensitivity Point-of-Care Whole-Blood Cardiac Troponin I Measurement to Rule Out Acute Myocardial Infarction at Low Risk

Authors:

Apple, Fred S.; Smith, Stephen W.; Greenslade, Jaimi H.; Sandoval, Yader; Parsonage, William; Ranasinghe, Isuru; Gaikwad, Niranjan; Schulz, Karen; Stephensen, Laura; Schmidt, Christian W.; Okeson, Brynn; Cullen, Louise; SAMIE Investigators

Point-of-care high-sensitivity troponin-I analysis in capillary blood for acute coronary syndrome diagnostics

Authors:

Bruinen, Anne L.; Frenk, Lisa D. S.; de Theije, Femke; Kemper, Daniëlle W. M.; Janssen, Marcel J. W.; Rahel, Braim M.; Meeder, Joan G.; van ‘t Hof, Arnoud W. J.

Diagnostic performance of a rapid, novel, whole blood, point of care high-sensitivity cardiac troponin I assay for myocardial infarction

Authors:

Gunsolus, Ian L.; Schulz, Karen; Sandoval, Yader; Smith, Stephen W.; Lindgren, Brittany; Okeson, Brynn; Apple, Fred S.

POCT-management during the first wave of Covid-19 in France. Results of a national survey leaded by the SFBC-POCT Working Group

Authors:

Glady, Ludovic; Moal, Valérie; Benz-De Bretagne, Isabelle; Bouvier, Damien; Di Giovanni, Flore; Chenevier-Gobeaux, Camille; Jeannesson, Elise; Jolly, Emilie; Kadi, Habiba; Oueidat, Nathalie; Pernet, Pascal; Pieroni, Laurence; Poupon, Carole; Toussaint-Hacquard, Marie; Dubos, Mickaël; Martinel, Isabelle; Chauzit, Emmanuelle; Beauvieux, Marie-Christine

Prehospital troponin as a predictor of early clinical deterioration

Authors:

Martín-Rodríguez, Francisco; Sanz-García, Ancor; Castro-Portillo, Enrique; Delgado-Benito, Juan F.; Del Pozo Vegas, Carlos; Ortega Rabbione, Guillermo; Martín-Herrero, Francisco; Martín-Conty, José Luis; López-Izquierdo, Raúl

Determination of sex-specific 99th percentile upper reference limits for a point of care high sensitivity cardiac troponin I assay

Authors:

Apple, Fred S.; Schulz, Karen; Schmidt, Christian W.; van Domburg, Trees S. Y.; Fonville, Judith M.; de Theije, Femke K.

Implementation of High-Sensitivity and Point-of-Care Cardiac Troponin Assays into Practice: Some Different Thoughts

Authors:

Fred S Apple , Corinne R Fantz , Paul O Collinson , the IFCC Committee on Clinical Application of Cardiac Bio-Markers

Accuracy of pre-hospital HEART score risk classification using point of care versus high sensitive troponin in suspected NSTE-ACS

Authors:

van Dongen, Dominique N.; Fokkert, Marion J.; Tolsma, Rudolf T.; van der Sluis, Aize; Slingerland, Robbert J.; Badings, Erik A.; van ‘t Hof, Arnoud W.J.; Ottervanger, Jan Paul

Impact of Point‐of‐care Testing on Length of Stay of Patients in the Emergency Department: A Cluster‐randomized Controlled Study

Authors:

Hausfater, Pierre; Hajage, David; Bulsei, Julie; Canavaggio, Pauline; Lafourcade, Alexandre; Paquet, Anne Laure; Arock, Michel; Durand‐Zaleski, Isabelle; Riou, Bruno; Oueidat, Nathalie

Point-of-care testing: place of France in the worldNational survey in healthcare establisments in 2019

Authors:

Beauvieux, Marie-Christine; Bost, Erika; Castaing-Mouhica, Gladys; Terral, Catherine; Berthon, Nathalie; Martinel, Isabelle; Chauzit, Emmanuelle

Point-of-Care Troponin Testing during Ambulance Transport to Detect Acute Myocardial Infarction

Authors:

Stopyra, Jason P.; Snavely, Anna C.; Scheidler, James F.; Smith, Lane M.; Nelson, Robert D.; Winslow, James E.; Pomper, Gregory J.; Ashburn, Nicklaus P.; Hendley, Nella W.; Riley, Robert F.; Koehler, Lauren E.; Miller, Chadwick D.; Mahler, Simon A.

Development of a needle shaped microelectrode for electrochemical detection of the sepsis biomarker interleukin-6 (IL-6) in real time

Authors:

Russell, Christopher; Ward, Andrew C.; Vezza, Vincent; Hoskisson, Paul; Alcorn, David; Steenson, D. Paul; Corrigan, Damion K.

Evaluation of the capillary assay of C-reactive protein (CRP) through the lenght of consultation in pediatric emergencies and its economic impact

Authors:

Roulliaud, Marine; Pereira, Bruno; Cosme, Justine; Mourgues, Charline; Sarret, Catherine; Sapin, Vincent; Caron, Nicolas; Bouvier, Damien

A prospective, multi-centre US clinical trial to determine accuracy of FebriDx point-of-care testing for acute upper respiratory infections with and without a confirmed fever

Authors:

Shapiro, Nathan I.; Self, Wesley H.; Rosen, Jeffrey; Sharp, Stephan C.; Filbin, Michael R.; Hou, Peter C.; Parekh, Amisha D.; Kurz, Michael C.; Sambursky, Robert

A point-of-care microfluidic biochip for quantification of CD64 expression from whole blood for sepsis stratification

Authors:

Hassan, U.; Ghonge, T.; Reddy, B.; Patel, M.; Rappleye, M.; Taneja, I.; Tanna, A.; Healey, R.; Manusry, N.; Price, Z.; Jensen, T.; Berger, J.; Hasnain, A.; Flaugher, E.; Liu, S.; Davis, B.; Kumar, J.; White, K.; Bashir, R.

Use of point-of-care testing and early assessment model reduces length of stay for ambulatory patients in an emergency department

Authors:

Kankaanpää, Meri; Raitakari, Maria; Muukkonen, Leila; Gustafsson, Siv; Heitto, Merja; Palomäki, Ari; Suojanen, Kimmo; Harjola, Veli-Pekka

Point-of-care troponinT is inferior to high-sensitivity troponinT for ruling out acute myocardial infarction in the emergency department.

Authors:

Ewoud Ter Avest, Anniek Visser, Bram Reitsma, Rob Breedveld, Albert Wolthuis

Addition of copeptin improves diagnostic performance of point-of-care testing (POCT) for cardiac troponin T in early rule-out of myocardial infarction — A pilot study

Authors:

Vafaie, Mehrshad; Biener, Moritz; Mueller, Matthias; Abu Sharar, Haitham; Hartmann, Oliver; Hertel, Sabine; Katus, Hugo A.; Giannitsis, Evangelos

Comparison between B·R·A·H·M·S PCT direct, a new sensitive point-of-care testing device for rapid quantification of procalcitonin in emergency department patients and established reference methods – a prospective multinational trial

Authors:

Kutz, Alexander; Hausfater, Pierre; Oppert, Michael; Alan, Murat; Grolimund, Eva; Gast, Claire; Alonso, Christine; Wissmann, Christoph; Kuehn, Christian; Bernard, Maguy; Huber, Andreas; Mueller, Beat; Schuetz, Philipp

Economic Analysis of Rapid and Sensitive Polymerase Chain Reaction Testing in the Emergency Department for Influenza Infections in Children

Authors:

Nelson, Richard E.; Stockmann, Chris; Hersh, Adam L.; Pavia, Andrew T.; Korgenksi, Kent; Daly, Judy A.; Couturier, Marc R.; Ampofo, Krow; Thorell, Emily A.; Doby, Elizabeth H.; others

Comprehensive bedside point of care testing in critical ED patients: a before and after study

Authors:

Singer, Adam J.; Williams, Justin; Taylor, Maria; Le Blanc, Deborah; Thode, Henry C.

Narrative review of primary care point-of-care testing (POCT) and antibacterial use in respiratory tract infection (RTI)

Authors:

Cooke, Jonathan; Butler, Christopher; Hopstaken, Rogier; Dryden, Matthew Scott; McNulty, Cliodna; Hurding, Simon; Moore, Michael; Livermore, David Martin

Analytical evaluation of point of care cTnT and clinical performances in an unselected population as compared with central laboratory highly sensitive cTnT

Authors:

Dupuy, Anne Marie; Sebbane, Mustapha; Roubille, François; Coste, Thibault; Bargnoux, Anne Sophie; Badiou, Stéphanie; Kuster, Nils; Cristol, Jean Paul

The Effect of Laboratory Testing on Emergency Department Length of Stay: A Multihospital Longitudinal Study Applying a Cross-classified Random-effect Modeling Approach

Authors:

Li, Ling; Georgiou, Andrew; Vecellio, Elia; Eigenstetter, Alex; Toouli, George; Wilson, Roger; Westbrook, Johanna I.

Point-of-care testing in the overcrowded emergency department–can it make a difference?

Authors:

Rooney, Kevin D.; Schilling, Ulf M.

Diagnostic Characteristics of a Clinical Screening Tool in Combination With Measuring Bedside Lactate Level in Emergency Department Patients With Suspected Sepsis

Authors:

Singer, Adam J.; Taylor, Merry; Domingo, Anna; Ghazipura, Saad; Khorasonchi, Adam; Thode, Henry C.; Shapiro, Nathan I.