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1.
PLoS Biol ; 20(2): e3001285, 2022 02.
Article in English | MEDLINE | ID: mdl-35104285

ABSTRACT

Amid the Coronavirus Disease 2019 (COVID-19) pandemic, preprints in the biomedical sciences are being posted and accessed at unprecedented rates, drawing widespread attention from the general public, press, and policymakers for the first time. This phenomenon has sharpened long-standing questions about the reliability of information shared prior to journal peer review. Does the information shared in preprints typically withstand the scrutiny of peer review, or are conclusions likely to change in the version of record? We assessed preprints from bioRxiv and medRxiv that had been posted and subsequently published in a journal through April 30, 2020, representing the initial phase of the pandemic response. We utilised a combination of automatic and manual annotations to quantify how an article changed between the preprinted and published version. We found that the total number of figure panels and tables changed little between preprint and published articles. Moreover, the conclusions of 7.2% of non-COVID-19-related and 17.2% of COVID-19-related abstracts undergo a discrete change by the time of publication, but the majority of these changes do not qualitatively change the conclusions of the paper.


Subject(s)
COVID-19/prevention & control , Information Dissemination/methods , Peer Review, Research/trends , Periodicals as Topic/trends , Publications/trends , COVID-19/epidemiology , COVID-19/virology , Humans , Pandemics/prevention & control , Peer Review, Research/methods , Peer Review, Research/standards , Periodicals as Topic/standards , Periodicals as Topic/statistics & numerical data , Publications/standards , Publications/statistics & numerical data , Publishing/standards , Publishing/statistics & numerical data , Publishing/trends , SARS-CoV-2/isolation & purification , SARS-CoV-2/physiology
2.
PLoS Biol ; 19(4): e3000959, 2021 04.
Article in English | MEDLINE | ID: mdl-33798194

ABSTRACT

The world continues to face a life-threatening viral pandemic. The virus underlying the Coronavirus Disease 2019 (COVID-19), Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), has caused over 98 million confirmed cases and 2.2 million deaths since January 2020. Although the most recent respiratory viral pandemic swept the globe only a decade ago, the way science operates and responds to current events has experienced a cultural shift in the interim. The scientific community has responded rapidly to the COVID-19 pandemic, releasing over 125,000 COVID-19-related scientific articles within 10 months of the first confirmed case, of which more than 30,000 were hosted by preprint servers. We focused our analysis on bioRxiv and medRxiv, 2 growing preprint servers for biomedical research, investigating the attributes of COVID-19 preprints, their access and usage rates, as well as characteristics of their propagation on online platforms. Our data provide evidence for increased scientific and public engagement with preprints related to COVID-19 (COVID-19 preprints are accessed more, cited more, and shared more on various online platforms than non-COVID-19 preprints), as well as changes in the use of preprints by journalists and policymakers. We also find evidence for changes in preprinting and publishing behaviour: COVID-19 preprints are shorter and reviewed faster. Our results highlight the unprecedented role of preprints and preprint servers in the dissemination of COVID-19 science and the impact of the pandemic on the scientific communication landscape.


Subject(s)
COVID-19 , Information Dissemination/methods , Publishing/trends , SARS-CoV-2 , Biomedical Research/trends , COVID-19/epidemiology , Communication , Humans , Open Access Publishing/trends , Pandemics , Peer Review, Research/trends , Preprints as Topic , SARS-CoV-2/pathogenicity
3.
Clin Neuropharmacol ; 41(1): 20-22, 2018.
Article in English | MEDLINE | ID: mdl-29303799

ABSTRACT

OBJECTIVE: To determine the utility of an electronic diary for registering motor fluctuations and dyskinesia in Parkinson disease (PD). METHODS: Free, open-access touch screen software suitable for Android 4.4 or higher, with medication alarms, adjustable intervals, and medication dose settings was developed to evaluate ON-OFF periods and dyskinesia. Prospective evaluation included a first phase conducted to make adjustments concerning motor limitations when using the tablet, as well as for proper motor complication identification, and a second phase of 3 days of use at home with a prior diary training session comparing a modified paper version of Core Assessment Program for Surgical Interventional Therapies in PD and the electronic diary. RESULTS: All patients correctly identified ON-OFF periods and dyskinesia. Rater/patient matching ON-OFF fluctuations ranged between 94% and 100% for evaluations of different motor states. Dyskinesia matching percentage was 100% for patients with dyskinesia interfering with activities of daily living and 88% for those who reported no-interference. No significant differences between paper and electronic diaries were identified when reporting ON-OFF motor states or in the number of errors when filling the diaries. CONCLUSIONS: This electronic motor diary proved to be reliable for ON-OFF state and dyskinesia identification and classification. However, no advantage to paper diary has been observed in terms of number of erroneous entries. Based on these results, to improve home motor fluctuations, detection efforts should be directed toward the development of automatic wearable devices rather than digital versions of current available ON-OFF diaries.


Subject(s)
Dyskinesias/diagnosis , Dyskinesias/etiology , Electronic Health Records , Parkinson Disease/complications , Activities of Daily Living , Aged , Dyskinesias/classification , Female , Humans , Male , Middle Aged , Prospective Studies , Severity of Illness Index
4.
Front Hum Neurosci ; 11: 409, 2017.
Article in English | MEDLINE | ID: mdl-28855866

ABSTRACT

Neural systems are characterized by their complex dynamics, reflected on signals produced by neurons and neuronal ensembles. This complexity exhibits specific features in health, disease and in different states of consciousness, and can be considered a hallmark of certain neurologic and neuropsychiatric conditions. To measure complexity from neurophysiologic signals, a number of different nonlinear tools of analysis are available. However, not all of these tools are easy to implement, or able to handle clinical data, often obtained in less than ideal conditions in comparison to laboratory or simulated data. Recently, the temporal structure function emerged as a powerful tool for the analysis of complex properties of neuronal activity. The temporal structure function is efficient computationally and it can be robustly estimated from short signals. However, the application of this tool to neuronal data is relatively new, making the interpretation of results difficult. In this methods paper we describe a step by step algorithm for the calculation and characterization of the structure function. We apply this algorithm to oscillatory, random and complex toy signals, and test the effect of added noise. We show that: (1) the mean slope of the structure function is zero in the case of random signals; (2) oscillations are reflected on the shape of the structure function, but they don't modify the mean slope if complex correlations are absent; (3) nonlinear systems produce structure functions with nonzero slope up to a critical point, where the function turns into a plateau. Two characteristic numbers can be extracted to quantify the behavior of the structure function in the case of nonlinear systems: (1). the point where the plateau starts (the inflection point, where the slope change occurs), and (2). the height of the plateau. While the inflection point is related to the scale where correlations weaken, the height of the plateau is related to the noise present in the signal. To exemplify our method we calculate structure functions of neuronal recordings from the basal ganglia of parkinsonian and healthy rats, and draw guidelines for their interpretation in light of the results obtained from our toy signals.

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