These reporter systems have been invaluable to researchers’ understanding of transcriptional fidelity because they allowed genes, alleles, and molecular mechanisms to be identified that directly regulate the fidelity of transcription. However, they only report on errors in artificially damaged templates, or within highly specific genetic contexts, which limits the scientific questions they can answer. An important advantage of the C-seq protocol is that it monitors the fidelity of transcription throughout the entire transcriptome5, greatly expanding the scientific knowledge of the accuracy with which genetic information is expressed. Secondly, because the C-seq assay utilizes RNA as its source material, it is likely that this assay can be adapted to any organism of choice, obviating the need to generate complicated reporter constructs for each transgenic model. This protocol also has advantages over existing massively parallel sequencing approaches17,22.
This is in contrast to the 9 wrong patient errors (0.58%) identified through the HCS transcription error queue. Only 4 other types of errors (wrong drug, wrong dose, omission, and overt error not otherwise classified) were formally reported. Over 3 months of data collection, 1,563 NMTEs identified by pharmacists were reported in the HCS transcription error queue, corresponding to an overall error detection rate of 0.34%.
During that time, only 12 NMTEs identified by pharmacists were reported through what is one way to check for an error caused by transposed numbers? the institution’s formal reporting system, corresponded to an overall error detection rate of 0.0026%. Previously, the institution actively tracked medication errors via an internally developed formal, comprehensive, anonymous, Web-based, error-reporting form. Institution policy encouraged the reporting of all medication errors, including near misses. Upon completion of an error report by an individual, data from the error report are entered into a Microsoft Access database and are given a series of “tags” and other identifiers that allow different types of errors to be grouped together and trended. In the 3 months preceding data collection for the current study, a total of 294 events were reported through this pathway. Of these 294 events, 68 stemmed from the transcription node and 24 of which could be classified as near misses.
Notably, transcription errors, although transient in nature, may result in heritable changes in cellular phenotypes, as has been indicated in studies utilizing the lac operon in bacteria (Gordon et al., 2009, 2013; Gamba and Zenkin, 2017). Additionally, it should be stressed that RNAs are not just templates for protein synthesis, but can interact with proteins, DNA and other RNAs, and can have catalyzing properties themselves. The notion that RNAs could switch to other functional states by the introduction of error-induced sequence differences should be explored further. To stop transcription errors from taking place a good process for quality control is important. Just implementing some spell-checking software could reduce greatly transcription errors taking place.
Another study defined MTEs as incomplete and/or wrong transcription of a medication order 7. Garcia-Ramos and Baldominos Utrilla described MTEs as when the medication prescription did not match with what was transcribed on the nurse’s administration form 18. In Fahimi et al., MTEs were defined as deviations in transcription of medication orders from the previous step, this could occur on an order sheet, notes, and/or documentations in the pharmacy database 11. Finally, Lisby et al. defined MTEs as discrepancies in the names of the drugs, their formulations, routes of administration, doses, dosing regimens, omission of drugs, or addition of drugs which were not ordered or prescribed 19. A transcription error is a mistake made when a person is performing data entry from one form of recorded documentation to another, usually a computer-oriented text document or electronic records system.
For example, RNA polymerases have long been known to be error-prone in vitro1,2, and recently it was shown that they commit errors in vivo as well3,5,6, particularly when confronted with DNA damage7,8,9,10. Taken together, these observations indicate that transcription errors occur continuously in all living cells, suggesting that they could be a potent source of mutated proteins. Misspelling a medication’s name was considered a MTE when the misspelling was major and might lead difficulty recognizing the medication. Similarly, the panelists were divisive to recording transactions decide whether to consider omission of the transcriber’s signature as a MTE error or not when the guidelines require so.
For example, while several labs have devised valuable reporter assays for the study of transcriptional mutagenesis, these assays are only able to measure transcription errors in a limited number of contexts and model organisms4,15. To overcome these limitations, many researchers have turned to RNA sequencing technology (RNA-seq), which theoretically allows transcription errors to be recorded throughout the transcriptome of any species. However, these studies are easily confounded by library construction artifacts, such as reverse transcription errors, PCR amplification errors, and the error-prone nature of sequencing itself.
Consensus was achieve to accept the definition and to consider 69 of the 76 proposed scenarios (77.6%) as MTEs, exclude 3 scenarios (3.9%), and 4 scenarios (5.3%) remained equivocal. https://www.bookstime.com/ Equivocal scenarios might be considered as MTEs or not depending on the clinical situation. The articles and research support materials available on this site are educational and are not intended to be investment or tax advice. All such information is provided solely for convenience purposes only and all users thereof should be guided accordingly.
To the best of our knowledge, this is the first study in which MTEs are addressed using a formal consensus technique. Medication errors are defined differently and many definition of medication errors were previously reported 13,14,15. Obviously, methodological variation in defining what constitutes a medication error might have a significant impact on the error rates researchers disseminate in their studies reporting on medication errors 8, 9, 16, 17. Researchers might use different definitions or scenarios representing medication error situations which ultimately would lead to variability in error rates reported in their studies. Therefore, defining medication errors is a step of paramount importance in analyzing the incidence and prevalence of medication errors in a particular setting. Formal consensus techniques have been used to reduce discrepancies in what constitutes a medication error and to achieve consensus on definitions and scenarios representing error situations.