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the frequency of intravenous medication administration errors related to smart infusion pumps: a multihospital observational study - what is a smart board

the frequency of intravenous medication administration errors related to smart infusion pumps: a multihospital observational study  -  what is a smart board

Despite the use of smart pumps, intravenous medication errors still exist.
This indicates the need for a standardized method of measuring errors and highlights the importance of identifying issues related to the administration of smart pump medication in order to improve patient safety.
Objective we conducted a multi-site study to investigate the type and frequency of intravenous medication errors associated with smart pumps in the United States.
Methods 10 hospitals of different sizes from different suppliers were involved using smart pumps.
Data were collected using a forward-looking point prevalence approach to capture errors related to drugs taken through smart pumps and to assess their potential hazards.
Results a total of 478 patients and 1164 medication were evaluated.
In the observed infusion, 699 (60%)
One or more errors related to their management.
Errors found, such as labeling errors and bypassing smart pumps and drug depots, are primarily related to violations of hospital policies.
These types of errors can lead to medication errors.
According to the National Coordination Committee on Drug error reporting and prevention (NCC MERP).
Class 1 E error (0. 1%)
Class D 4 (0. 3%)
Class C 492 (
Excluding deviations from hospital policies)(42%)
Confirmed.
Among them, the most common mistakes are unauthorized drug treatment, bypass smart pumps, and error rates.
Conclusion despite the use of smart pumps, we found a high error rate for intravenous medication.
However, there are relatively few potentially harmful errors.
The results of this study will help to develop interventions to eliminate errors during intravenous medication.
Despite the use of smart pumps, intravenous medication errors still exist.
This indicates the need for a standardized method of measuring errors and highlights the importance of identifying issues related to the administration of smart pump medication in order to improve patient safety.
Objective we conducted a multi-site study to investigate the type and frequency of intravenous medication errors associated with smart pumps in the United States.
Methods 10 hospitals of different sizes from different suppliers were involved using smart pumps.
Data were collected using a forward-looking point prevalence approach to capture errors related to drugs taken through smart pumps and to assess their potential hazards.
Results a total of 478 patients and 1164 medication were evaluated.
In the observed infusion, 699 (60%)
One or more errors related to their management.
Errors found, such as labeling errors and bypassing smart pumps and drug depots, are primarily related to violations of hospital policies.
These types of errors can lead to medication errors.
According to the National Coordination Committee on Drug error reporting and prevention (NCC MERP).
Class 1 E error (0. 1%)
Class D 4 (0. 3%)
Class C 492 (
Excluding deviations from hospital policies)(42%)
Confirmed.
Among them, the most common mistakes are unauthorized drug treatment, bypass smart pumps, and error rates.
Conclusion despite the use of smart pumps, we found a high error rate for intravenous medication.
However, there are relatively few potentially harmful errors.
The results of this study will help to develop interventions to eliminate errors during intravenous medication.
Foot bottom contributors KOC, MS, CSY, SL and DWB: contributed to the concept and design of data and results, analysis and interpretation, drafting and writing of articles, for important knowledge content and final approval of the version to be released, it is subject to critical changes.
JA, DA, RC, CC, DLC, AD, LF, CAG-
P, MMH, RRM, NM, JM, SR, ER, DS, MDS, lp, KDS and EW: contributed analysis and interpretation of data and results to oversee data collection at each site, as well as drafting and writing of articles, for important knowledge content and final approval of the version to be released, make critical changes to it.
TWV: critical conception and revision of the paper for important intellectual content.
Fund the Carefusion Foundation;
Medical Device Promotion Association (AAMI).
No one declared a competitive interest.
Ethical approval partner of medical institution Review Committee.
Uncommissioned source and peer review;
External peer review.

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After the splicing screen is added with the touch frame, the large screen interaction can be realized, which can be better introduced and publicized by adding the touch frame, and the splicing screen can have the effect of realizing multi-person interactive touch wall, therefore, after the touch frame is added, the use of the splicing screen is more abundant, the configuration requirements for the splicing screen system are lower, and the flexible space for installing the touch frame is larger,
The teaching all-in-one machine must be familiar to everyone, from the earlier computer projector to the present interaction and teaching.
In this era of continuous influx of information technology, the intelligent touch all-in-one machine is well known as the fifth media besides paper media, radio, television and the Internet.
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