Impact of serial cardiopulmonary point-of-care ultrasound exams in patients with acute dyspnoea: A randomised, controlled trial

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Impact of serial cardiopulmonary point-of-care ultrasound exams in patients with acute dyspnoea : A randomised, controlled trial. / Arvig, Michael Dan; Lassen, Annmarie Touborg; Gæde, Peter Haulund; Gärtner, Stefan Wernblad; Falster, Casper; Skov, Inge Raadal; Petersen, Henrik Ømark; Posth, Stefan; Laursen, Christian B.

I: Emergency Medicine Journal, Bind 40, Nr. 10, 2023, s. 700-707.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Arvig, MD, Lassen, AT, Gæde, PH, Gärtner, SW, Falster, C, Skov, IR, Petersen, HØ, Posth, S & Laursen, CB 2023, 'Impact of serial cardiopulmonary point-of-care ultrasound exams in patients with acute dyspnoea: A randomised, controlled trial', Emergency Medicine Journal, bind 40, nr. 10, s. 700-707. https://doi.org/10.1136/emermed-2022-212694

APA

Arvig, M. D., Lassen, A. T., Gæde, P. H., Gärtner, S. W., Falster, C., Skov, I. R., Petersen, H. Ø., Posth, S., & Laursen, C. B. (2023). Impact of serial cardiopulmonary point-of-care ultrasound exams in patients with acute dyspnoea: A randomised, controlled trial. Emergency Medicine Journal, 40(10), 700-707. https://doi.org/10.1136/emermed-2022-212694

Vancouver

Arvig MD, Lassen AT, Gæde PH, Gärtner SW, Falster C, Skov IR o.a. Impact of serial cardiopulmonary point-of-care ultrasound exams in patients with acute dyspnoea: A randomised, controlled trial. Emergency Medicine Journal. 2023;40(10):700-707. https://doi.org/10.1136/emermed-2022-212694

Author

Arvig, Michael Dan ; Lassen, Annmarie Touborg ; Gæde, Peter Haulund ; Gärtner, Stefan Wernblad ; Falster, Casper ; Skov, Inge Raadal ; Petersen, Henrik Ømark ; Posth, Stefan ; Laursen, Christian B. / Impact of serial cardiopulmonary point-of-care ultrasound exams in patients with acute dyspnoea : A randomised, controlled trial. I: Emergency Medicine Journal. 2023 ; Bind 40, Nr. 10. s. 700-707.

Bibtex

@article{b2a5f82b1a8e49d28c47dfec9b41e148,
title = "Impact of serial cardiopulmonary point-of-care ultrasound exams in patients with acute dyspnoea: A randomised, controlled trial",
abstract = "Background Serial point-of-care ultrasound (PoCUS) can potentially improve acute patient care through treatment adjusted to the dynamic ultrasound findings. The objective was to investigate if treatment guided by monitoring patients with acute dyspnoea with serial cardiopulmonary PoCUS and usual care could reduce the severity of dyspnoea compared with usual care alone. Methods This was a randomised, controlled, blinded-outcome trial conducted in three EDs in Denmark between 9 October 2019 and 26 May 2021. Patients aged ≥18 years admitted with a primary complaint of dyspnoea were allocated 1:1 with block randomisation to usual care, which included a single cardiopulmonary PoCUS within 1 hour of arrival (control group) or usual care (including a PoCUS within 1 hour of arrival) plus two additional PoCUS performed at 2 hours interval from the initial PoCUS (serial ultrasound group). The primary outcome was a reduction of dyspnoea measured on a verbal dyspnoea scale (VDS) from 0 to 10 recorded at inclusion and after 2, 4 and 5 hours. Results There were 206 patients recruited, 102 in the serial ultrasound group and 104 in the control group, all of whom had complete follow-up. The mean difference in VDS between patients in the serial ultrasound and the control group was -1.09 (95% CI -1.51 to -0.66) and -1.66 (95% CI -2.09 to -1.23) after 4 and 5 hours, respectively. The effect was more pronounced in patients with a presumptive diagnosis of acute heart failure (AHF). A larger proportion of patients received diuretics in the serial ultrasound group. Conclusion Therapy guided by serial cardiopulmonary PoCUS may, together with usual care, facilitate greater improvement in the severity of dyspnoea, especially in patients with AHF compared with usual care with a single PoCUS in the ED. Serial PoCUS should therefore be considered for routine use to aid the physician in stabilising the patient faster. Trial registration number NCT04091334. ",
keywords = "acute care, acute medicine, crowding, respiratory, ultrasonography",
author = "Arvig, {Michael Dan} and Lassen, {Annmarie Touborg} and G{\ae}de, {Peter Haulund} and G{\"a}rtner, {Stefan Wernblad} and Casper Falster and Skov, {Inge Raadal} and Petersen, {Henrik {\O}mark} and Stefan Posth and Laursen, {Christian B.}",
note = "Publisher Copyright: {\textcopyright} Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.",
year = "2023",
doi = "10.1136/emermed-2022-212694",
language = "English",
volume = "40",
pages = "700--707",
journal = "Emergency Medicine Journal",
issn = "1472-0205",
publisher = "B M J Group",
number = "10",

}

RIS

TY - JOUR

T1 - Impact of serial cardiopulmonary point-of-care ultrasound exams in patients with acute dyspnoea

T2 - A randomised, controlled trial

AU - Arvig, Michael Dan

AU - Lassen, Annmarie Touborg

AU - Gæde, Peter Haulund

AU - Gärtner, Stefan Wernblad

AU - Falster, Casper

AU - Skov, Inge Raadal

AU - Petersen, Henrik Ømark

AU - Posth, Stefan

AU - Laursen, Christian B.

N1 - Publisher Copyright: © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

PY - 2023

Y1 - 2023

N2 - Background Serial point-of-care ultrasound (PoCUS) can potentially improve acute patient care through treatment adjusted to the dynamic ultrasound findings. The objective was to investigate if treatment guided by monitoring patients with acute dyspnoea with serial cardiopulmonary PoCUS and usual care could reduce the severity of dyspnoea compared with usual care alone. Methods This was a randomised, controlled, blinded-outcome trial conducted in three EDs in Denmark between 9 October 2019 and 26 May 2021. Patients aged ≥18 years admitted with a primary complaint of dyspnoea were allocated 1:1 with block randomisation to usual care, which included a single cardiopulmonary PoCUS within 1 hour of arrival (control group) or usual care (including a PoCUS within 1 hour of arrival) plus two additional PoCUS performed at 2 hours interval from the initial PoCUS (serial ultrasound group). The primary outcome was a reduction of dyspnoea measured on a verbal dyspnoea scale (VDS) from 0 to 10 recorded at inclusion and after 2, 4 and 5 hours. Results There were 206 patients recruited, 102 in the serial ultrasound group and 104 in the control group, all of whom had complete follow-up. The mean difference in VDS between patients in the serial ultrasound and the control group was -1.09 (95% CI -1.51 to -0.66) and -1.66 (95% CI -2.09 to -1.23) after 4 and 5 hours, respectively. The effect was more pronounced in patients with a presumptive diagnosis of acute heart failure (AHF). A larger proportion of patients received diuretics in the serial ultrasound group. Conclusion Therapy guided by serial cardiopulmonary PoCUS may, together with usual care, facilitate greater improvement in the severity of dyspnoea, especially in patients with AHF compared with usual care with a single PoCUS in the ED. Serial PoCUS should therefore be considered for routine use to aid the physician in stabilising the patient faster. Trial registration number NCT04091334.

AB - Background Serial point-of-care ultrasound (PoCUS) can potentially improve acute patient care through treatment adjusted to the dynamic ultrasound findings. The objective was to investigate if treatment guided by monitoring patients with acute dyspnoea with serial cardiopulmonary PoCUS and usual care could reduce the severity of dyspnoea compared with usual care alone. Methods This was a randomised, controlled, blinded-outcome trial conducted in three EDs in Denmark between 9 October 2019 and 26 May 2021. Patients aged ≥18 years admitted with a primary complaint of dyspnoea were allocated 1:1 with block randomisation to usual care, which included a single cardiopulmonary PoCUS within 1 hour of arrival (control group) or usual care (including a PoCUS within 1 hour of arrival) plus two additional PoCUS performed at 2 hours interval from the initial PoCUS (serial ultrasound group). The primary outcome was a reduction of dyspnoea measured on a verbal dyspnoea scale (VDS) from 0 to 10 recorded at inclusion and after 2, 4 and 5 hours. Results There were 206 patients recruited, 102 in the serial ultrasound group and 104 in the control group, all of whom had complete follow-up. The mean difference in VDS between patients in the serial ultrasound and the control group was -1.09 (95% CI -1.51 to -0.66) and -1.66 (95% CI -2.09 to -1.23) after 4 and 5 hours, respectively. The effect was more pronounced in patients with a presumptive diagnosis of acute heart failure (AHF). A larger proportion of patients received diuretics in the serial ultrasound group. Conclusion Therapy guided by serial cardiopulmonary PoCUS may, together with usual care, facilitate greater improvement in the severity of dyspnoea, especially in patients with AHF compared with usual care with a single PoCUS in the ED. Serial PoCUS should therefore be considered for routine use to aid the physician in stabilising the patient faster. Trial registration number NCT04091334.

KW - acute care

KW - acute medicine

KW - crowding

KW - respiratory

KW - ultrasonography

U2 - 10.1136/emermed-2022-212694

DO - 10.1136/emermed-2022-212694

M3 - Journal article

C2 - 37595984

AN - SCOPUS:85170224454

VL - 40

SP - 700

EP - 707

JO - Emergency Medicine Journal

JF - Emergency Medicine Journal

SN - 1472-0205

IS - 10

ER -

ID: 370567397