Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Gasping Improves Long-term Survival After Out-of-hospital Cardiac Arrest

19. december 2016 opdateret af: Jiri Malek, Charles University, Czech Republic

Agonal Breathing is a Positive Predictive Factor of Long Term Survival After Out-of-hospital Cardiac Arrest

The aim of our retrospective clinical study was to examine the association between agonal breathing, return of spontaneous circulation (ROSC), and long-term survival. A secondary aim was to examine role of basic life support (BLS) and response time. Our hypothesis is that agonal breathing has positive effects on both primary and secondary endpoints.

Studieoversigt

Status

Afsluttet

Detaljeret beskrivelse

Aims Agonal breathing ("gasping for air") has previously been found to be associated with the outcomes of out-of-hospital cardiac arrest (OHCA) patients on which resuscitation was attempted. On the other hand, little is known, about agonal breathing with regard to whether it is a positive factor for survival after hospital admission and how it relates to the patient's future quality of life. For this reason we have undertaken a retrospective study using a comprehensive emergency medical service (EMS) database from the Central Bohemian region of the Czech Republic. The primary endpoint of the study was to assess if agonal breathing present when EMS arrives has a positive impact on the six-month survival of OHCA patients, which was independent of other factors like EMS response time and BLS provision. The secondary endpoints sought to determine if agonal breathing positively impacts ROSC and an evaluation of various factors that can influence agonal breathing, specifically response time and provision of BLS.

Method The data were recorded using the Utstein protocol. Only anonymized data were used for analysis. The data were derived from the EMS registry of the Central Bohemian Region, which is the largest EMS in the Czech Republic. The study sample included all OHCA cases, of presumed cardiac origin, that where resuscitated by the EMS between 1st July 2013 and 30th June 2014 (n = 584). Two subsequent patient outcomes: (1) return of spontaneous circulation (defined as spontaneous circulation at hospital admission) and (2) six-month survival were assessed in patients with and without agonal breathing. Six-month survival data of OHCA patients of presumed cardiac origin was derived from administrative insurance registries or medical records of patients, with only aggregated data being available.

Factors that may influence the presence of agonal breathing, specifically BLS provision before a professional EMS team reached the patient and second, EMS team response times, were also examined. BLS provision by lay persons was reported by the first-on-scene EMS team as (yes/no) and phone assisted CPR was registered by the dispatcher as (yes/no). BLS was considered to have been provided if any of the following activities (1) resuscitation by a bystander, (2) phone assisted CPR, or (3) both were recorded as having been performed. The response time was calculated as the elapsed time between recorded activation of an EMS team and the on scene arrival time.

Other covariates such as age and sex were also available and analyzed. The initial difference in response time between the groups was assessed using the T-test. For categorical variables, the chi-square test was used. Simple and multivariate logistic regression models were used to assess relationships between factors related to the presence of agonal breathing and ROSC. A p-value of < 0.05 was considered statistically significant.

Undersøgelsestype

Observationel

Tilmelding (Faktiske)

584

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Barn
  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Sandsynlighedsprøve

Studiebefolkning

Victims of primary out-of-hospital cardiac arrest

Beskrivelse

Inclusion Criteria: all out-of-hospital cardiac arrest cases, of presumed cardiac origin, that where resuscitated by the emergency medical service of Central Bohemia region between 1st July 2013 and 30th June 2014 (n = 584) -

Exclusion Criteria: other than non-cardiac cause of cardiac arrest

-

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Observationsmodeller: Case-Control
  • Tidsperspektiver: Fremadrettet

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
association between agonal breathing and long-term survival
Tidsramme: 6 months after successful resuscitation
6 months after successful resuscitation

Sekundære resultatmål

Resultatmål
Tidsramme
impact of agonal breathing on return of spontaneous circulation
Tidsramme: immediately after resuscitation
immediately after resuscitation

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. juli 2013

Primær færdiggørelse (Faktiske)

1. juni 2014

Studieafslutning (Faktiske)

1. november 2016

Datoer for studieregistrering

Først indsendt

16. december 2016

Først indsendt, der opfyldte QC-kriterier

19. december 2016

Først opslået (Skøn)

20. december 2016

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

20. december 2016

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

19. december 2016

Sidst verificeret

1. december 2016

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • Gasping1

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Abonner