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The Effect of Blood Pressure on Cerebral Perfusion During Vascular Surgery

26 september 2017 uppdaterad av: Niels Damkjær Olesen, Rigshospitalet, Denmark

The Effect of Blood Pressure on Cerebral Perfusion and Oxygenation During Vascular Surgery

Anesthesia reduces blood pressure and cerebral blood flow is normally considered to be maintained despite marked changes in blood pressure. Vascular surgical patients are often elderly, have high blood pressure and atherosclerosis and in these patients cerebral blood flow may decrease if blood pressure is reduced during anesthesia. The purpose of this study is to assess the effect of blood pressure for preservation of cerebral blood flow during anesthesia in vascular surgery. The hypothesis is that in vascular surgical patients, during anesthesia, cerebral blood flow is higher with blood pressure maintained at a higher level than that used in normal clinical practice.

Studieöversikt

Detaljerad beskrivning

Background: Induction of anesthesia reduces mean arterial pressure (MAP) and cerebral blood flow is normally considered to be maintained by cerebral autoregulation despite changes in MAP between 60 - 150 mmHg and standard of care during anesthesia is to maintain MAP above 60 mmHg. Vascular surgical patients are often elderly with hypertension and atherosclerotic manifestations that may impair cerebral autoregulation of importance for anesthesia-induced reduction in blood pressure.

Objective: To assess the effect of MAP for preservation of cerebral blood flow and oxygenation during vascular surgery.

Hypothesis: The primary hypothesis is that during general anesthesia in vascular surgical patients, cerebral blood flow velocity and oxygenation is higher with MAP maintained at 80-90 mmHg, compared with a MAP maintained at a minimum of 60 mmHg.

MAP is controlled in both groups using continuous infusion of phenylephrine. Phenylephrine is used as a tool in order to assess the effect of MAP on the cerebral circulation. In both groups, central blood volume is optimized by infusion of lactated Ringer´s solution using a goal directed fluid therapy following induction of anaesthesia and before commencement of phenylephrine infusion.

Trial size: The investigators will include 40 participants (2 x 20) in order to detect or reject a 20% difference in middle cerebral artery velocity with a type I error risk of 5% and a type II error risk of 20% (power at 80%). Interim analysis will be conducted after inclusion of 20 patients (2 x 10). Excluded patients will be replaced.

Studietyp

Interventionell

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

      • Copenhagen Ø, Danmark, 2100
        • Rigshospitalet, Anæstesi og Operationsklinikken 2043

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

19 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Patients undergoing one of the following vascular surgical interventions in general anesthesia: Infra-inguinal bypass, femoro-femoral cross-over bypass or iliofemoral bypass surgery.
  • Age > 18 years. Informed consent

Exclusion Criteria:

  • Use of monoamine oxidase inhibitors
  • Allergy to phenylephrine
  • Patients that cannot cooperate during examination
  • Dementia defined as Mini-Mental State Examination < 24
  • Anesthesia within the last 30 days
  • Alcohol consumption at or above 420 grams per week
  • Lack of fluency in written and spoken Danish
  • Severe hearing and vision impairment
  • Neurological disease

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Stödjande vård
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Trippel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: MAP maintained at 80 mmHg
During anesthesia MAP is maintained at 80 - 90 mmHg MAP using continuous infusion of phenylephrine.
Intervention group, MAP is maintained at 80 - 90 mmHg during anesthesia using continuous infusion of phenylephrine.
Aktiv komparator: MAP maintained at 60 mmHg
During anesthesia MAP is maintained at minimum of 60 mmHg using continuous infusion of phenylephrine.
Control group, MAP is maintained at minimum of 60 mmHg during anesthesia using continuous infusion of phenylephrine.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Middle cerebral artery blood velocity
Tidsram: During surgery
Middle cerebral artery blood velocity measured in [cm/s] assessed by transcranial Doppler. Changes in middle cerebral artery blood velocity reflects changes in cerebral blood flow.
During surgery

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in serum S100B as compared between subjects in the control- and intervention groups
Tidsram: Blood is sampled 10 min prior to induction of anesthesia and at the end of surgery
Serum concentrations of S100B, a marker of neuronal injury
Blood is sampled 10 min prior to induction of anesthesia and at the end of surgery
Change in serum neuron-specific enolase as compared between subjects in the control- and intervention groups
Tidsram: Blood is sampled 10 min prior to induction of anesthesia and at the end of surgery
Serum concentrations of neuron-specific enolase, a marker of neuronal injury
Blood is sampled 10 min prior to induction of anesthesia and at the end of surgery
Regional cerebral oxygenation as compared between subjects in the control- and intervention groups
Tidsram: During surgery
Frontal lobe oxygenation measured as the percentage of oxyhemoglobin of total hemoglobin [%] evaluated by near-infrared spectroscopy
During surgery
Cardiac output as compared between subjects in the control- and intervention groups
Tidsram: During surgery
Cardiac output measured in [l/min] evaluated by pulse contour analysis of the arterial blood pressure curve
During surgery
Stroke volume as compared between subjects in the control- and intervention groups
Tidsram: During surgery
Stroke volume measured in [ml/min] evaluated by pulse contour analysis of the arterial blood pressure curve
During surgery

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Niels D. Olesen, MD, Rigshospitalet, Anæstesi og Operationsklinikken 2043, Denmark

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Förväntat)

1 mars 2017

Primärt slutförande (Förväntat)

1 november 2017

Avslutad studie (Förväntat)

1 november 2017

Studieregistreringsdatum

Först inskickad

14 augusti 2015

Först inskickad som uppfyllde QC-kriterierna

20 augusti 2015

Första postat (Uppskatta)

24 augusti 2015

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

28 september 2017

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

26 september 2017

Senast verifierad

1 september 2017

Mer information

Termer relaterade till denna studie

Läkemedels- och apparatinformation, studiedokument

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produkt tillverkad i och exporterad från U.S.A.

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