Intra-aortic balloon pump does not influence cerebral hemodynamics and neurological outcomes in high-risk cardiac patients undergoing cardiac surgery: an analysis of the IABCS trial

Juliana R Caldas, Ronney B Panerai, Edson Bor-Seng-Shu, Graziela S R Ferreira, Ligia Camara, Rogério H Passos, Angela M Salinet, Daniel S Azevedo, Marcelo de-Lima-Oliveira, Filomena R B G Galas, Julia T Fukushima, Ricardo Nogueira, Fabio S Taccone, Giovanni Landoni, Juliano P Almeida, Thompson G Robinson, Ludhmila A Hajjar, Juliana R Caldas, Ronney B Panerai, Edson Bor-Seng-Shu, Graziela S R Ferreira, Ligia Camara, Rogério H Passos, Angela M Salinet, Daniel S Azevedo, Marcelo de-Lima-Oliveira, Filomena R B G Galas, Julia T Fukushima, Ricardo Nogueira, Fabio S Taccone, Giovanni Landoni, Juliano P Almeida, Thompson G Robinson, Ludhmila A Hajjar

Abstract

Background: The intra-aortic balloon pump (IABP) is often used in high-risk patients undergoing cardiac surgery to improve coronary perfusion and decrease afterload. The effects of the IABP on cerebral hemodynamics are unknown. We therefore assessed the effect of the IABP on cerebral hemodynamics and on neurological complications in patients undergoing cardiac surgery who were randomized to receive or not receive preoperative IABP in the 'Intra-aortic Balloon Counterpulsation in Patients Undergoing Cardiac Surgery' (IABCS) trial.

Methods: This is a prospectively planned analysis of the previously published IABCS trial. Patients undergoing elective coronary artery bypass surgery with ventricular ejection fraction ≤ 40% or EuroSCORE ≥ 6 received preoperative IABP (n = 90) or no IABP (n = 91). Cerebral blood flow velocity (CBFV) of the middle cerebral artery through transcranial Doppler and blood pressure through Finometer or intra-arterial line were recorded preoperatively (T1) and 24 h (T2) and 7 days after surgery (T3) in patients with preoperative IABP (n = 34) and without IABP (n = 33). Cerebral autoregulation was assessed by the autoregulation index that was estimated from the CBFV response to a step change in blood pressure derived by transfer function analysis. Delirium, stroke and cognitive decline 6 months after surgery were recorded.

Results: There were no differences between the IABP and control patients in the autoregulation index (T1: 5.5 ± 1.9 vs. 5.7 ± 1.7; T2: 4.0 ± 1.9 vs. 4.1 ± 1.6; T3: 5.7 ± 2.0 vs. 5.7 ± 1.6, p = 0.97) or CBFV (T1: 57.3 ± 19.4 vs. 59.3 ± 11.8; T2: 74.0 ± 21.6 vs. 74.7 ± 17.5; T3: 71.1 ± 21.3 vs. 68.1 ± 15.1 cm/s; p = 0.952) at all time points. Groups were not different regarding postoperative rates of delirium (26.5% vs. 24.2%, p = 0.83), stroke (3.0% vs. 2.9%, p = 1.00) or cognitive decline through analysis of the Mini-Mental State Examination (16.7% vs. 40.7%; p = 0.07) and Montreal Cognitive Assessment (79.16% vs. 81.5%; p = 1.00).

Conclusions: The preoperative use of the IABP in high-risk patients undergoing cardiac surgery did not affect cerebral hemodynamics and was not associated with a higher incidence of neurological complications. Trial registration http://www.clinicaltrials.gov (NCT02143544).

Keywords: Cardiopulmonary bypass; Cerebral autoregulation; IABP; Transcranial Doppler.

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Study flow chart. IABP intra-aortic balloon pump, AI aortic insufficiency, AMI acute myocardial infarction
Fig. 2
Fig. 2
Ten-second continuous recording of blood pressure and cerebral blood flow velocity from 63-year-old male patient with IABP ratio 1:3, showing removal of the intra-aortic balloon pump at t = 6 s. This subject is representative of the frequent occurrence of cerebral blood flow velocity diastolic values that are negative or near zero following deflation of the balloon (Reproduced with permission from Caldas et al. [22])
Fig. 3
Fig. 3
Mean values (± 1 standard error) of ARI for control group population (white bar) and intra-aortic balloon pump population (black bar), followed by the session number corresponding to before the surgery (T1), 24 h (T2) and 7 days (T3) of follow-up
Fig. 4
Fig. 4
Control group (dotted line) and intra-aortic balloon pump group (continuous line) population averages of cerebral blood flow velocity step response. Before surgery (a) and 24 h (b) and 7 days after surgery (c). Largest ± 1 standard error is represented at the point of occurrence

References

    1. Newman MF, Grocott HP, Mathew JP, White WD, Landolfo K, Reves JG, et al. Report of the substudy assessing the impact of neurocognitive function on quality of life 5 years after cardiac surgery. Stroke. 2001;32:2874–2881. doi: 10.1161/hs1201.099803.
    1. Scolletta S, Taccone FS, Donadello K. Brain injury after cardiac surgery. Minerva Anestesiol. 2015;81:662–677.
    1. Salazar JD, Wityk RJ, Grega MA, Borowicz LM, Doty JR, Petrofski JA, et al. Stroke after cardiac surgery: short- and long-term outcomes. Ann Thorac Surg. 2001;72:2. doi: 10.1016/S0003-4975(01)02929-0.
    1. Cropsey C, Kennedy J, Han J, Pandharipande P. Cognitive dysfunction, delirium, and stroke in cardiac surgery patients. Semin Cardiothorac Vasc Anesth. 2015;19:309–317. doi: 10.1177/1089253215570062.
    1. Baskett RJ, Ghali WA, Maitland A, Hirsch GM. The intraaortic balloon pump in cardiac surgery. Ann Thorac Surg. 2002;74:1276–1287. doi: 10.1016/S0003-4975(02)03663-9.
    1. Dunkman WB, Leinbach RC, Buckley MJ, Mundth ED, Kantrowitz AR, Austen WG, et al. Clinical and hemodynamic results of intraaortic balloon pumping and surgery for cardiogenic shock. Circulation. 1972;46:465–477. doi: 10.1161/01.CIR.46.3.465.
    1. Cheung AT, Levy WJ, Weiss SJ, Barclay DK, Stecker MM. Relationships between cerebral blood flow velocities and arterial pressures during intra-aortic counterpulsation. J Cardiothorac Vasc Anesth. 1998;12:51–57. doi: 10.1016/S1053-0770(98)90055-6.
    1. Schachtrupp A, Wrigge H, Busch T, Buhre W, Weyland A. Influence of intra-aortic balloon pumping on cerebral blood flow pattern in patients after cardiac surgery. Eur J Anaesthesiol. 2005;22:165–170. doi: 10.1097/00003643-200503000-00001.
    1. Pfluecke C, Christoph M, Kolschmann S, Tarnowski D, Forkmann M, Jellinghaus S, et al. Intra-aortic balloon pump (IABP) counterpulsation improves cerebral perfusion in patients with decreased left ventricular function. Perfusion. 2014;29:511–516. doi: 10.1177/0267659114525218.
    1. Brass LM. Reversed intracranial blood flow in patients with an intra-aortic balloon pump. Stroke. 1990;21:484–487. doi: 10.1161/01.STR.21.3.484.
    1. Appelboom G, Strozyk D, Hwang BY, Prowda J, Badjatia N, Helbok R, et al. Bedside use of a dual aortic balloon occlusion for the treatment of cerebral vasospasm. Neurocrit Care. 2010;13:385–388. doi: 10.1007/s12028-010-9442-2.
    1. Ducruet AF, Albuquerque FC, Crowley RW, Williamson R, Forseth J, McDougall CG. Balloon-pump counterpulsation for management of severe cardiac dysfunction after aneurysmal subarachnoid hemorrhage. World Neurosurg. 2013;80:347. doi: 10.1016/j.wneu.2012.05.029.
    1. Glick RE, Sanders KM, Stern TA. Failure to record delirium as a complication of intra-aortic balloon pump treatment: a retrospective study. J Geriatr Psychiatry Neurol. 1996;9:97–99. doi: 10.1177/089198879600900205.
    1. Trabold B, Metterlein T. Postoperative delirium: risk factors, prevention, and treatment. J Cardiothorac Vasc Anesth. 2014;28:1352–1360. doi: 10.1053/j.jvca.2014.03.017.
    1. Honet JC, Wajszczuk WJ, Rubenfire M, Kantrowitz A, Raikes JA. Neurological abnormalities in the leg(s) after use of intraaortic balloon pump: report of six cases. Arch Phys Med Rehabil. 1975;56:346–352.
    1. Beholz S, Braun J, Ansorge K, Wollert HG, Eckel L. Paraplegia caused by aortic dissection after intraaortic balloon pump assist. Ann Thorac Surg. 1998;65:603–604. doi: 10.1016/S0003-4975(97)01274-5.
    1. Kunt A, Atbas C, Hidiroglu M, Cetin L, Erdogan KE, Kucuker A, et al. Predictors and outcomes of minor cerebrovascular events after cardiac surgery: a multivariable analysis of 1346 patients. J Cardiovasc Surg. 2013;54:537–543.
    1. Cruz-Flores S, Diamond AL, Leira EC. Cerebral air embolism secondary to intra-aortic balloon pump rupture. Neurocrit Care. 2005;2:49–50. doi: 10.1385/NCC:2:1:049.
    1. Ferreira GSR, de Almeida JP, Landoni G, Vincent JL, Fominskiy E, Galas FRBG, et al. Effect of a perioperative intra-aortic balloon pump in high-risk cardiac surgery patients: a randomized clinical trial. Crit Care Med. 2018;46:e742–e750. doi: 10.1097/CCM.0000000000003185.
    1. Gosling RG, Budge MM. Terminology for describing the elastic behavior of arteries. Hypertens Dallas Tex. 1979;2003(41):1180–1182.
    1. Panerai RB, White RP, Markus HS, Evans DH. Grading of cerebral dynamic autoregulation from spontaneous fluctuations in arterial blood pressure. Stroke J Cereb Circ. 1998;29:2341–2346. doi: 10.1161/01.STR.29.11.2341.
    1. Caldas JR, Panerai RB, Bor-Seng-Shu E, Almeida JP, Ferreira GSR, Camara L, et al. Cerebral hemodynamics with intra-aortic balloon pump: business as usual? Physiol Meas. 2017;38:1349–1361. doi: 10.1088/1361-6579/aa68c4.
    1. Tiecks FP, Lam AM, Aaslid R, Newell DW. Comparison of static and dynamic cerebral autoregulation measurements. Stroke. 1995;26:1014–1019. doi: 10.1161/01.STR.26.6.1014.
    1. Panerai RB, Haunton VJ, Hanby MF, Salinet AS, Robinson TG. Statistical criteria for estimation of the cerebral autoregulation index (ARI) at rest. Physiol Meas. 2016;37:661–672. doi: 10.1088/0967-3334/37/5/661.
    1. Patel N, Panerai RB, Haunton V, Katsogridakis E, Saeed NP, Salinet A, et al. The Leicester cerebral haemodynamics database: normative values and the influence of age and sex. Physiol Meas. 2016;37:1485–1498. doi: 10.1088/0967-3334/37/9/1485.
    1. Inouye SK, van Dyck CH, Alessi CA, Balkin S, Siegal AP, Horwitz RI. Clarifying confusion: the confusion assessment method. A new method for detection of delirium. Ann Intern Med. 1990;113:941–948. doi: 10.7326/0003-4819-113-12-941.
    1. Ely E, Inouye SK, Bernard GR, et al. Delirium in mechanically ventilated patients: validity and reliability of the confusion assessment method for the intensive care unit (cam-icu) JAMA. 2001;286:2703–2710. doi: 10.1001/jama.286.21.2703.
    1. Folstein MF, Folstein SE, McHugh PR. “Mini-mental state”. A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975;12:189–198. doi: 10.1016/0022-3956(75)90026-6.
    1. Nasreddine ZS, Phillips NA, Bedirian V, Charbonneau S, Whitehead V, Collin I, et al. The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc. 2005;53:695–699. doi: 10.1111/j.1532-5415.2005.53221.x.
    1. Moulopoulos SD, Topaz S, Kolff WJ. Diastolic balloon pumping (with carbon dioxide) in the aorta—a mechanical assistance to the failing circulation. Am Heart J. 1962;63:669–675. doi: 10.1016/0002-8703(62)90012-1.
    1. Weber KT, Janicki JS. Intraaortic balloon counterpulsation. A review of physiological principles, clinical results, and device safety. Ann Thorac Surg. 1974;17:602–636. doi: 10.1016/S0003-4975(10)65706-2.
    1. Yang F, Jia Z, Xing J, Wang Z, Liu Y, Hao X, et al. Effects of intra-aortic balloon pump on cerebral blood flow during peripheral venoarterial extracorporeal membrane oxygenation support. J Transl Med. 2014;12:106. doi: 10.1186/1479-5876-12-106.
    1. Petroni T, Harrois A, Amour J, Lebreton G, Brechot N, Tanaka S, et al. Intra-aortic balloon pump effects on macrocirculation and microcirculation in cardiogenic shock patients supported by venoarterial extracorporeal membrane oxygenation. Crit Care Med. 2014;42:2075–2082. doi: 10.1097/CCM.0000000000000410.
    1. Bellapart J, Geng S, Dunster K, Timms D, Barnett AG, Boots R, et al. Intraaortic balloon pump counterpulsation and cerebral autoregulation: an observational study. BMC Anesthesiol. 2010;10:3. doi: 10.1186/1471-2253-10-3.
    1. Claassen JA, Meel-van den Abeelen AS, Simpson DM, Panerai RB. Transfer function analysis of dynamic cerebral autoregulation: a white paper from the International Cerebral Autoregulation Research Network. J Cereb Blood Flow Metab Off J Int Soc Cereb Blood Flow Metab. 2016;36:665–680. doi: 10.1177/0271678X15626425.
    1. Ringelstein EB. Transcranial Doppler Monitoring. In: Aaslid R, editor. Transcranial Doppler Sonogr. Vienna: Springer Vienna; 1986. pp. 147–163.
    1. Voulgaris SG, Partheni M, Kaliora H, Haftouras N, Pessach IS, Polyzoidis KS. Early cerebral monitoring using the transcranial Doppler pulsatility index in patients with severe brain trauma. Med Sci Monit. 2005;11:CR49–CR52.
    1. de Riva N, Budohoski KP, Smielewski P, Kasprowicz M, Zweifel C, Steiner LA, et al. Transcranial Doppler pulsatility index: what it is and what it isn’t. Neurocrit Care. 2012;17:58–66. doi: 10.1007/s12028-012-9672-6.
    1. Zweifel C, Czosnyka M, Carrera E, de Riva N, Pickard JD, Smielewski P. Reliability of the blood flow velocity pulsatility index for assessment of intracranial and cerebral perfusion pressures in head-injured patients. Neurosurgery. 2012;71:853–861. doi: 10.1227/NEU.0b013e3182675b42.
    1. Morgalla MH, Magunia H. Noninvasive measurement of intracranial pressure via the pulsatility index on transcranial Doppler sonography: is improvement possible? J Clin Ultrasound JCU. 2016;44:40–45. doi: 10.1002/jcu.22279.
    1. Ono M, Zheng Y, Joshi B, Sigl JC, Hogue CW. Validation of a stand-alone near-infrared spectroscopy system for monitoring cerebral autoregulation during cardiac surgery. Anesth Analg. 2013;116:198–204. doi: 10.1213/ANE.0b013e318271fb10.
    1. Ono M, Arnaoutakis GJ, Fine DM, Brady K, Easley RB, Zheng Y, et al. Blood pressure excursions below the cerebral autoregulation threshold during cardiac surgery are associated with acute kidney injury. Crit Care Med. 2013;41:464–471. doi: 10.1097/CCM.0b013e31826ab3a1.
    1. Caldas JR, Haunton VJ, Panerai RB, Hajjar LA, Robinson TG. Cerebral autoregulation in cardiopulmonary bypass surgery: a systematic review. Interact Cardiovasc Thorac Surg. 2017;26:494–503. doi: 10.1093/icvts/ivx357.
    1. Cavallazzi R, Saad M, Marik PE. Delirium in the ICU: an overview. Ann Intensive Care. 2012;2:49. doi: 10.1186/2110-5820-2-49.
    1. Saczynski JS, Marcantonio ER, Quach L, Fong TG, Gross A, Inouye SK, et al. Cognitive trajectories after postoperative delirium. N Engl J Med. 2012;367:30–39. doi: 10.1056/NEJMoa1112923.
    1. Koster S, Hensens AG, Schuurmans MJ, van der Palen J. Risk factors of delirium after cardiac surgery: a systematic review. Eur J Cardiovasc Nurs. 2011;10:197–204. doi: 10.1016/j.ejcnurse.2010.09.001.
    1. Inouye SK, Foreman MD, Mion LC, Katz KH, Cooney LM., Jr Nurses’ recognition of delirium and its symptoms: comparison of nurse and researcher ratings. Arch Intern Med. 2001;161:2467–2473. doi: 10.1001/archinte.161.20.2467.
    1. Patel N, Banahan C, Janus J, Horsfield MA, Cox A, Li X, et al. Perioperative cerebral microbleeds after adult cardiac surgery. Stroke. 2019;50:336–343. doi: 10.1161/STROKEAHA.118.023355.
    1. Murkin JM, Newman SP, Stump DA, Blumenthal JA. Statement of consensus on assessment of neurobehavioral outcomes after cardiac surgery. Ann Thorac Surg. 1995;59:1289–1295. doi: 10.1016/0003-4975(95)00106-U.
    1. Selnes OA, Gottesman RF, Grega MA, Baumgartner WA, Zeger SL, McKhann GM. Cognitive and neurologic outcomes after coronary-artery bypass surgery. N Engl J Med. 2012;366:250–257. doi: 10.1056/NEJMra1100109.
    1. Selnes OA, Grega MA, Borowicz LM, Jr, Royall RM, McKhann GM, Baumgartner WA. Cognitive changes with coronary artery disease: a prospective study of coronary artery bypass graft patients and nonsurgical controls. Ann Thorac Surg. 2003;75:6. doi: 10.1016/S0003-4975(03)00021-3.
    1. Mullges W, Berg D, Schmidtke A, Weinacker B, Toyka KV. Early natural course of transient encephalopathy after coronary artery bypass grafting. Crit Care Med. 2000;28:1808–1811. doi: 10.1097/00003246-200006000-00020.
    1. Serrador JM, Picot PA, Rutt BK, Shoemaker JK, Bondar RL. MRI measures of middle cerebral artery diameter in conscious humans during simulated orthostasis. Stroke. 2000;31:1672–1678. doi: 10.1161/01.STR.31.7.1672.
    1. Sammons EL, Samani NJ, Smith SM, Rathbone WE, Bentley S, Potter JF, et al. Influence of noninvasive peripheral arterial blood pressure measurements on assessment of dynamic cerebral autoregulation. J Appl Physiol. 2007;103:369–375. doi: 10.1152/japplphysiol.00271.2007.

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