Category Definition · Beyond Brain Health™

Perioperative Brain
Optimization

The emerging clinical practice of measuring and strengthening brain resilience before, during, and after surgery — and the evidence base that makes it clinically urgent.

AuthorSandra Bargeron, PA-C, CAA
Dataset2,062 NSRI™ completers
References127 peer-reviewed
AudiencePatients & Clinicians
Definition

What Is Perioperative Brain Optimization?

In the world of perioperative care, we rarely pause to ask the most basic question about the brain: are we doing enough to protect and strengthen it before surgery?

Most research on post-operative cognitive decline has centered on cognitive assessments — tools like the MoCA or MMSE that capture a snapshot of current function. But they only tell us where a patient stands at a single point in time. They don't show us brain resilience, or what could be changed to help the brain recover from the stress of surgery.

Perioperative brain optimization means taking stock of this landscape — measuring the brain's reserve, its vulnerabilities, and its modifiable factors — and working to shore it up before the stress arrives.

After 16 years and more than 10,000 anesthesia cases, I saw firsthand the missed opportunities to measure and support the brain's ability to recover from surgery. Research shows five main neurologic domains that we can measure and strengthen: cardiometabolic health, medication and pain management, sleep and circadian rhythms, lifestyle choices, and brain and social health. This work led to the creation of the NSRI™.

Why It Matters

The Scale of the Problem

Surgery is not a niche medical event. It is a universal human experience — and the brain is always in the room.

0%
of Americans undergo surgery annually
Bicket MC et al. PubMed Central, 2024
0%
of older surgical patients develop POCD within one week
Vlisides P et al. Maturitas, 2025
0%
of high-risk elderly patients experience postoperative delirium
Inouye SK et al. Lancet, 2014
higher dementia risk after a single episode of surgical delirium
Gordon EH et al. BMJ, 2024
0
average surgical or invasive procedures in a lifetime
Lee P et al. J Am Coll Surg, 2008
0%
of dementia cases attributable to modifiable risk factors
Lancet Commission on Dementia, 2024

Standard preoperative protocols focus on cardiac and pulmonary function, medication reconciliation, and surgical risk — while neglecting neurologic resilience assessment entirely.

This is not a minor gap. It is a system-wide blind spot.

Research Window Data

What 2,062 Assessments Revealed

The NSRI™ research window (closed March 19, 2026) generated the first large-scale dataset of preoperative neurologic resilience — from a health-literate, self-advocating population.

Research Window
0
total completers
Mean NSRI score: 65.9 · SD 13.8 · Range: 8–99
Elevated / High Risk
0%
scored NSRI < 60
In a health-engaged, proactively-screened population
Bottleneck Prevalence
0%
carry ≥1 Bottleneck factor
Most unidentified by standard preoperative intake
TBI History
0%
prior head injury
Vast majority unaccounted for in standard screening
Prior Delirium
0%
prior surgical delirium history
Chronically underdiagnosed in standard care
Construct Validity
r = 0.91
base reserve → final score
Internal consistency supporting NSRI™ architecture
Source: NSRI™ V2.5 Research Window Dataset — 2,062 completers, research window closed March 19, 2026. Sandra Bargeron, PA-C, CAA · Beyond Brain Health™
Evidence Foundation

Five Converging Research Streams

Perioperative brain optimization is not a hypothesis — it is the clinical convergence of five independently established bodies of literature.

01

Dementia Prevention Science — The Lancet Commissions

Landmark reports in 2017, 2020, and 2024 showing ~45% of dementia cases are attributable to 14 modifiable risk factors. The perioperative period is when these factors become immediately relevant — a surgery date is the deadline.

Livingston G et al. Lancet. 2024Lancet. 2020Lancet. 2017
02

Perioperative Neuroscience — POCD & Delirium Literature

The 2018 Nomenclature Consensus established the clinical taxonomy for perioperative neurocognitive disorders. The ASA Brain Health Initiative (2019) and APSF (2024) identified delirium prevention as a patient safety priority. An umbrella review identified 73 independent risk factors for POCD.

Evered L et al. Br J Anaesth. 2018 [Landmark]APSF Advisory Group. 2024
03

Cardiometabolic Risk — D1 Domain

Metabolic syndrome raises postoperative delirium risk ~1.85×. Insulin resistance independently predicts POCD (AUC 0.742). Blood pressure, lipid dysregulation, and weight are each independently linked to perioperative cognitive risk.

Feinkohl I et al. Br J Anaesth. 2023 [Landmark]Chen Y et al. Front Aging Neurosci. 2019
04

Medication & Pain Burden — D2 Domain

Anticholinergic burden: OR 1.5–3.0 for cognitive adverse effects. Benzodiazepine use: OR 2.0–4.6 for dementia. Chronic widespread pain: 2.55× increased MCI risk (UK Biobank, n=188,594). Benzodiazepine-induced deficits can persist months to years after discontinuation.

Gray SL et al. JAMA Intern Med. 2015 [Landmark]Billioti de Gage S et al. BMJ. 2014 [Landmark]
05

Sleep & Circadian Health — D3 Domain (Highest Impact)

Sleep is the single most impactful modifiable domain in the NSRI™ dataset — strongest domain predictor (r=0.681), highest coefficient of variation (CV=31.6%). Preoperative sleep disturbance: OR 2.8 for POCD. In the research window, 17.8% scored below 10/20 on sleep.

D3 Sleep r=0.681 · CV=31.6% · 17.8% scored <10/20 · Strongest modifiable intervention target
Shi L et al. Sleep Med Rev. 2018Flink BJ et al. Anesthesiology. 2012
The NSRI™ Framework

Five Domains of Neurologic Resilience

Each domain is independently evidence-based, independently modifiable, and independently measured in the NSRI™.

D1 · Cardiometabolic Health

Cardiovascular and metabolic reserve — blood pressure control, glucose regulation, lipid management, metabolic syndrome, and insulin resistance — all directly shape how the brain handles surgical stress.

Uncontrolled metabolic factors are among the most modifiable brain risks in the preoperative window. They are also where measurable changes can be made fastest.

For clinicians: Metabolic syndrome raises postoperative delirium risk ~1.85×. Insulin resistance predicts POCD with AUC 0.742.
For patients: Blood pressure, blood sugar, and weight are the three most actionable variables before surgery.
76.8%
Population mean score (16.9/22)
r=0.628
Correlation with final NSRI score
1.85×
Delirium risk with metabolic syndrome
Historical Vulnerability

The Bottleneck Index™

Beyond modifiable domain scores, the NSRI™ captures a second distinct construct: historical vulnerability.

The Bottleneck Index™ is a multiplicative modifier derived from 10 history sections covering prior neurologic events, traumatic brain injury, surgical history, cancer treatment, connective tissue and autonomic disorders, hormonal transitions, neuroinflammatory infections, and functional frailty.

In the research window dataset, 96.2% of completers carry at least one Bottleneck factor. The Bottleneck Index correlates with the final score at r=−0.710.

Each additional Bottleneck factor suppresses the mean NSRI score by 4.6–7.3 points. Moving from 0 to 7 factors drops the mean from 82.2 to 42.1 — a 40-point differential.
Bottleneck FactorsMean NSRI Score
0 factors (3.8%)
82.2
1 factor (14.1%)
76.9
2 factors (23.8%)
71.5
3 factors (21.5%)
66.9
4 factors (17.4%)
60.9
5 factors (10.6%)
54.4
6 factors (6.5%)
49.4
7 factors (2.3%)
42.1
NSRI™ V2.5 Dataset · 2,062 completers · March 2026
The Measurement Standard

The NSRI™ Quantifies.
It Does Not Diagnose.

The Neurologic Stress & Recovery Index™, developed by Sandra Bargeron, PA-C, CAA, is the first assessment tool designed to quantify perioperative brain resilience across five modifiable domains plus historical vulnerability factors. Approximately 81% of scored items are modifiable in the preoperative window.

30.1%
of a health-engaged, proactively-screened population scored elevated or high-risk. None of these vulnerabilities would be identified by standard preoperative intake.

Perioperative brain optimization is not a future discipline. It is a measurable, actionable practice that begins before the next surgical procedure.

Reference Library

Full Reference List

127 verified peer-reviewed references. Key studies listed by domain.

Landmark Studies 6
  1. [1] Livingston G et al. Lancet. 2024;404(10452):572-628.
  2. [2] Livingston G et al. Lancet. 2020;396(10248):413-446.
  3. [3] Livingston G et al. Lancet. 2017;390(10113):2673-2734.
  4. [4] Evered L et al. Br J Anaesth. 2018;121(5):1005-1012.
  5. [54] Gray SL et al. JAMA Intern Med. 2015;175(3):401-407.
  6. [58] Billioti de Gage S et al. BMJ. 2014;349:g5205.
Perioperative Neuroscience & POCD 7
  1. [5] Mahanna-Gabrielli E et al. Br J Anaesth. 2019;123(4):464-478.
  2. [6] Vlisides P, Bhattacharya S. Maturitas. 2025;194:108148.
  3. [7] Taffett NT et al. J Clin Med. 2023;12(4):1610.
  4. [10] Inouye SK et al. Lancet. 2014;383(9920):911-922.
  5. [21] APSF Brain Health Patient Safety Priority Advisory Group. 2024.
  6. [138] Ahmadzadeh S et al. Cureus. 2025;17(9):e92927.
  7. [139] Gordon EH et al. BMJ. 2024;384:e077634.
Cardiometabolic Domain (D1) 3
  1. [45] Biessels GJ et al. Lancet Neurol. 2006;5(1):64-74.
  2. [87] Chen Y et al. Front Aging Neurosci. 2019;11:197.
  3. [88] Feinkohl I et al. Br J Anaesth. 2023;131(2):338-347.
Medication & Pain Domain (D2) 4
  1. [54] Gray SL et al. JAMA Intern Med. 2015;175(3):401-407.
  2. [58] Billioti de Gage S et al. BMJ. 2014;349:g5205.
  3. [61] Jiang X et al. Anesthesiology. 2025;143(6):1560-1571.
  4. [107] Crowe SF, Stranks EK. Arch Clin Neuropsychol. 2018;33(7):901-911.
Sleep & Circadian Domain (D3) 3
  1. [63] Shi L et al. Sleep Med Rev. 2018;40:4-16.
  2. [65] Flink BJ et al. Anesthesiology. 2012;116(4):788-796.
  3. [66] Gupta R et al. Sleep Med Clin. 2022;17(3):467-482.
Bottleneck Index™ & Historical Vulnerability 3
  1. [22] Gu D et al. Neuroepidemiology. 2022;56(1):4-16.
  2. [128] Khan A et al. Biology (Basel). 2025;14(6):640.
  3. [133] Terrando N et al. Ann Neurol. 2011;70(6):986-995.
Full reference library at beyondbrainhealth.com/nsri-evidence