Neurological Patients for Nonneurosurgeries


Neurological diseases affect the functions of the central nervous system (CNS) and the neuromuscular system. Preexisting CNS diseases have important implications regarding the selection of anesthetic drugs, techniques, monitoring, cerebral protection, and resuscitation of the patients. Neurological patients are more sensitive to the anesthetic drugs, and are at risk of perioperative cardiac and respiratory complications. This chapter will include the present recommendations for anesthetic management in patients with various neurological diseases ( Box 47.1 ).

Box 47.1
Neurological Diseases

  • 1.

    Neurodegenerative diseases

    • a.

      Alzheimer disease

    • b.

      Parkinson disease

    • c.

      Huntington disease

    • d.

      Amyotrophic lateral sclerosis

  • 2.

    Demyelinating disease

    • a.

      Guillain-Barré syndrome

    • b.

      Multiple sclerosis

  • 3.

    Neuromuscular disease: myasthenia gravis

  • 4.

    Epilepsy

  • 5.

    Intracranial tumor

  • 6.

    Traumatic brain injury

Neurodegenerative Diseases

Alzheimer Disease

Alzheimer disease (AD) is characterized by an insidious onset and gradually progressive neurodegenerative disease, leading to decline in the intellectual functions. It affects about 4.5 million Americans and remains a major public health problem. It begins initially with forgetfulness and progresses to loss of judgment, complex visual perception defects, language problems, and inability to generate abstract concepts. The major anesthesiologist’s concern during the perioperative period is dealing with a patient who is unable to comprehend and cooperate with those providing medical care.

Anesthetic Considerations ( Table 47.1 )

A few issues must be addressed in the patients with AD. Patients with severe cognitive dysfunction are incapable of giving proper history and consent, so caregivers should be involved in preoperative assessment and preparation. In advanced stage, patients with AD might be disoriented and uncooperative, and make regional anesthesia more difficult. Anesthesia becomes even more challenging in these patients due to interactions of the drugs used for its treatment with the anesthetic agents and the adverse effects of anesthetic agents on the disease progression.

Table 47.1
Anesthetic Considerations of AD
Derangements Management
Special concerns Cognitive dysfunctions Unable to cooperate and give consent or history Caregivers should be involved
High risk for postoperative confusion Predispose to postoperative delirium Sedative premedications should be carefully prescribed
Avoid the drugs and conditions causing delirium
Increased sensitivity to anesthetic agents Smaller doses for sedative–hypnotic drugs are needed
Drug interactions Cholinesterase inhibitors

  • Tacrine

  • Donepezil

  • Rivastigmine

Side effects: nausea, vomiting, diarrhea, and hepatotoxicity
Vagotonic effects of SA and AV node: bradycardia and syncope
Bronchoconstriction
Cholinergic crisis
Prolonged response to succinylcholine
Resistance to nondepolarizing NMBs
MAOIs Profound pressor effect after administration of both indirectly and directly acting sympathomimetic drugs
Antidepressant and psychotomimetic drugs Excessive sedation with concomitant use of anxiolytic and sedative drugs
Regional anesthesia Lesser dose is required to achieve the same sensory level as in patients without AD
AD , Alzheimer disease; AV , atrioventricular; MAOIs , monoamine oxidase Inhibitors; NMBs , neuromuscular blockers; SA , sinoatrial.

Effect of Disease on Anesthesia

These patients are at high risk for postoperative confusion and delirium due to preexisting cognitive impairment. Sedative premedications should be carefully prescribed as these patients are more sensitive to sedative drugs and further increment in mental confusion can occur. Increased sensitivity is attributed to age-related changes in body composition and physiology, causing altered pharmacokinetics and pharmacodynamics of the drugs. There is smaller initial volume of distribution, relative increase in body fat, lower serum albumin, and age-related decline in renal function, which necessitate smaller doses for sedative–hypnotic agents. Other factors that can precipitate delirium; including cerebral hypoxia or hypoperfusion, endocrine or ionic imbalances, postoperative pain, sepsis, and bowel or bladder distention, should be avoided. Use of certain medications such as high-dose steroids, neuroleptics, benzodiazepines, ketamine, tertiary anticholinergics, opioids, histamine H 2 blockers, and droperidol can also precipitate delirium.

Various medications used for the treatment of AD interact with the anesthetic agents. Cholinesterase inhibitors have been reported to prolong the action of succinylcholine and remifentanil, and may cause resistance to nondepolarizing neuromuscular blockers (NMBs). The patients taking monoamine oxidase inhibitors can develop profound pressor effect after administration of both indirectly and directly acting sympathomimetic drugs. If the patient is receiving antidepressants and psychotomimetic drugs preoperatively, there can be exaggerated effect of anxiolytic and sedative agents. So, the patient’s drug chart must be reviewed to avoid severe drug interactions due to polypharmacy.

The requirements for both volatile and intravenous anesthetic agents decline progressively with age. Elderly patients have altered responses to regional anesthesia. The dose of local anesthetic for subarachnoid block, to achieve the same level of sensory blockade, is lesser than the healthy indiviuals. The sensitivity of CNS to the depressant effects of general anesthetic agents is aggravated by severe cortical atrophy and synaptic loss. Hence, lower dosages of sedative and hypnotic agents are required, and the emergence from general anesthesia may be slow.

Effect of Anesthetic Agents on Disease Progression

In the same manner, anesthetic agents also affect the course of this disease. The experimental and animal studies showed that the general anesthetic agents and some perioperative events enhance the molecular mechanisms associated with AD. The use volatile anesthetic agents and hyperventilation increase the amyloid beta levels, and hypothermia leads to profound phosphorylation of tau (τ) protein. The clinical significance of such experimental studies is unclear. The data from retrospective studies fail provide any convincing evidence for an association between anesthetic exposure and the subsequent risk for development of AD. There is no single “best” anesthetic agent or technique for the patients with AD.

To summarize, the goals of anesthetic management of patients with AD are to avoid drug interactions, postoperative delirium, and the drugs and physiological conditions that can aggravate the disease and careful selection of anesthesia technique to maintain hemodynamic stability.

Parkinson Disease

After AD, Parkinson disease (PD) is considered the second most common neurodegenerative disease afflicting about 1 million Americans. In India the crude prevalence of PD ranges from 7 to 328 per 100,000. PD is characterized by unopposed actions of acetylcholine due to decreased levels of dopamine. This disease affects the multiple systems of body and remains a challenge for anesthesiologists.

Anesthetic Considerations

Perioperative challenges of the patient with PD include maintenance of perioperative drug therapy that leads to potential adverse drug interactions, and various other systemic derangements associated with the disease ( Table 47.2 ). Our goal is to prevent the aggravation of symptoms and to maintain the hemodynamics. Perioperative stress can also worsen the disease.

Table 47.2
Anesthetic Considerations of Parkinson’s Disease
Systemic Derangements Management
Special concerns Upper airway dysfunction
Involuntary movements of glottis and supraglottic structures leads to:

  • Intermittent upper airway obstruction

  • Laryngospasm

  • Retained secretions

  • Aspiration

Continue or increase the antiparkinsonian drugs perioperatively
Succinylcholine might be required to relieve the laryngospasm
Respiratory system

  • Aspiration pneumonia

  • Restrictive lung disease secondary to chest wall rigidity

  • Obstructive ventilatory pattern

  • Sawtooth appearance of flow volume loops

Antiaspiration prophylaxis and rapid sequence induction
Postoperative need of mechanical ventilation
Autonomic nervous system

  • Difficulty with salivation and micturition

  • Gastroparesis

  • Defective control of cardiovascular system

  • Postural hypotension and syncope

  • Thermoregulatory dysfunction

  • Seborrhea

Unable to respond to hypovolemia and vasodilation
Potential for perioperative hemodynamic instability
Altered responses to vasopressors such as noradrenaline
Gastrointestinal system

  • Dysphagia and dysmotility leads to pulmonary aspiration

Antacids and Prokinetic drugs should be used
Metoclopramide must be avoided
Domperidone and cisapride are safe
Cardiovascular system

  • Cardiac arrhythmias

  • Dependent edema

  • Orthostatic hypotension

    • Drug induced or disease induced

Vasodilators should be used with caution
Central nervous system

  • Anxiety

  • Confusion

  • Frank psychosis

  • Postoperative delirium

Benzodiazepines for anxiety and antipsychotics for psychosis can have severe side effects, such as oversedation and acute exacerbation of motor symptoms
Drug interactions Malignant syndrome Avoid the withdrawal of antiparkinsonian drugs
On-off phenomenon with levodopa Can be controlled with carbidopa
Regional anesthesia Advantage : side effects of anesthetic agents can be avoided
Disadvantage : patient’s cooperation is a limiting factor

Effect of the Disease on Anesthetic Agents

The short half-life of levodopa (about 90 min) makes its even brief interruption undesirable. Drug interactions might lead to malignant syndrome, characterized by hyperthermia, akinesia, altered consciousness, muscle rigidity, and autonomic dysfunction. Hence, the drug interruption should be brief, and if patients are not able to take oral drugs then intravenous levodopa with carbidopa should be used. Bioavailability of levodopa decreases significantly in patients with gastroparesis as it undergoes first-pass metabolism after absorption from stomach.

Effect of Anesthetic Agents on the Disease

Various agents being used perioperatively can affect the disease course of PD. Volatile anesthetic agents affect dopaminergic circuitry in the brain, but their effect on PD is not known. These agents have been successfully used during deep brain stimulation with intraoperative electrophysiological monitoring. Propofol has both excitatory and inhibitory effects and produces both dyskinesias and ablation of resting tremor, and has also been used successfully during deep brain stimulation surgery. Dexmedetomidine does not interfere with motor symptoms and appears to be safe. Ketamine has a potential of interactions with levodopa due to its sympathomimetic effects. Drugs acting on dopamine receptors (butyrophenones and phenothiazines) can exacerbate PD and should be avoided. In patients with deep brain stimulation coil implanted, the neurostimulator should be switched off during magnetic resonance imaging. In these patients if cautery is required intraoperatively then bipolar mode should be used, and the leads and generator should not be placed in the path from surgical site to the ground plate.

Regional anesthesia is advantageous over general anesthesia, as the side effects of general anesthetic agents can be avoided. Besides this, oral levodopa can be continued preoperatively, during surgery and in early postoperative period, if required. During regional anesthesia the pharyngeal and laryngeal reflexes are intact or at least same as baseline, so chances of aspiration are lesser. The major disadvantage of regional anesthesia is the difficulty in positioning the patient.

To summarize, the patients with PD are associated with multisystem derangements that leads to increased risk of perioperative morbidity and mortality. Our anesthetic goal should be to avoid any drug that can decrease the level of dopamine, and the drugs that interact with anesthetic agents.

Huntington Disease

Huntington disease (HD) is a rare hereditary neurodegenerative disorder. Even if it is genetically transmitted, it usually manifests between 30 and 40 years of age. In 10% of patients there can be juvenile onset of the disease (symptoms beginning before 20 years of age) and death usually occurs 10–30 years after the disease manifestations. HD is characterized by a triad of progressive cognitive deterioration, dementia, and involuntary choreiform movements. This disease affects 5 to 7 persons per 100,000 population.

Anesthetic Considerations ( Table 47.3 )

The literature on anesthetic management for a patient with HD is derived mostly through the case reports and by theoretical complications as per patient’s symptoms.

Table 47.3
Anesthetic Considerations of Huntington Disease
Systemic Involvement Management
Special concerns Central nervous system

  • Dementia

  • Cognitive decline

  • Depression and other psychiatric diseases

Increased sensitivity to anesthetic agents especially benzodiazepines (midazolam)
Motor system

  • Dysphagia

  • Choreiform movements

Pulmonary aspiration risk: antiaspiration prophylaxis and RSI are used
Drug interactions Hypnotic drugs Prolonged apnea after thiopentone
Succinylcholine Abnormal levels of plasma psuedo-cholinesterase
Prolonged paralysis
No evidence of hyperkalemia
Polypharmacy Beware of side effects
Caution about drug interactions
Neurolept malignant syndrome seen with droperidol and metoclopramide in patients receiving tetrabenazine
Regional anesthesia Technically difficult but not contraindicated

Effect of the Disease on Anesthetic Agents

Patients with HD are at risk of pulmonary aspiration due to dysphagia, so antiaspiration prophylaxis and precautions should be taken. These patients can develop prolonged respiratory depression and delayed awakening after general anesthesia, necessitating the use of lower dosage of sedatives and hypnotic agents. This increased sensitivity might be related to altered pharmacokinetics due to nutritional depletion or increased CNS sensitivity due to neurodegeneration. In a few case reports patients with HD experienced a normal anesthetic and postanesthetic course. Use of thiopentone has been reported to cause prolonged apnea in these patients. Tertiary ammonium compounds, such as atropine, should be avoided as these can aggravate the movement disorders. The response to muscle relaxants in patients with HD also varies. These patients might have a high incidence of abnormal plasma cholinesterase that leads to prolonged the muscle relaxation following the use of succinylcholine, but it has been used uneventfully in a few patients. There are no case reports of succinylcholine-induced hyperkalemia. Similarly, both abnormal and normal responses have been reported with nondepolarizing NMBs. A few authors have reported generalized tonic muscle spasms related to shivering during emergence from anesthesia and suggested to maintain normothermia and avoid inhalational agents to prevent shivering. Regional anesthesia is technically difficult because of the continuous uncontrollable movements, but there is no contraindication.

Amyotrophic Lateral Sclerosis

Amyotrophic lateral sclerosis (ALS) is a progressive and debilitating degenerative disease of the CNS that affects 1–2.5 persons per 100,000 population and presents between 50 and 70 years of age. It is marked by loss of both upper and lower motor neurons in the anterior horn of the spinal cord and brainstem nuclei of cranial nerves.

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