Incidence of Postoperative Delirium in Elderly Patients Undergoing Non-cardiac Surgery

The Incidence, Risk Factors and Outcome of Postoperative Delirium in Elderly Patients Undergoing Non-cardiac Surgery: a Prospective Observational Study

Postoperative delirium (POD) is the most common adverse neurologic complication that can occur in patients of any age. Its incidence varies across age groups and is substantially influenced by patient-related risk factors. POD occurs in 17%-61% of major surgical procedures. Several risk factors which contribute to the development of POD include age more than 60 years, pre-existing cognitive dysfunction, presence of comorbidities, sensorial deficits, malnutrition, polypharmacy, impaired physical mobility and frailty. Postoperative delirium has several wide ranging and adverse outcomes that are consistently associated with delirium such as mortality, increased length of hospital stay, and increased hospital costs. A recently devised tool for rapid assessment of delirium is the 4 A's test. It has now been validated for identifying delirium in the surgical population. The proposed prospective observational study will be conducted on 150 patients belonging to ASA Physical Status I-III of either sex, scheduled to undergo non-cardiac surgery under general anaesthesia (GA), requiring at least 24 hours of postoperative inpatient care. This prospective, observational study aims to evaluate the incidence, risk factors and outcomes of postoperative delirium in elderly patients more than 65 years of age undergoing non-cardiac surgery.

Study Overview

• Status: Recruiting
• Conditions: Postoperative Delirium
• Intervention / Treatment: Drug: Sevoflurane; Drug: Desflurane

Detailed Description

The incidence of postoperative delirium (POD) following major surgery ranges from 17% to 61%.POD is the most frequent neurological complication that can occur in both the young and old, and its rate is considerably impacted by patient-related risk issues. The elderly population is believed to be more susceptible to POD, by virtue of being host to conditions such as a variety of comorbidities, malnutrition, concurrent cognitive dysfunction, frailty, sensorial and functional deficits, and polypharmacy.

Risk factors for delirium may be further identified as predisposing factors and precipitating factors. Predisposing factors are those that are present on admission and are not changeable, e.g. age, number and severity of co-morbid medical conditions, sensory impairment, history of cognitive impairment, sleep deprivation, immobility, and dehydration.Precipitating factors are those that trigger delirium while the patient is hospitalized. These may be infections, constipation, bladder catheterisation, procedures involving instrumentation, immobility, and sensory impairment

Postoperative delirium, especially in the elderly, significantly compromises patient recovery and imposes a heavy toll on patient well-being and the healthcare system. Postoperative delirium has several wide-ranging and adverse outcomes associated with it, such as mortality, increased length of hospital stay and increased hospital costs.

Several tools have been developed to track changes in mental status that could point to the onset of delirium. Among the tools employed for this purpose are the Sedation Scale, the Nursing-Delirium Screening Scale (Nu-DESC), and the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU).

However, there is a lack of consensus on the use of an appropriate tool to evaluate delirium in the postoperative period. The 4A's test is a screening instrument that has been designed for rapid and initial assessment of delirium. It has the added advantage of evaluating not only delirium but also postoperative cognitive dysfunction (POCD) which is the second most common complication in elderly surgical patients.

Delirium is a condition that is presumed to be avoidable in 30%-40% of cases which emphasizes the importance of attention to primary prevention.5 After the onset of delirium, little can be done to influence its duration, severity, or the possibility of recurrence. Thus, the necessity for identifying those at risk of developing postoperative delirium. It is imperative that hospitals should implement multimodal non-pharmacologic delirium prevention methods to identify and monitor patients at risk of developing this morbid condition.

There has been scant research in the developing world, including India in the sphere of postoperative delirium, a condition germane to practically all medical specialities and especially in the elderly population. Our study will research POD we expect to obtain evidence that will find the clinical application.

Our study will be focused on evaluating the incidence of POD in the elderly who will be posted for non-cardiac surgical procedures. We will also assess the association of postoperative delirium with risk factors such as frailty, cognitive dysfunction, impaired functional status, presence of comorbidities and polypharmacy. Other postoperative adverse events such as sedation, pain, postoperative nausea and vomiting will be recorded. Patient's length of stay in the hospital (LOS), any unanticipated ICU admission and mortality within 30 days will also be noted.

The following parameters will be recorded in all the patients,

1. Postoperative delirium: It will be evaluated using 4 A's test, three times in the first 24 hours postoperatively. A score of 0 suggests absence of delirium or severe cognitive impairment, score 1-3 suggests presence of possible cognitive impairment, and a score > 4 suggests the presence of delirium/ cognitive impairment.
2. Frailty: All eligible patients will be assessed preoperatively using the 9-point CFS. Score varies from 1-9 with fitness level very fit to terminally ill as depicted in the table
3. Cognitive dysfunction: Preoperative cognition will be assessed using the 5-point Mini-cog test. A score < 4 will be taken as cut-off for impaired cognitive function
4. Impaired physical mobility: All preoperative mobile patients will be subjected to Timed Up and Go (TUG) test. A score of <10 s is normal and score of <20 s need assistance.
5. Intraoperative hemodynamics (pulse, systolic blood pressure, diastolic blood pressure, and mean arterial blood pressure) will be recorded every 5-minutes intraoperatively and every 15-minutes postoperatively in the postoperative care unit (PACU) till discharge. A mean arterial blood pressure <65 mmHg persisting for greater than 5-minutes despite treatment will be defined as an episode of intraoperative hypotension.
6. Postoperative sedation:Sedation will be assessed postoperatively using the Richmond Agitation and Sedation Scale. Score varies from +4 to -5 and patient will be categorised from combative to unarousable as depicted in table.
7. Postoperative pain will be assessed using the 10-point Numeric Rating Scale (NRS)
8. Postoperative nausea and vomiting (PONV) It will be assessed using 3-point Likert scale (0- no nausea and vomiting, 1- nausea only, 2- vomiting)
9. Length of stay in the hospital and any unanticipated ICU admission will be noted.
10. All patients will be followed up postoperatively for 30-days and any occurrence of mortality will be noted.

• Study Type: Observational
• Enrollment (Estimated): 270

Contacts and Locations

• Study Contact: Name: Nitin Sethi, MBBS, DNB; Phone Number: 00911142252523; Email: nitinsethi77@yahoo.co.in
• Study Contact Backup: Name: Bimla Sharma, MBBS, DGO, MD, FICA, MHA; Phone Number: 00911142252523; Email: bimsharma1@gmail.com

Study Locations

• India
  • New Delhi, India, 110060
    • Not yet recruiting
    • Sir Ganga Ram Hospital
    • Contact: P Muralikrishna, MBBS; Phone Number: 00911142252523; Email: muralikrishna960@gmail.com
    • Contact: Bimla Sharma, MBBS, DGO, MD, FICA. MHA; Phone Number: 00911142252523; Email: bimsharma1@gmail.com
    • Principal Investigator: Bimla Sharma, MBBS, DGO, MD, FICA. MHA
    • Principal Investigator: P Muralikrishna Dr, MBBS
    • Principal Investigator: Chand Sahai, MBBS, DA, MD, FICA
    • Principal Investigator: Nitin Sethi, MBBS, DNB
  • Delhi
    • New Delhi, Delhi, India, 110060
      • Recruiting
      • Sir Ganga Ram Hospital
      • Contact: Nitin Sethi, DNB; Phone Number: 009142252523; Email: nitinsethi77@yahoo.co.in

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 65 years and older (Older Adult)
• Accepts Healthy Volunteers: No

• Sampling Method: Probability Sample

Study Population

Patients greater then 65 years age undergoing elective non-cardiac surgical procedures under general anesthesia

Description

Inclusion Criteria:

• Patients of age >65yrs
• Either sex
• ASA physical status I - III
• Elective non-cardiac surgical procedures under general anesthesia
• Clinical Frailty Score (CFS): 1-8
• Patients requiring at least 24 hours of postoperative inpatient care.

Exclusion Criteria:

• Clinical Frailty Score (CFS) of 9
• Patients diagnosed with dementia, severe psychiatric or neurological diseases
• Recent surgery within past 3-months
• History of recent head injury in the preceding 3 months
• Patients with uncompensated cardiovascular disease, hepato-renal insufficiency and uncontrolled endocrine disease
• Patients on anti-depressant, anti-anxiety, anti-convulsant and anti-parkinsonism medications
• Preoperative haemoglobin < 8 gm % and serum albumin < 3.5mg/dl
• Patient inability to give informed consent
• Presence of preoperative delirium as assessed by 4A'S Test (score ≥ 4)

Study Plan

How is the study designed?

Design Details

• Observational Models: Cohort
• Time Perspectives: Prospective

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
Elderly; Patients > 65 years age undergoing non-cardiac surgery will be administered general anesthesia maintained with sevoflurane or desflurane titrated to maintain anaesthesia depth of 50 (BIS score) using bispectral (BIS) index monitioring	Drug: Sevoflurane; Sevoflurane delivery will will be titrated to maintain anaesthesia depth of 50 (BIS score) using bispectral (BIS) index monitioring; Drug: Desflurane; Desflurane delivery will be titrated to maintain anaesthesia depth of 50 (BIS score) using bispectral (BIS) index monitioring

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Incidence of postoperative delirium	Postoperative delirium will be assessed using 4 A's test.A score of 0 suggests absence of delirium or severe cognitive impairment, score 1-3 suggests presence of possible cognitive impairment, and a score > 4 suggests the presence of delirium/ cognitive impairment	From end of surgery till 24 hours postoperatively

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Postoperative Sedation	Postoperative sedation will be assessed using the 10 point Richmond Agitation and Sedation Scale. +4 suggests overtly combative & violent, 0 suggests awake & quiet, and -5 suggets no response to voice or physical stimulation	From end of surgery till 24 hours postoperatively
Postoperative Pain	It will be assessed using the 10-point Numeric Rating Scale (NRS). A score of 0 suggests 'no pain'and score of 10 suggests 'maximum pain'experienced	From end of surgery till 24 hours postoperatively
Postoperative nausea and vomiting	It will be assessed using 3-point likert scale. A score of 0 suggests 'no nausea & vomiting'and a scoe of 2 suggests 'nausea & vomiting present'	From end of surgery till 24 hours postoperatively
Length of hospital stay	The number of days the patient stays in the hospital post surgery till discharge will be recorded.	From end of surgery till discharge from the hospital
Unanticipated intensive care unit (ICU) admission	Any postoperative event necessitating ICU admission will be recorded	From end of surgery till 30 days postoperatively
Mortality	Any mortality occurring within 30 days of surgery will be recorded	From end of surgery till 30 days postoperatively

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Correlation of risk factors with postoperative delirium	Correlation between age more than 75 years, frailty, cognitive dysfunction, impaired physical mobility, comorbidity and polypharmacy with postoperative delirium will be assessed using multivariate or univariate analysis as applicable	From end of surgery till 24 hours postoperatively

Collaborators and Investigators

• Sponsor: Sir Ganga Ram Hospital
• Investigators: Principal Investigator: Nitin Sethi, MBBS, DNB, Sir Ganga Ram Hospital; Study Chair: Bimla Sharma, MBBS, DGO, MD, FICA, MHA, Sir Ganga Ram Hospital; Principal Investigator: Chand Sahai, MBBS, DA, MD, Sir Ganga Ram Hospital; Study Director: Jayashree Sood, MBBS, MD, FFRCA, PGDHHM, FICA, Sir Ganga Ram Hospital

Study record dates

Study Major Dates

• Study Start (Actual): January 14, 2021
• Primary Completion (Estimated): August 1, 2024
• Study Completion (Estimated): September 1, 2024

Study Registration Dates

• First Submitted: January 12, 2021
• First Submitted That Met QC Criteria: January 12, 2021
• First Posted (Actual): January 13, 2021

Study Record Updates

• Last Update Posted (Actual): December 12, 2023
• Last Update Submitted That Met QC Criteria: December 9, 2023
• Last Verified: December 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Mental Disorders; Pathologic Processes; Nervous System Diseases; Postoperative Complications; Neurologic Manifestations; Confusion; Neurobehavioral Manifestations; Neurocognitive Disorders; Delirium; Emergence Delirium; Physiological Effects of Drugs; Central Nervous System Depressants; Anesthetics, General; Anesthetics; Platelet Aggregation Inhibitors; Anesthetics, Inhalation; Desflurane; Sevoflurane
• Other Study ID Numbers: EC/12/20/1763

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No