ABSTRACT
Elderly patients coming for orthopaedic surgeries usually have many comorbidities. This makes them potentially vulnerable to haemodynamic instability with a conventional bolus dose of spinal anaesthetic. Fractionating the spinal dose was reported to have haemodynamic stability with a longer duration. Here, we present five cases of high-risk elderly patients with multiple comorbidities who presented for orthopaedic surgeries and were successfully managed with fractional spinal anaesthesia.
Keywords: Dose fractionation, haemodynamic stability, hypotension, spinal anaesthesia, fractional spinal anaesthesia
INTRODUCTION
The elderly population presents a great challenge to anaesthesiologists because of the multiple associated comorbidities, frailty and decreased cognitive reserve with a greater risk for perioperative adverse outcomes. Spinal anaesthesia (SA) is the most used anaesthetic technique for lower limb surgeries. The precipitous hypotension from sympathectomy with a conventional bolus dose for SA is poorly tolerated by frail elderly. Fractionating the conventional spinal dose has recently been reported to have better haemodynamic stability in SA.[1,2] We hypothesised that fractionating the spinal dose will offer better haemodynamic stability in high-risk cases. Here, we present the successful anaesthetic management of five elderly high-risk patients of American Society of Anesthesiologists (ASA) physical status III-IV who presented for orthopaedic lower limb surgeries by fractional spinal anaesthesia (FSA) from July to September 2022 after taking informed consent from them for publication of the case reports.
CASE DESCRIPTION
Case 1
A 75-year-old female, who was hypertensive, diabetic, with parkinsonism and on irregular medication, presented with a fracture neck of the femur following a fall due to syncope and chest pain. On evaluation, her electrocardiogram (ECG) showed non-ST elevation myocardial infarction (NSTEMI). So, she was heparinised and started on dual antiplatelets. Other investigations revealed a deranged renal function and anaemia. Her echocardiography showed concentric left ventricular (LV) hypertrophy and an ejection fraction (EF) of 50%. Cardiology and nephrology evaluation was done. Her hypertension and diabetes were controlled and stabilised on medications, and she was scheduled for hemiarthroplasty 1 week later. We managed this elderly with FSA. The perioperative period was uneventful, without any fresh ECG changes or troponin rise.
Case 2
A 90-year-old man with femur trochanteric fracture who was a known comorbidities. This had a history of aortic stenosis with biprosthetic valve replacement, with grade 2 dyspnoea on exertion (DOE). His pulse rate (PR) was 78 beats/min with atrial fibrillation (AF), and ECG showed AF with no ST–T changes. Echocardiography revealed biprosthetic valve with a maximum atrioventricular AV pressure gradient of 34 mmHg (average 20 mmHg), concentric LV hypertrophy with LV diastolic dysfunction, pulmonary arterial hypertension (PAH) grade 2 and mild mitral regurgitation (MR).
Case 3
A 70-year-old man with a fracture neck of the femur was scheduled for hemiarthroplasty. He was a known case of valvular heart disease with grade 2 DOE and was hypertensive on irregular medications. His baseline PR was 89 beats/min, blood pressure (BP) was 200/120 mmHg and haemoglobin was 9 g/dl. Echocardiography showed rheumatic heart disease – moderate mitral stenosis (valve area 1 cm2) with moderate PAH and MR with the dilated left atrium. The patient was given analgesia with a femoral nerve block, paracetamol 1 g intravenous (IV) infusion, sedation with midazolam 0.5 mg IV, and dexmedetomidine 0.5 μg/kg IV over 15 min. The patient was stabilised and taken up for surgery after a few hours.
Case 4
An 80-year-old man, a chronic smoker, hypertensive and with coronary artery disease, presented with a femur fracture. He also had a cerebrovascular accident 1 month before and was now showing residual hemiparesis on the left side. His PR was 70 beats/min, BP was 180/100 mmHg and bilateral basal crackles in the chest. ECG showed right bundle branch block and T inversion in V1–V6. Echocardiography revealed a patent foramen ovale with left-right L–R shunt, moderate LV dysfunction, PAH, and dilated inferior vena cava. Serum troponin I was positive. After the risk–benefit analysis of regional and general anaesthesia and discussion with relatives, the decision to proceed with FSA was taken.
Case 5
A 78-year-old man, hypertensive with grade 2 DOE and asthmatic on regular medication, was scheduled for femur fracture fixation. He had an active respiratory infection with bilateral bronchospasm and room air oxygen saturation of 86%. His BP was 190/100 mmHg, and PR was 126 beats/min, and he had a systolic murmur at the aortic area. Echocardiography showed aortic sclerosis with a valve area of 1 cm2, global LV dysfunction with an EF of 50% and pulmonary artery pressure of 42 mm H2O. The D-dimer level was not elevated. The patient was optimised with nebulisation and supplemental oxygen.
All these high-risk cases were managed by FSA using 0.5% hyperbaric bupivacaine (7.5–10 mg) with 20 μg of fentanyl. The spinal drug was administered in fractions (two-thirds of the initial drug volume and one-third after 90 s), except for the second case. For the second case, the drug volume was given in three fractions, each with a gap of 45 s. None of the patients had significant haemodynamic changes with FSA intraoperatively [Table 1 and Figure 1] or any untoward perioperative events.
Table 1.
Haemodynamic parameters
| Time | Case 1 | Case 2 | Case 3 | Case 4 | Case 5 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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| HR | SBP | DBP | HR | SBP | DBP | HR | SBP | DBP | HR | SBP | DBP | HR | SBP | DBP | |
| On arrival | 84 | 150 | 90 | 78 | 140 | 80 | 89 | 200 | 120 | 70 | 180 | 100 | 126 | 190 | 100 |
| 0 min (just before spinal) | 82 | 148 | 84 | 72 | 132 | 76 | 62 | 170 | 106 | 74 | 160 | 98 | 118 | 165 | 96 |
| 1 min | 78 | 132 | 80 | 74 | 122 | 70 | 64 | 150 | 100 | 79 | 140 | 86 | 110 | 140 | 90 |
| 3 min | 74 | 130 | 70 | 69 | 118 | 66 | 72 | 130 | 98 | 78 | 122 | 80 | 108 | 120 | 76 |
| 5 min | 72 | 120 | 72 | 70 | 100 | 64 | 75 | 92b | 60 | 72 | 118 | 78 | 109 | 106 | 66 |
| 10 min | 76 | 118 | 78 | 97 | 90a | 60 | 64 | 106 | 70 | 75 | 118 | 78 | 112 | 88a | 70 |
| 15 min | 74 | 114 | 80 | 86 | 106 | 64 | 66 | 118 | 78 | 80 | 120 | 74 | 96 | 100 | 78 |
| 20 min | 80 | 118 | 82 | 76 | 110 | 70 | 70 | 120 | 80 | 74 | 122 | 70 | 99 | 116 | 80 |
| 25 min | 82 | 110 | 74 | 74 | 114 | 70 | 68 | 118 | 86 | 78 | 118 | 68 | 99 | 118 | 82 |
| 30 min | 80 | 120 | 72 | 73 | 110 | 72 | 70 | 110 | 80 | 80 | 118 | 74 | 96 | 124 | 88 |
| 35 min | 78 | 120 | 78 | 75 | 114 | 68 | 74 | 118 | 88 | 82 | 120 | 80 | 92 | 120 | 86 |
| 40 min | 76 | 120 | 70 | 76 | 118 | 72 | 72 | 120 | 90 | 77 | 126 | 82 | 90 | 126 | 90 |
| 45 min | 88 | 124 | 68 | 78 | 110 | 70 | 74 | 126 | 90 | 72 | 128 | 88 | 90 | 130 | 90 |
| 50 min | 82 | 118 | 70 | 76 | 110 | 68 | 73 | 130 | 86 | 94 | 128 | 84 | |||
| 55 min | 78 | 120 | 66 | 77 | 118 | 70 | 76 | 128 | 90 | 90 | 136 | 88 | |||
| 60 min | 79 | 124 | 70 | 80 | 116 | 66 | 70 | 130 | 90 | ||||||
| 65 min | 78 | 128 | 72 | ||||||||||||
| 70 min | 76 | 120 | 74 | ||||||||||||
| 75 min | 78 | 120 | 70 | ||||||||||||
DBP=diastolic blood pressure in mmHg, HR=heart rate in beats per minute, IV=intravenous, SBP=systolic blood pressure in mmHg. aResponded to phenylephrine IV single bolus dose of 50 μg. bRequired two bolus doses of phenylephrine 50 μg
Figure 1.

Intraoperative mean arterial pressure changes in the five cases
DISCUSSION
SA has undergone many modifications to eliminate the associated undesirable haemodynamic adverse effects and to make it more clinically useful even in high-risk patients. The addition of opioids like fentanyl, low-volume preferential unilateral blocks and epidural volume expansion are some of these modifications tried. The latest in the list is FSA, a technique of administering the spinal drug in two or more fractions with a time gap of 45–90 s between the fractions.
Bolus dose with conventional SA causes profound hypotension with an average incidence of 15%–33%, which increases with age, crossing 75% in those older than 50[3] and remains high even with low-dose SA in the elderly.[4] The decreased cardiorespiratory reserve with high resting sympathetic and baroreceptor activity and multiple comorbidities in older adults increases perioperative morbidity and mortality. Fractionating the bolus dose in SA is reported to have better haemodynamic stability and denser blockade.[1,2]
As elderly high-risk patients with cardiac dysfunction depend on LV end-diastolic volume to maintain their stroke volume and cardiac output, the consequences of sympathectomy with SA will be exaggerated. Diastolic dysfunction and reduced baseline cardiac output with the inability to increase the output after SA are the basis of exaggerated post-spinal hypotension in older adults.[5]
Fractionated dosing was reported to cause longer duration with less hypotension and bradycardia and fewer perioperative complications than bolus dose SA.[2] The injection rate has a significant effect on haemodynamics, and a slower rate of spinal drug administration is reported to reduce significant hypotension.[6,7] The exact mechanism of haemodynamic stability with FSA has yet to be clearly discovered. With fractionating the dosing, a lower initial volume of drug spreads in a lesser area, causing vasodilatation and lesser hypotension as sympathectomy is not rapid as with conventional bolus dosing. The subsequent fractions of the drug act on the same blocked area; therefore, there is no further vasodilatation. The longer duration could be due to the action of a second fractional drug dose on the same blocked area. Low fall incidence in mean arterial pressure requiring vasopressors and prolongation of analgesia were our main observations, like in previous reports.[1,7]
CONCLUSION
Fractionating the bolus dose in SA would result in better haemodynamic stability in elderly high-risk patients.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms from all the patients being reported in this case series. In the form, patients has given his/her consent for clinical information to be reported in the journal. Patients understands that his/her name and initials will not be published and due efforts will be made to conceal identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
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