Научная статья на тему 'Сравнение гемодинамических изменений и потребности в их коррекции при проведении спинальной анестезии женщинам с нормальным артериальным давлением и пациенткам с преэклампсией во время кесарева сечения'

Сравнение гемодинамических изменений и потребности в их коррекции при проведении спинальной анестезии женщинам с нормальным артериальным давлением и пациенткам с преэклампсией во время кесарева сечения Текст научной статьи по специальности «Клиническая медицина»

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спинальная анестезия / гипертензия беременных / субарахноидальная блокада / мефентермин

Аннотация научной статьи по клинической медицине, автор научной работы — К. Чигурупалли, Г. Мадабхаттула, С. Шривастава, Р. Пурохит, Б. Б. Ядав

Введение. Спинальная анестезия (СА) широко используется при кесаревом сечении, однако её безопасность у пациенток с преэклампсией (ПЭ) остаётся недостаточно изученной. В данном исследовании проведена оценка использования субарахноидальной блокады (САБ) у рожениц с преэклампсией во время кесарева сечения. Пациенты и методы. В одноцентровое контролируемое клиническое исследование включено 30 беременных женщин с нормальным артериальным давлением и 30 женщин с ПЭ, которым проводилось кесарево сечение. Частоту сердечных сокращений (ЧСС), систолическое артериальное давление (САД), диастолическое артериальное давление (ДАД), среднее артериальное давление (СрАД) и SpO2 оценивали через 1, 3, 5, 7, 9, 11, 13, 15, 20, 25, 30, 40, 45, 50, 55 и 60 минут после начала САБ. Для статистического анализа использовался t-критерий для независимых выборок. Результаты. При сравнении группы пациенток с нормотензией и группы с ПЭ были отмечены статистически значимые различия в массе тела, САД, ДАД и СрАД, причём более высокие значения наблюдались в группе женщин с ПЭ (р<0,05). ЧСС и насыщение крови кислородом были сопоставимыми. Потребность во введении мефентермина была значительно выше у женщин с исходно нормальным артериальным давлением по сравнению с женщинами с ПЭ (p<0,001). Заключение. У женщин с тяжёлой ПЭ при проведении кесарева сечения с использованием САБ наблюдаются значительно более высокие значения САД, ДАД и СрАД по сравнению с женщинами с исходно нормальным артериальным давлением. На ЧСС и насыщение крови кислородом САБ не влияет. Гипотония после спинальной анестезии у пациенток с тяжёлой ПЭ встречается реже, что указывает на потенциальную безопасность СА в данной клинической группе.

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Текст научной работы на тему «Сравнение гемодинамических изменений и потребности в их коррекции при проведении спинальной анестезии женщинам с нормальным артериальным давлением и пациенткам с преэклампсией во время кесарева сечения»

... , , DOI: 10.32415/jsdentia 2023 9 6 42-52

Original article - edn: Yvfrfi

COMPARISON OF HEMODYNAMIC CHANGES AND THEIR MANAGEMENT FOLLOWING SUBARACHNOID BLOCK BETWEEN NORMOTENSIVE AND PREECLAMPTIC WOMEN UNDERGOING CESAREAN SECTION

K. Chigurupalli © 1, G. Madabhattula © 2, S. Srivastava 1, R. Purohit 3, U. Rani © 2, B. B. Yadav 1 D. Kalidindi 2, S. S. Kintali 2, G. Gehlot 3

1 Ananta Institute of Medical Sciences and Research Centre, Kaliwas, India

2 King George hospital, Andhra Medical College, Visakhapatnam, India

3 Geetanjali medical college & hospital, Udaipur, India

H Chigurupalli Kiran — kiran.doc2010@gmail.com

INTRODUCTION. Spinal anesthesia (SA) is widely used for cesarean sections, yet its safety in preeclamptic patients remains uncertain. This study explores the use of subarachnoid block (SAB) in preeclamptic parturients during cesarean sections.

PATIENTS AND METHODS. This study was a single-center hospital-based controlled clinical trial. 30 normotensive and 30 preeclamptic women undergoing cesarean section were included in the study. Heart rate, systolic blood pressure (SBP), diastolic blood pressure (DBP), mean arterial blood pressure (MAP) and SpO2 were evaluated at one, three, five, seven, nine, 11, 13, 15, 20, 25, 30, 40, 45, 50, 55 and 60 minutes intervals after giving the block. The independent samples t-test was used for statistical analysis. RESULTS. In the normotensive (group N) vs. preeclamptic (group PE) comparison, significant differences in weight, SBP, DBP, and MAP were noted, with higher values in group PE (p<0.05). Heart rates and oxygen saturation were comparable. Mephentermine consumption was notably higher in normotensive women compared to preeclamptic women (p<0.001).

CONCLUSION. Severe preeclamptic women exhibit significantly higher SBP, DBP, and MAP compared to normotensive women undergoing cesarean section following subarachnoid block. However, SAB does not impact heart rate and oxygen saturation. Importantly, hypotension following spinal anesthesia is less common in severe preeclamptic patients, indicating its potential safety in this group.

KEYWORDS: Spinal anesthesia, Pregnancy-induced hypertension, Subarachnoid block, Mephentermine.

FOR CITATION: Chigurupalli K, Madabhattula G, Srivastava S, Purohit R, Rani U, Yadav BB, Kalidindi D, Kin-tali SS, Gehlot G. Comparison of Hemodynamic Changes and Their Management Following Subarachnoid Block Between Normotensive and Preeclamptic Women Undergoing Cesarean Section. Juvenis scientia. 2023;9(6):42-52. DOI: 10.32415/jscientia_2023_9_6_42-52.

This article is licensed under a Creative Commons Attribution 4.0 International License. *—*

DOI: 10.32415/jsdentia 2023 9 6 42-52

Оригинальноеисследование - edn: Yvfrfi

СРАВНЕНИЕ ГЕМОДИНАМИЧЕСКИХ ИЗМЕНЕНИИ И ПОТРЕБНОСТИ В ИХ КОРРЕКЦИИ ПРИ ПРОВЕДЕНИИ СПИНАЛЬНОЙ АНЕСТЕЗИИ ЖЕНЩИНАМ С НОРМАЛЬНЫМ АРТЕРИАЛЬНЫМ ДАВЛЕНИЕМ И ПАЦИЕНТКАМ С ПРЕЭКЛАМПСИЕЙ ВО ВРЕМЯ КЕСАРЕВА СЕЧЕНИЯ

К. Чигурупалли © 1, Г. Мадабхаттула 2, С. Шривастава 1, Р. Пурохит 3, У. Рани © 2, Б. Б. Ядав 1, Д. Калидинди © 2, С. С. Кинтали 2, Г. Гехлот 3

1 Институт медицинских наук и исследовательский центр Ананта, Каливас, Индия

2 Больница Короля Георга, Медицинский колледж Андхра, Висакхапатнам, Индия

3 Медицинский колледж и больница Гитанджали, Удайпур, Индия

И Чигурупалли Киран — kiran.doc2010@gmail.com

введение. Спинальная анестезия (СА) широко используется при кесаревом сечении, однако её безопасность у пациенток с преэклампсией (ПЭ) остаётся недостаточно изученной. В данном исследовании проведена оценка использования субарахноидальной блокады (САБ) у рожениц с преэклампсией во время кесарева сечения.

пациенты и методы. В одноцентровое контролируемое клиническое исследование включено 30 беременных женщин с нормальным артериальным давлением и 30 женщин с ПЭ, которым проводилось кесарево сечение. Частоту сердечных сокращений (ЧСС), систолическое артериальное давление (САД), диастолическое артериальное давление (ДАД), среднее артериальное давление (СрАД) и SpO2 оценивали через 1, 3, 5, 7, 9, 11, 13, 15, 20, 25, 30, 40, 45, 50, 55 и 60 минут после начала САБ. Для статистического анализа использовался t-критерий для независимых выборок. результаты. При сравнении группы пациенток с нормотензией и группы с ПЭ были отмечены статистически значимые различия в массе тела, САД, ДАД и СрАД, причём более высокие значения наблюдались в группе женщин с ПЭ (р<0,05). ЧСС и насыщение крови кислородом были сопоставимыми. Потребность во введении мефентермина была значительно выше у женщин с исходно нормальным артериальным давлением по сравнению с женщинами с ПЭ (p<0,001). заключение. У женщин с тяжёлой ПЭ при проведении кесарева сечения с использованием САБ наблюдаются значительно более высокие значения САД, ДАД и СрАД по сравнению с женщинами с исходно нормальным артериальным давлением. На ЧСС и насыщение крови кислородом САБ не влияет. Гипотония после спинальной анестезии у пациенток с тяжёлой ПЭ встречается реже, что указывает на потенциальную безопасность СА в данной клинической группе.

ключевые слова: спинальная анестезия, гипертензия беременных, субарахноидальная блокада, мефентермин.

для цитирования: Чигурупалли К., Мадабхаттула Г., Шривастава С., Пурохит Р., Рани У., Ядав Б.Б., Калидинди Д., Кинтали С.С., Гехлот Г. Сравнение гемодинамических изменений и потребности в их коррекции при проведении спинальной анестезии женщинам с нормальным артериальным давлением и пациенткам с преэклампсией во время кесарева сечения // Juvenis scientia. 2023. Том 9. № 6. С. 42-52. DOI: 10.32415/jscientia_2023_9_6_42-52. EDN: YVFRFI.

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Эта статья доступна по лицензии Creative Commons «Attribution» («Атрибуция») 4.0 Всемирная. h^^^HlH

INTRODUCTION

Spinal anesthesia (SA) or subarachnoid block (SAB) is a form of regional anesthesia and a kind of neuraxi-al block involving injection of opiods, local anesthetics or other permissive drug into the subarachnoid space. Spinal anesthesia offers many advantages for operation although the extent of its benefit is not agreed universally. It has a very rapid onset and provides a dense neural block which can produce highly effective pain relief for a wide variety of indications and may decrease patient morbidity after major surgery, moreover, failures are very infrequent [1, 2].

Advantages of spinal anesthesia include: easy technique, rapid onset, simple performance, requirement of minimum equipments and monitors, little effects on blood biochemistry, optimum levels of arterial blood gases, conscious patients during surgery and maintenance of airway patency, less postoperative care and optimum anesthesia [3].

Pregnancy-induced hypertension (PIH) constitutes major cause of morbidity and mortality in developing countries, and it accompanies 5-10% of all pregnancies [4, 5].

It is postulated that there is a functional imbalance between the endogenous vasodilators (prostacyclin, PG I2) and vasoconstrictors (thromboxane A2) leading to arteriolar vasospasm. There is intense vasoconstriction leading to hypoperfusion of vital organs. The hemodynamic profile is thus altered. Various cardiovascular (CVS) effects like labile blood pressure (BP), decreased colloid oncotic pressure, intravascular volume depletion, increased systemic vascular resistance, hypertension, and hypercoagulable states can coexist. The deleterious effects on central nervous system include cortical blindness, cerebral edema, seizures and cerebrovascular accidents. Renal system involvement can manifest as proteinuria, decrease in renal blood flow with decreased glomerular filtration rate, increased blood urea nitrogen and creatinine. Elevated liver enzymes and decreased plasma serum cholinesterase levels reflect liver involvement. Airway edema, pulmonary edema, and ventilation perfusion mismatch may be associated as a result of respiratory system involvement. Fetal compromise results as a consequence of uteroplacental insufficiency, placental abruption, chronic fetal hypoxia, intrauterine

growth retardation (IUGR), and premature labor and delivery. The definitive cure of PIH is the delivery of fetus and placenta. Termination of pregnancy may be required in the form of induction of labor or cesarean section (CS), which may be a planned or an emergent procedure. Anesthesiologist comes into the picture when cesarean delivery is contemplated. CS may be indicated either in maternal or in fetal interest. The maternal indications may be uncontrolled BP, unfavorable cervix, failed induction of labor, or antepartum hemorrhage [9].

However, anesthesia for cesarean section in a patient with preeclampsia is far more complicated than in an otherwise normal pregnancy for several reasons. Apart from the risks of high incidence of intrauterine growth restriction, fetal distress and prematurity, there are risk of increased perioperative morbidity due to altered hemodynamics in these patients [711]. Either of the two techniques — general anesthesia (GA) or central neuraxial blockade (CNB) — may be employed for anesthesia [6]. Regional anesthesia is often considered to be a safer option in obstetric cases, as the hazards of difficult airway associated with weight gain and edema can be avoided. The technique of anesthesia has to be chosen judiciously based on individual patient condition [6].

Spinal anesthesia seems to be well-suited for in patients undergoing cesarean section because of the short interval from injection to surgical anesthesia [12].

However, spinal anesthesia has not yet been popular due to the common belief that the sudden and extensive sympathetic blockade following subarachnoid block (SAB) will result in severe hypotension that will endanger maternal and fetal safety. Recently, some studies challenged this view and suggested that SAB may in fact be an appropriate choice in preeclamptic women [13, 14].

The ideal technique for anesthesia has been a long controversy among the obstetric anesthesiologists as the risk of hypotension and altered hemodynamics has influenced the choice of anesthesia [7].

The analysis of anesthesia-related deaths during obstetric delivery in the United States from 1979-1990 indicated that general anesthesia is related to 16.7 times increased mortality risk compared with neuraxial blockade for cesarean delivery [15].

Advances in anesthesia drugs and techniques reduced that figure to 1.7 times in between 1979 and 2002, [16] but still more favourable outcomes are found with neuraxial anesthesia. Less morbidity and mortality, less failure, dense anesthesia, easy technique, provision of adequate operating conditions in a shorter time and several other advantages have placed neuraxial anesthesia, particularly, subarachnoid block, as a more preferable mode of anesthesia for elective cesarean section to epidural block or general anesthesia [7].

Recently, some studies have challenged this view and suggested that SAB may in fact be an appropriate choice in preeclamptic women. Yet, this evidence is based on the very few published information regarding the use of SAB in preeclamptic patients [13, 14]. This prompted us to validate the safety of SAB in pre-eclamptic parturients undergoing LSCS.

AIMS AND OBJECTIVES

Aim. This study was aimed to evaluate the hemo-dynamic changes, their management and fetal outcomes following spinal anesthesia between normo-tensive and severe preeclamptic pregnant women undergoing cesarean section.

Objectives:

The objectives of this study were:

1. To compare the hemodynamic changes following subarachnoid block between normotensive and severe preclamptic women undergoing cesarean section.

2. To assess the dosage of mephentermine required to maintain the hemodynamic stability after subarachnoid block in cesarean section.

METHODOLOGY

The present study was conducted in the Department of Anesthesiology, King George Medical College and Hospital, Visakapatnam, India.

Study design. This study was a single-center hospital-based controlled clinical trial.

Study Period. The present study was conducted during the period from January 2021 to October 2022.

Source of Data. Normotensive pregnant women and pregnant women with severe preeclampsia posted for cesarean section under spinal anesthe-

sia under the Department of Anesthesiology, King George Medical College and Hospital, Visakapatnam, Andhra Pradesh were enrolled.

Sample size and sampling procedure. A total of 60 pregnant women that is 30 normotensive and 30 severe preeclamptic women were studied.

The sample size was determined using a desired power of 0.8 and an error of 0.05. Hence, Za was 0.1 i.e. 1.96, Zß was 0.3 i.e. 0.84. The sample size was determined using the following formula.

2(z„+Zß)2*(sD?+SD2)

"" (X1-X2)2

Where,

Z = 1.965 for a=0.05

a

Zß = 0.84 for ß=0.3

5DX = 2.77=3 (Standard deviation for fall in SBP after SAB based on recent study by Mitra M. et al. [7] (2016);

SD2 = 1.28=1(Standard deviation for fall in SBP after SAB based on recent study by Mitra M. et al. [7] (2016);

Xx = 10.39=10 (Mean fall in SBP after SAB based on recent study by Mitra M. et al. [7] (20166);

X2 = 5.01=5 (Mean fall in SBP after SAB based on recent study by Mitra M. et al. [7] (2016).

Hence

2(1.96+U.84)nn(3n+12) n= (iÜS)2

Therefore,

n = 16.50 = 17

the minimum effect size to estimate the effect of SAB on hemodyanamic profile was 17 in each group. However, in order to have uniformity in results and as 60 women were eligible and consented to participate in the study a total sample size of 60 patients divided into two groups of 30 each was considered.

The selected women were divided into two groups of 30 each as below.

Group N: 30 normotensive pregnant women undergoing LSCS.

Group PE: 30 severe preeclamptic pregnant women undergoing LSCS.

Selection Criteria

Inclusion criteria

— Normotensive or severe preclamptic pregnant

women undergoing elective LSCS under spinal anesthesia with ASA Grade I or II

— Women aged between 18 to 30 years and weight 45 to 80 Kg

— Women with singleton pregnancy

Exclusion criteria

— Pregnant women with eclampsia

— Pregnant women with contraindications to subarachnoid block, having local site infection, septicaemia, raised intracranial pressure (ICT)

— Elderly women and obesity (body mass index [BMI] >35 kg/m2)

— Multiple pregnancy

— Pregnant women with cardiac disease, renal disease, diabetes mellitus, coagulopathy and those who refused subarachnoid block

— Pregnant women with placenta praevia, abruptio placenta

Ethical clearance

The study was approved and ethical clearance was obtained from Institutional Ethics Committee, King George Medical College, Visakhapatnam, Andhra Pradesh.

Pre-anesthetic evaluation

A thorough pre-anesthetic evaluation was performed by taking history. In all the patients, height, weight, basal heart rate, respiratory rate and blood pressure were measured and recorded. All parturients were premedicated with oral ranitidine (150 mg) 2 h prior to the surgery. In addition, in severe preeclamptic parturients, antihypertensive medication was continued. After establishing IV access with 18 G cannula prehydration was done with 10 ml/kg body weight of lactated ringer (RL) solution. The volume of administered fluid was not restricted in the severe preeclamptic patients because of the contracted intravascular volume in this group of patients and the high incidence of hypotension caused by spinal anesthesia-induced sympathetic blockade. Standard multichannel monitor was attached and baseline hemodynamic values of various parameters (HR, SBP, DBP, MAP) were recorded. Baseline BP was measured as the mean of the three readings taken 5 min after

arrival in the operation theatre and before doing any invasive procedures.

Anesthesia procedure

All the blocks were perfomed by experienced anesthesiologists. After proper asepsis and draping with betadine, SAB was administered with 25 G spinal needle at L4-5 interspace in sitting posture with 10 mg hyperbaric 0.5% bupivacaine. Infusion of RL was continued at the rate of 5 ml/kg/h. The height of the sensory block was assessed using a pinprick test, and a 10°-15° head down-tilt (Trendelenburg position) was initiated if a T6 sensory level was not achieved at 10 minutes after the spinal injection. Surgery was allowed as soon as upper level of sensory block reached T6. SBP, DBP, MAP, and HR were recorded every 2 min for 15 min and every 5 min thereafter until completion of surgery. Hypotension (defined as MAP < 30% of the baseline) was treated with 6 mg mephentermine IV bolus and the dose was repeated at a 5 min interval if required to maintain MAP within 30% of baseline. Bradycardia (HR < 60 beats/min) if associated with hypotension was treated with 0.6 mg IV atropine (maximum 1.8 mg).

In cases of failed anesthesia or inadequate anesthesia even after 15 minutes general anesthesia was given. No sedation was given to any patients intraoperatively. Oxygen (5 L/min) by facemask was given until delivery of the baby. Fluid therapy was maintained with lactate ringer solution (10 ml/kg/hr).

Outcome variables

Sensory level block

Sensory level was assessed bilaterally with the use of temperature (by cold water swab) and by pin prick at the midclavicular line while motor block was assessed by using Bromage score [17].

— 1 = unable to move feet or knees.

— 2 = able to move feet only.

— 3 = just able to move knees.

— 4 = full flexion of knee and feet

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Hemodynamic monitoring

Heart rate, SBP, DBP, MAP and SpO2 were evaluated at one, three, five, seven, nine, 11, 13, 15, 20, 25, 30, 40, 45, 50, 55 and 60 minutes intervals after giving the block.

Total dose of mephentermine

The total dosage of mephentermine consumed after subarachnoid block was noted.

Statistical Analysis

Data obtained was coded and entered into Microsoft excel spreadsheet. The data was analysed by SPSS statistical software version 20.0. The categorical data was expressed in terms of rates, ratios and percentage and continuous data was expressed as mean ± standard deviation (SD). Chi square test and Fisher's exact test were used to compare the categorical data and continuous data was compared with independent sample t test. A probability value (p value) of less than or equal to 0.05 at 95% confidence interval was considered as statistically significant.

RESULTS

In the present study 66.7% of the women were aged between 26 to 30 years in group N and group PE (p=1.000). Age distribution is presented in Figure 1.

21 to 25 I Group N ■ Group PE

Figure 1. Comparison of age distribution

The comparison of the mean heart rate at different intervals is as shown in Figure 3. It was observed that the mean heart rate was comparable in both the groups at all the intervals (p>0.050).

v ** v

& $ (5s

• Group N # Group PE

Figure 3. Comparsion of heart rate after surgery

The comparison of mean SBP at different intervals is as shown in Figure 4. It was observed that the mean SBP was significantly lower in group N at one minute, three, five, 25, 35, 40, 45, 50, 55 and 60 minutes intervals (p<0.050).

/////////////

~ <s>" ^ ^ ^ # ^ ^ <S>' <fS

1 ^ ^ £

# Group N Q Group PE

Figure 4. Comparsion of systolic blood pressure after surgery

It was observed that the mean age, height, and pulse rate were statistically similar in both the groups (Figure 2). Meanwhile, the weight, SBP, DBP and MAP were significantly higher in group PE (p<0.050).

The comparison of mean DBP at different intervals is as shown in Figure 5. It was observed that the mean DBP was significantly lower in group N at one minute, three, five, and 35 minutes intervals (p<0.050).

Jjjjjj

Age Height Weight Pulse rate SBP (mm DBP (mm MAP (mm (Years) (cm) (kg) (/minute) Hg) Hg) Hg)

I Group N Group PE

Figure 2. Comparison of baseline characteristics

A

.0 .«P .

# Group N # Group PE

Figure 5. Comparsion of diastolic blood pressure after surgery

The comparison of mean MAP at different intervals is as shown in Figure 6. It was observed that the mean MAP was significantly lower in group N at one minute, three, five, 25, 35 and 60 minutes intervals (p<0.050).

120 100

n v v °> ^ ^

# Group N Group PE

Figure 6. Comparison of mean arterial pressure after surgery

The comparison of oxygen saturation at different intervals is as shown in Figure 7. It was observed that the mean oxygen saturation was comparable in both the groups at all the intervals (p>0.050).

sT sT # t®* * >T & J" ф" if № {Г &

N v Л n4 Л rfy <gf

# Group N Group PE

Figure 7. Comparsion of oxygen saturation after surgery

In this study, the consumption of mephentermine (Figure 8) was significantly higher in group N (7.10±5.13 mg) compared to group PE (2.00±3.96 mg) (p<0.001).

Group N Group PE

Figure 8. Comparison of mephentermine requirements

Adverse fetal outcomes were not observed in both studied groups.

DISCUSSION

In the present study, despite of alteration in SBP, DBP and MAP, the mean oxygen saturation was comparable in both the groups at all the intervals (p>0.050). The observed blood pressure values over a continuum does not truly reflect the hemodynamic alteration attributed to physiological changes imparted by SAB in both the groups. The blood pressure values reflect the combined outcome of the physiological effects, ongoing medications and anesthesia management strategy and should be interpreted accordingly [7].

In this study, although significant differences were noted with regard to SBP, DBP and MAP, the mean consumption of mephenterine was significantly higher in normotensive women (7.10±5.13 mg) compared to women with severe preeclampsia (2.00±3.96 mg) (p<0.001). After establishing SAB, blood pressure decreased in both the groups from the baseline, but the minimum SBP, DBP, and MAP recorded during the observation period were always higher in the severe preeclamptic group. The lowest SBP noted among normotensive women was 106.67±15.01 at five minutes interval which gradually increased to 114.37±9.99 mm Hg at 11 minutes interval, gradually decreased to 109.03±10.48 mm Hg at 20 minutes interval and 109.40±10.48 mm Hg at 25 minutes interval. Meanwhile, in women with severe pre-eclampsia the lowest SBP was noted at 20 minutes interval (113.07±16.05 mm Hg) and at nine minutes interval (113.37±13.23 mm Hg). Similarly, the lowest DBP noted among normotensive women was 57.37±9.63 mm Hg at 13 minutes interval while in women with severe preeclampsia the lowest DBP was noted as 59.57±13.33 mm Hg at 20 minutes interval. The lowest SBP, DBP, and significantly lower SBP, DBP and MAP values among normotensive women as discussed above at various intervals resulted in higher vasopressor requirements to treat the episodes of hypotension. These observations suggest that SAB in normotensive women results in hypotension. These observations are similar to a study by Saha D. et al. (2013) who compared the hemodynamic effect and

vasopressor requirement after SAB between normotensive parturients and severe preeclamptic women undergoing cesarean section [5]. After establishing SAB, blood pressure decreased in both the groups from the baseline, but the minimum SBP, DBP, and MAP recorded during the observation period were always higher in the severe preeclamptic group (118.8 ± 6.36, 71.2 ± 12.16, 74.2 ± 7.34, respectively) in comparison with normotensive group (91.9 ± 16.9, 48.76 ± 12.72, 53.7 ± 6.36, respectively), with statistically significant difference (P < 0.0001). Severe preeclamptic patients needed significantly less phenylephrine to treat hypotension (151.1±70 |g in normotensive and 48.3±35.35 |g in severe preeclamptic women), and the difference was statistically significant (p<0.0001). These findings are strong in agreement with the present study.

The present study also corroborates with another study results by Aya et al. (2003), comparing the incidence and severity of hypotension and ephed-rine consumption in 30 preeclamptic women and 30 healthy parturients [18]. They found that SAB-induced hypotension was 6 times less prevalent in preeclamptic women and they required significantly less ephedrine to treat it.

In a study by Dyer et al. (2008) the authors observed the hemodynamic responses to SAB for cesarean delivery in 15 severe preeclamptic parturients and used the beat-to-beat monitoring of cardiac output (CO) for this purpose [19]. The effect to phenylephrine on CO was also observed. They concluded that the changes in CO after SAB in severe preeclamptic women were insignificant, and the reduction in MAP was easily restored by phenylephrine without any decrease in maternal CO.

The findings of the present study are also comparable with a recent study by Mitra M. et al. (2016) where the authors have found significant differences in SBP, DBP and MAP at different points of times in both the groups [7]. One probable explanation of this may be the use of invasive arterial blood pressure monitoring in place of noninvasive monitoring unlike other studies. Also the preoperative blood pressure values were significantly different in both the groups. More phenylephrine consumption was noted in the normotensive group. This indicated higher incidence

of hypotension in the normotensive group and also contributed to the dissimilar magnitude of changes in blood pressure at different points of times. The authors also emphasized on the latter fact as most studies compared different blood pressure values over a point of time with a significant difference in baseline blood pressure values and significant difference in mean vasopressor consumption.

In a normal pregnancy, increased synthesis of endogenous vasodilators like prostaglandins (PGs) and nitric oxide (NO) produces a vasodilated state, and there appears an increased dependence on sympathetic vasoconstriction for control of vascular tone. This explains the sudden and excessive hypotension after sympathetic blockade produced by SAB in them [20]. In preeclampsia, vascular endothelial damage occurs, which produces increased amount of endogenous vasopressors like thromboxane and endothelin that are responsible for maintaining vessel tone. Sympathetic block following SAB does not alter this vascular response, limiting the excessive fall of BP in preeclamptic patients [15, 18].

Visalyaputra et al. (2005) conducted a multicenter randomized study to compare the hemodynamic effects of spinal and epidural anesthesia for cesarean delivery in severely preeclamptic patients and observed in spite of the hypotension (SBP < or + 100 mmHg) being more frequent in the spinal group than the epidural group (51% versus 23%), the duration was short and it was easily treatable with ephedrine [21]. Overall, the present study showed that, despite the significant differences in hemodynamic profiles, especially higher SBP, DBP and MAP, hypotension following spinal anesthesia administered for cesarean section was significantly less common in severe preeclamptic women than in normotensive women as mephentermine requirements were significantly lower in severe preeclamptic parturients. Hence, subarachnoid block in severe preeclamptic patients offers better perioperative hemodynamic stability, less hypotension, less vasopressor consumption and comparable neonatal outcomes. However, these observations require further validation due to potential limitations of this study viz. a single-center study involving a relatively small sample and other associated maternal complications were not consid-

ered. Hence, further multicenter studies involving larger samples and considering other maternal complications may show the pertinent usefulness of SAB in women with severe preeclampsia.

Based on the findings of this study, it may be concluded that there are significant differences in hemodynamic profiles, in particular higher SBP, DBP and MAP, in women with severe preeclampsia compared to normotensive women undergoing cesarean section following subarachnoid block. However, SAB does not alter heart rate and oxygen saturation. At the same time, hypotension following spinal anesthesia ad-

ministered for cesarean section was significantly less common in severe preeclamptic women than in normotensive women as vasopresser requirements were significantly lower in severe preeclamptic parturients.

Funding: The authors declare no funding.

Conflict of interest: The authors declare no conflict of interest.

Author contributions: All authors confirm the authorship according to the international criteria of ICMJE (all authors have made substantial contributions to the conception, design, conduct of the study, and preparation of the manuscript, have read and approved the final version for publication).

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AUTHORS [АВТОРЫ]

И Chigurupalli Kiran, Associate Professor, Department of Radiation Oncology, Ananta Institute of Medical Sciences and Research Centre; ORCID: 0000-0002-9840-7161; email: kiran.doc2010@gmail. com

Madabhattula Girisha, Department of Anesthesiology, King Gorge Hospital, Andhra Medical College; ORCID: 0009-0005-5616-4252

Srivastava Stuti, Associate Professor, Department of Anatomy, Ananta Institute of Medical Sciences and Research Centre; ORCID: 0009-0004-9540-1305

И Чигурупалли Киран, доцент кафедры радиационной онкологии Института медицинских наук и исследовательского центра Ананта; ORCID: 0000-0002-9840-7161; email: kiran.doc2010@gmail. com

Мадабхаттула Гириша, отделение анестезиологии, Больница Короля Георга, Медицинский колледж Андхра; ORCID: 0009-0005-5616-4252

Шривастава Стути, доцент кафедры анатомии Института медицинских наук и исследовательского центра Ананта; ORCID: 0009-0004-9540-1305

Purohit Ramesh, Associate Professor, Department of Radiation Oncology, Geetanjali Medical College & Hospital; ORCID: 0000-0002-5222-292X

Rani Usha, Assistant Professor, Department of Anesthesiology, King Gorge Hospital, Andhra Medical College; ORCID: 0009-0003-1043-9121

Yadav Bhushan Bhratri, Assistant Professor, Department of General Medicine, Ananta Institute of Medical Sciences and Research Centre; ORCID: 00000003-3766-9958

Kalidindi Divyasri, Department of Anesthesiology, King Gorge Hospital, Andhra Medical College; ORCID: 0009-0000-6827-6714

Kintali Sai Santosh, Department of Anesthesiology, King Gorge Hospital, Andhra Medical College; ORCID: 0009-0006-4419-796X

Gehlot Gaurav, Department of Radiation Oncology, Geetanjali Medical College & Hospital; ORCID: 00090001-3315-4511

Пурохит Рамеш, доцент кафедры радиационной онкологии, Медицинский колледж и больница Гитанджали; ORCID: 0000-0002-5222-292X

Рани Уша, доцент кафедры анестезиологии, Больница Короля Георга, Медицинский колледж Андхра; ORCID: 0009-0003-1043-9121

Ядав Бхушан Бхратри, доцент кафедры общей врачебной практики Института медицинских наук и исследовательского центра Ананты; ORCID: 0000-0003-3766-9958

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Калидинди Дивьясри, отделение анестезиологии, Больница Короля Георга, Медицинский колледж Андхра; ORCID: 0009-0000-6827-6714

КинталиСайСантош, отделение анестезиологии, Больница Короля Георга, Медицинский колледж Андхра; ORCID: 0009-0006-4419-796X

Гехлот Гаурав, отделение радиационной онкологии, Медицинский колледж и больница Гитанджал ; ORCID: 0009-0001-3315-4511

Received: 03.04.2023 Accepted: 16.10.2023 Published: 30.12.2023

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