Abstract
Pregnancy-induced hypertension constitutes a major cause of morbidity and mortality in developing nations and it complicates about 6–8% of pregnancies. Severe preeclampsia poses a dilemma for the anesthesiologist especially in emergency situations where caesarean deliveries are planned for uninvestigated or partially investigated parturients. This article is aimed to review the literature with regards to the type of anesthesia for such situations. A thorough search of literature was conducted on PubMed, EMBASE, and Google to retrieve the articles. Studies on parturients with severe preeclampsia, undergoing caesarean section, were included in this article. There is growing evidence to support the use of subarachnoid block in such situations when the platelet counts are >80,000 mm-3. Better hemodynamic stability with the use of low-dose local anesthetic along with additives and better neonatal outcomes has been found with the use of subarachnoid block when compared to general anesthesia.
Keywords: Pregnancy-induced hypertension, regional anesthesia or general anesthesia for caesarean deliveries, severe preeclampsia, subarachnoid block for caesarean section, thrombocytopenia and regional anesthesia
Hypertensive disorder during pregnancy can exist in four distinct forms – gestational hypertension, [pregnancy-induced hypertension (PIH)], chronic hypertension, unclassified hypertension, and eclampsia, as classified by the International Society for the Study of Hypertension (ISSHP).[1] PIH complicates around 6–8% of pregnancies. It is a multiorgan disease and is classified as mild PIH or severe PIH. Severe PIH is defined as the presence of systolic blood pressure (SBP) ≥ 160 mmHg and diastolic blood pressure (DBP) ≥ 110 mmHg, on two occasions 6 h apart, associated with proteinuria > 5 g in 24 h, and with evidence of end organ damage.
Pathophysiology
It is postulated that there is a functional imbalance between the endogenous vasodilators (prostacyclins 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 caesarean section (CS), which may be a planned or an emergent procedure. Anesthesiologist comes into the picture when caesarean 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 ante partum hemorrhage. The fetal indications may be fetal distress or IUGR.
Search Strategy
A thorough search of literature was done on the Google search engine, EMBASE, and Pubmed. The articles comparing different techniques of anesthesia for CS in parturients with severe preeclampsia till the year 2010 were included in the study. Studies reflecting upon the hemodynamics and neonatal outcomes with different techniques were included. Recent guidelines on the use of regional anesthesia in patients on anticoagulant therapy were also studied. Studies on mild to moderate preeclampsia were excluded from the review process.
Anesthesia Technique
Either of the two techniques – general anesthesia (GA) or central neuraxial blockade (CNB) – may be employed for anesthesia. GA is often considered unsafe in obstetric practice as such, more so in patients with PIH, because of potentially difficult airway or risk of failed intubation,[2] hypertensive response to laryngoscopy and intubation, risk of aspiration pneumonitis, drug interactions between magnesium and nondepolarizing muscle relaxants (NDMRs) leading to enhanced sensitivity to NDMRs,[3] and impaired villous blood supply.[4]
Regional anesthesia is often considered to be a safer option in such situations 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.
Concern of Severe Hypotension
Often the concern of severe hypotension following subarachnoid block (SAB) deters the anesthesiologist from choosing this technique in patients with severe preeclampsia. A number of studies have been conducted to find the hemodynamic effects of regional anesthesia in patients with preeclampsia. Aya et al. observed that the risk of hypotension was almost six times less in patients with severe preeclampsia than in healthy parturients.[5] Another study, conducted in 2005, attributed the hypotension following SAB to preeclampsia-associated factors, rather than a small uterine mass.[6] A review by Dyer et al. found that preeclampsia patients had a lower susceptibility to hypotension and probably less impairment of cardiac output than healthy parturients after SAB for CS.[7] GA, as well as regional anesthesia, has been shown to be acceptable and safe method for conducting caesarean deliveries in preeclampsia, if steps are taken to ensure a careful approach to either technique.[8] Comparable hemodynamics were observed with use of SAB, GA, or epidural anesthesia (EA), in patients with severe PIH.[9,10] EA has been found to be superior to GA as it is associated with a smaller maternal hemodynamic and neuroendocrine stress response.[11] It reduces the mean arterial pressure (MAP) without altering cardiac index (CI), peripheral vascular resistance (PVR), central venous pressure (CVP), or pulmonary capillary wedge pressure (PCWP).[12] It also offers the advantage of increasing intervillous blood flow provided that adequate preloading is done and supine hypotension is avoided.[12] EA has been traditionally regarded as safer in patients with preeclampsia as compared to SAB as it does not produce sudden hypotension. Recent studies have, however, shown that the reduction in BP is comparable with either of the two techniques.[13–17] Besides maintaining comparable hemodynamics, SAB has the additional advantage of simplicity, faster onset, reliability, and it saves a lot of time.[17] Recently in a prospective observational study on 15 parturients with severe preeclampsia, even SAB has been shown to produce clinically insignificant changes in cardiac output.[18] The hemodynamic alterations produced by SAB are comparable with that in GA in severe preeclampsia[19,20] and hence the uteroplacental blood flow is not altered in parturients receiving SAB.[20]
Opioids have been used by several workers as an additive to local anesthetic for regional anesthesia, thereby reducing the dose of local anesthetic for CS. Better hemodynamic stability with adequate anesthesia has been found with the use of low-dose hyperbaric bupivacaine (7.5–12 mg and as low as 6 mg, 0.5%) and opioid such as fentanyl or sufentanyl as compared to conventional doses of hyperbaric bupivacaine (12.5–13.5 mg, 0.5%).[21,22] Parturients with severe preeclampsia have been successfully managed using an ultra-low dose of intrathecal hyperbaric bupivacaine (3.75 mg, 0.5%) with fentanyl (25 µg) or morphine (100 µg) and diluting with normal saline to make the volume up to 3 ml and 3 ml lidocaine 1.5% given via epidural space. Stable hemodynamics have been reported, obviating the need for vasopressors and large volume preload, minimizing the risk of pulmonary edema due to excessive hydration.[23]
Preloading with crystalloid or colloid in normal parturients undergoing SAB for elective CS has not always been found to be effective.[24,25] Preloading and coloading is still recommended in patients receiving SAB. ASA task force recommends intravenous fluid preloading to decrease the frequency of maternal hypotension in patients undergoing CS under SAB.[26] Preloading is all the more important in PIH patients as hypovolemia and vasospasm are present. Such patients do not require more volume preloads than normotensive controls to prevent catastrophic hypotension under SAB although individual patient variations may be there.[5] About 10 ml/kg fluid should be used to preload the PIH parturients over a period of 10–15 min at the time of SAB.[27]
Ephedrine has been used safely for maintaining BP because it does not adversely affect the uterine blood flow.[28,29] Berends et al. have concluded that the use of prophylactic ephedrine is a safe and effective method for prevention and treatment of hypotension after CSE technique.[29] In a recent study, the degree of hypotension and requirement of vasopressors was found to be similar in two groups of patients administered either SAB or EA.[14] In a prospective study, Sharwood-Smith et al. concluded that patients with severe preeclampsia administered SAB required less ephedrine as compared to those administered EA.[30]
A prospective randomized multicenter study comparing the hemodynamic effects of SAB and EA for CS in preeclampsia showed that although the incidence of hypotension was more frequent in SAB than in the EA group (51% vs. 23%), the duration of significant hypotension (SBP ≤ 100 mmHg) was short (≤1 min) in both the groups. Hypotension was easily treated in both groups by administration of ephedrine, although its use was more in the SAB group. This study concluded that SAB was safe for CS in patients with severe preeclampsia.[15]
Phenylepherine also restores the MAP without increasing the maternal cardiac output.[18] Chiu performed a 5-year retrospective analysis for CS for mild to moderate and severe preeclampsia and found that decreases in BP were similar after SAB and EA. The use of intravenous fluids and ephedrine was also comparable in the two groups. The results support the safety of SAB in women with preeclampsia.[16] Phenylepherine and ephedrine have been compared in a number of studies, which have concluded that neonates of women receiving phenylepherine have higher umbilical artery pH values.[31] A study by Macarthur et al. found that though the uterine artery resistance may be increased with phenylepherine, the oxygen consumption by the fetus is not and, therefore, the net oxygen balance is more favorable with phenylepherine than with ephedrine.[32] ASA task force recommends that both intravenous ephedrine and phenylepherine are acceptable drugs for treating hypotension during neuraxial anesthesia.[26]
Concern Regarding Neonatal Outcomes
Neonatal outcomes after various anesthesia techniques have been studied by various workers. Neonatal APGAR scores and umbilical arterial blood markers are predictors of neonatal outcomes. It has been shown that these variables are not influenced by the type of anesthesia. No statistically significant difference was found in the 1st and 5th minute APGAR scores and umbilical artery blood gas markers (pH, PCO2, HCO3 - BE) between two group of patients administered SAB or GA.[20] Other studies tend to differ and place SAB on a superior platform to GA. APGAR scores have been found to be marginally better in the SAB group in a study conducted by Van Bogaert et al.[10] Other studies in support of SAB have also shown that transient neonatal depression seen after GA can be avoided by using SAB.[11] Neonatal outcome of patients with PIH for CS under SAB and EA has been found to be comparable.[16,30] Even addition of fentanyl to low-dose bupivacaine has not been found to affect the neonatal outcomes.[22]
Complications
The types of complications associated with SAB are less serious and easily manageable as compared to the more serious nature in GA which may even lead to mortality, the reported mortality being as high as 4.3%.[33] Postoperative complications like nausea, vomiting, and hypertension were found to be higher in patients receiving GA. Besides these, SAB does not expose the mothers to the hazards of GA.[20] In a retrospective observational study of 54 cases of SAB, no complications were reported in mothers with preeclampsia and their fetuses, thus establishing the safety of the technique.[34] A retrospective analysis on the duration of hospital stay was conducted on 1619 women who received GA (n = 582) or neuraxial anesthesia [n = 614 for combined spinal and epidural anesthesia (CSEA) and n = 423 for EA]. It was found that neuraxial anesthesia for CS is associated with a shorter duration of hospital stay as compared to GA.[35]
Thrombocytopenia, Coagulopathy, and Subarachnoid Block
A nagging concern while deciding the type of anesthesia is the presence of thrombocytopenia. Platelet function can also be abnormal in such parturients, besides the decrease in platelet count. Platelet count decreases by 20% during normal pregnancy.[36] This, by and large, is not a contraindication for spinal or epidural placement. Approximately 0.5–1% patients present with platelet count of <1,00,000 mm-3.[37] The overall risk of developing an epidural or spinal hematoma after central neuraxial blockade is 1:1,50,000 to 1:2,20,000.[38] Patients with preeclampsia may have rapidly changing platelet counts and it is important that serial platelet counts be taken instead of relying on a single value.
Thrombocytopenia is seen in preeclampsia patients and this may contraindicate regional anesthesia or analgesia. Platelet count <1,00,000 mm-3 is also not a contraindication for EA as indicated by the results of three retrospective studies.[37,39,40] Robson et al. recommend that EA should not be used if the platelet count is below 80 Χ 109L−1.[41] Beilin et al. conducted a survey and found that most anesthetists would perform an epidural when the platelet count is between 80,000 to 1,00,000 mm-3. However, few were willing to place an epidural catheter in counts below 80,000 mm−3.[42] Bleeding time is not a reliable indicator of clotting abnormality as it does not necessarily reflect the risk of bleeding at other sites[43,44] and it is not prolonged until platelet count falls below 1,00,000 mm−3.[45,46] Thromboelastography (TEG) is a better measure of platelet function as it measures all the phases of coagulation and fibrinolysis.[36] Orlikowsky et al. conducted a study comparing platelet count, TEG parameters, and bleeding time in healthy parturients and those with preeclampsia.There was a strong correlation between platelet count and TEG in thrombocytopenic patients.[47] Aspirin is also known to alter the platelet function significantly. Preeclampsia patients may also be on concurrent aspirin prophylaxis, which has been demonstrated to significantly improve the maternal and perinatal outcome in such patients.[48]
A history of easy bruising or evidence of petechiae or ecchymoses should alert the anesthesiologist, and regional anesthesia should be avoided. A platelet count should be obtained. Single values may be inconclusive, but a rapidly decreasing platelet count should be a red signal. A review by Vandermuelen et al. revealed 61 cases of spinal hematoma out of which 68% occurred in patients with coagulopathy and 75% of all the cases had received EA instead of SAB. Out of the cases conducted under EA, 88% had an epidural catheter inserted and almost 50% of these cases developed epidural hematoma after catheter removal.[38]
If the epidural catheter is placed, a midline approach should be used and assessment of sensory and motor function should be done every 2 h. Immediate evaluation should be done if abnormal blockade or prolonged blockade is suspected. If a patient has an epidural catheter in situ and develops a coagulopathy, the catheter should be removed only after the correction of coagulation status.[38] Immediate evaluation is necessary because if the patient has an epidural hematoma, emergency laminectomy and decompression must be performed within 6–12 h to preserve the neurologic function.[49]
SAB offers an advantage over EA for it can be performed with a smaller gauge needle in contrast to a larger gauge needle required for EA. Koyama et al. have reported a case of spinal subarachnoid hematoma following SAB in a patient with HELLP syndrome. The case was followed up and managed conservatively and the patient had an almost complete recovery within 3 months. They concluded that it is important for the clinicians to recognize the symptoms and signs of spinal subarachnoid hematoma to avoid delay in the treatment that might result in severe neurological deficit.[50]
Single shot SAB May be a good choice for CS when compared to GA or EA even for patients with severe preeclampsia without features of impending eclampsia. Careful selection of patients is, however, important. SAB is safe both for the mother and the baby; it provides better neonatal outcome and has fewer complications. Early breast feeding can be initiated. The shorter duration of hospital stay is an added advantage for the mother and the newborn.
Footnotes
Source of Support: Nil
Conflict of Interest: None declared.
References
- 1.Davey DA, McGillivray I. The classification and definition of Hypertensive disorders of pregnancy. Am J Obstet Gynecol. 1988;158:892–8. doi: 10.1016/0002-9378(88)90090-7. [DOI] [PubMed] [Google Scholar]
- 2.Brimacombe J. Acute pharyngolaryngeal oedema and pre-eclamptic toxaemia. Anesth Inten Care. 1992;20:97–8. doi: 10.1177/0310057X9202000123. [DOI] [PubMed] [Google Scholar]
- 3.Sinatra RS, Philip BK, Naulty JS, Ostheimer GW. Prolonged neuromuscular blockade with vecuronium in a patient treated with magnesium sulfate. Anesth Analg. 1985;64:1220–2. [PubMed] [Google Scholar]
- 4.Jouppila P, Kuikka J, Jouppila R, Hollmén A. Effect of induction of general anaesthesia for caesarean section on intervillous blood flow. Acta Obstet Gynecol Scand. 1979;58:249–53. doi: 10.3109/00016347909154043. [DOI] [PubMed] [Google Scholar]
- 5.Aya AG, Mangin R, Vialles N, Ferrer JM, Robert C, Ripart J, et al. Patients with severe pre-eclampsia experience less hypotension during spinal anaesthesia for caesarean delivery than healthy parturients: A prospective cohort comparison. Anesth Analg. 2003;97:867–72. doi: 10.1213/01.ANE.0000073610.23885.F2. [DOI] [PubMed] [Google Scholar]
- 6.Aya AG, Vialles N, Tanoubi I, Mangin R, Ferrer JM, Robert C, et al. Spinal anaesthesia-induced hypotension: A risk comparison between patients with severe pre-eclampsia and healthy women undergoing preterm caesarean delivery. Anesth Analg. 2005;101:869–75. doi: 10.1213/01.ANE.0000175229.98493.2B. [DOI] [PubMed] [Google Scholar]
- 7.Dyer RA, Piercy JL, Reed AR. The role of the anaesthetist in the management of the pre-eclamptic patient. Curr Opin Anaesthesiol. 2007;20:168–74. doi: 10.1097/ACO.0b013e328136c1ac. [DOI] [PubMed] [Google Scholar]
- 8.Wallace DH, Leveno KJ, Cunningham FG, Giesecke AH, Shearer VE, Sidawi JE. Randomised comparison of general and regional anaesthesia for caesarean delivery in pregnancies complicated by severe preeclampsia. Obstet Gynecol. 1995;86:193–9. doi: 10.1016/0029-7844(95)00139-i. [DOI] [PubMed] [Google Scholar]
- 9.Rout CC, Ward S, Rocke DA. Hemodynamic variability at emergency caesarean section in hypertensive patients: Spinal versus General anaesthesia. Anaesthesia. 1998;(Suppl):A50. 30th annual meeting of the Society for Obstetric Anaesthesia and perinatology (SOAP), Vancouver, B.C. [Google Scholar]
- 10.Van Bogaert LJ. Spinal block caesarean section in parturients with pregnancy induced hypertension. East Afr Med J. 1998;75:227–31. [PubMed] [Google Scholar]
- 11.Ramanathan J, Coleman P, Sibai B. Anesthetic modification of hemodynamic and neuroendocrine stress responses to caesarean delivery in women with severe preeclampsia. Anesth Analg. 1991;73:772–9. doi: 10.1213/00000539-199112000-00016. [DOI] [PubMed] [Google Scholar]
- 12.Newsome LR, Bramwell RS, Curling PE. Severe preeclampsia: Hemodynamic effects of lumbar epidural anaesthesia. Anesth Analg. 1986;65:31–6. [PubMed] [Google Scholar]
- 13.Hood DD, Boese PA. Epidural and spinal anaesthesia for caesarean section in severely pre-eclamptic patients. Reg Anesth. 1992;17:35. [Google Scholar]
- 14.Clark VA, Smith SG, Stewart AV. Ephedrine requirements are reduced during spinal anaesthesia for caesarean section in pre-eclampsia. Int J Obstet Anaesth. 2005;14:9–13. doi: 10.1016/j.ijoa.2004.08.002. [DOI] [PubMed] [Google Scholar]
- 15.Visalyaputra S, Rodanant O, Somboonviboon W, Tantivitayatan K, Thienthong S, Saengchote W. Spinal versus Epidural anaesthesia for caesarean delivery in severe pre-eclampsia: A prospective randomised multicenter study. Anesth Analg. 2005;101:862–8. doi: 10.1213/01.ANE.0000160535.95678.34. [DOI] [PubMed] [Google Scholar]
- 16.Chiu CL, Mansor M, Ng KP, Chan YK. Retrospective review of spinal versus epidural anaesthesia for caesarean section in pre-eclamptic patients. Int J Obstet Anesth. 2003;12:23–7. doi: 10.1016/s0959-289x(02)00137-1. [DOI] [PubMed] [Google Scholar]
- 17.Ishrat HM, Raja AT. Spinal anaesthesia in pre-eclamptic parturient-prospective cohort study. Internet J Anaesthesiol. 2007;14:ISSN1092–406. [Google Scholar]
- 18.Dyer RA, Piercy JL, Reed AR, Lombard CJ, Schoeman LK, James MF. Hemodynamic changes associated with spinal anaesthesia for caesarean delivery in severe pre-eclampsia. Anesthesiology. 2008;108:802–11. doi: 10.1097/01.anes.0000311153.84687.c7. [DOI] [PubMed] [Google Scholar]
- 19.Dyer RA, Els I, Farbas J, Torr GJ, Schoeman LK, James MF. Prospective, randomised trial comparing general with spinal anaesthesia for caesarean delivery in pre-eclamptic patients with a non-reassuring foetal heart trace. Anesthesiology. 2003;99:561–9. doi: 10.1097/00000542-200309000-00010. [DOI] [PubMed] [Google Scholar]
- 20.Moslemi F, Rasooli S. Comparison of spinal versus general anaesthesia for caesarean delivery in patients with severe preeclampsia. J Med Sci. 2007;7:1044–8. [Google Scholar]
- 21.Ramanathan J, Vaddadi AK, Arheart KL. Combined spinal and epidural anaesthesia with low doses of intrathecal bupivacaine in women with severe preeclampsia: A preliminary report. Reg Anesth Pain Med. 2001;26:46–51. doi: 10.1053/rapm.2001.18182. [DOI] [PubMed] [Google Scholar]
- 22.Rasooli S, Parish M, Mahmoodpoor A, Moslemi F, Sanaie S. Effect of spinal low-dose bupivacaine-sufentanyl for caesarean section in pre-eclamptic parturients on neonatal outcome. Shiraz E-Med J. 2009;10:201–8. [Google Scholar]
- 23.Teoh WH, Sia AT. Ultra-low dose combined spinal-epidural anaesthesia for caesarean section in severe pre-eclampsia. Anaesthesia. 2006;61:511–2. doi: 10.1111/j.1365-2044.2006.04630.x. [DOI] [PubMed] [Google Scholar]
- 24.Ueyama H, He YL, Tanigami H, Mashimo T, Yoshiya I. Effects of crystalloid and colloid preload on blood volume in the parturient undergoing spinal anaesthesia for elective caesarean section. Anesthesiology. 1999;91:571–6. doi: 10.1097/00000542-199912000-00006. [DOI] [PubMed] [Google Scholar]
- 25.Rout CC, Rocke DA, Levin J, Gouws E, Reddy D. A reevaluation of the role of crystalloid in the prevention of hypotension associated with spinal anaesthesia for elective caesarean section. Anesthesiology. 1993;79:262–9. doi: 10.1097/00000542-199308000-00011. [DOI] [PubMed] [Google Scholar]
- 26.ASA task force on Obstetric Anaesthesia Practice Guidelines for Obstetric Anaesthesia. 2006 [Google Scholar]
- 27.Mojica JL, Melendez HJ, Bautista LE. The timing of intravenous crystalloid administration and incidence of cardiovascular side-effects during spinal anaesthesia: The results from a randomised controlled trial. Anesth Analg. 2002;94:432–7. doi: 10.1097/00000539-200202000-00039. [DOI] [PubMed] [Google Scholar]
- 28.Cotton DB, Lee W, Huhta JC, Dorman KF. Hemodynamic profile in severe pregnancy induced hypertension. Am J Obstet Gynecol. 1988;158:523–9. doi: 10.1016/0002-9378(88)90017-8. [DOI] [PubMed] [Google Scholar]
- 29.Berends N, Teunkens A, Vandermeersch E, Van de Velde M. A randomised trial comparing low-dose combined spinal-epidural anaesthesia and conventional epidural anaesthesia for caesarean section in severe pre-eclampsia. Acta Anaesthesiol Belg. 2005;56:155–62. [PubMed] [Google Scholar]
- 30.Smith SG, Clark V, Watson E. Regional anaesthesia for caesarean section in severe pre-eclampsia: Spinal anaesthesia is the preferred choice. Int J Obstet Anaesth. 1999;8:85–9. doi: 10.1016/s0959-289x(99)80003-x. [DOI] [PubMed] [Google Scholar]
- 31.Lee A, Ngan Kee WD, Gin T. A quantitative systematic review of randomised controlled trials of ephedrine versus Phenylepherine for the management of hypotension during spinal anaesthesia for caesarean deliveries. Anesth Analg. 2002;94:920–6. doi: 10.1097/00000539-200204000-00028. [DOI] [PubMed] [Google Scholar]
- 32.Macarthur A, Riley ET. Obstetric Anesthesia controversies: Vasopressor choice for post-spinal hypotension during caesarean deliveries. Int Anesthesiol Clin. 2007;45:115–32. doi: 10.1097/AIA.0b013e31802b8d53. [DOI] [PubMed] [Google Scholar]
- 33.Ahmed SM, Khan RM, Bano S, Ajmani P, Kumar A. Is spinal anaesthesia safe in pre-eclamptic patients? J Ind Med Assoc. 1999;97:165–8. [PubMed] [Google Scholar]
- 34.Shifman EM, Filippovich GV. Safety of subarachnoid anaesthesia during caesarean section in pregnant women with pre-eclampsia. Anesteziol Reanimatol. 2003;5:38–41. [PubMed] [Google Scholar]
- 35.Fassoulaki A, Petropoulos G, Staikou C, Siafaka I, Sarantapoulos C. General versus neuraxial anaesthesia for caesarean section: Impact on the duration of hospital stay. J Obstet Gynecol. 2009;29:25–30. doi: 10.1080/01443610802628569. [DOI] [PubMed] [Google Scholar]
- 36.Beilin Y, Abramovitz S. The anticoagulated parturient. Int Anesthesiol Clin. 2007;45:71–81. doi: 10.1097/AIA.0b013e31802b8ad4. [DOI] [PubMed] [Google Scholar]
- 37.Beilin Y, Zahn J, Comerford M. Safe epidural analgesia in 30 parturients with platelet count between 69000 and 98000 cumm-1. Anesth Analg. 1997;85:385–8. doi: 10.1097/00000539-199708000-00025. [DOI] [PubMed] [Google Scholar]
- 38.Vandermeulen EP, Van Aken H, Vermylen J. Anticoagulants and spinal-epidural anaesthesia. Anesth Analg. 1994;79:1165–77. doi: 10.1213/00000539-199412000-00024. [DOI] [PubMed] [Google Scholar]
- 39.Rasmus KT, Rottman RL, Kotelko DM, Wright WC, Stone JJ, Rosenblatt RM. Unrecognised thrombocytopenia and regional anaesthesia in parturients: A retrospective review. Obstet Gynecol. 1989;73:943–6. doi: 10.1097/00006250-198906000-00007. [DOI] [PubMed] [Google Scholar]
- 40.Rolbin SH, Abbott D, Musclow E, Papsin F, Lie LM, Freedman J. Epidural anaesthesia in pregnant patients with low platelet counts. Obstet Gynecol. 1988;71:918–20. [PubMed] [Google Scholar]
- 41.Robson S, Howell P. Report of a Royal College of Obstetrics and Gynecology meeting 1994 on hypertension in pregnancy. Br J Obstet Gynecol. 1994;101:639–44. [Google Scholar]
- 42.Beilin Y, Bodian CA, Haddad EM, Leibowitz AB. Practice patterns of anaesthesiologists regarding situations in obstetric anaesthesia where clinical management is controversial. Anesth Analg. 1996;83:735–41. doi: 10.1097/00000539-199610000-00013. [DOI] [PubMed] [Google Scholar]
- 43.Rodgers RP, Levin J. A critical reappraisal of the bleeding time. Semen Thrombi Hemost. 1990;16:1–20. doi: 10.1055/s-2007-1002658. [DOI] [PubMed] [Google Scholar]
- 44.Lind SE. The bleeding time does not predict surgical bleeding. Blood. 1991;77:2547–52. [PubMed] [Google Scholar]
- 45.Hawkins JL, Konini LM, Palmer SK, Gibbs CP. Anesthesia related deaths during obstetric delivery in the United States 1979-1990. Anesthesiology. 1997;86:277–84. doi: 10.1097/00000542-199702000-00002. [DOI] [PubMed] [Google Scholar]
- 46.Harker LA, Slichter SJ. The bleeding time as a screening test for evaluation of platelet function. New Engl J Med. 1972;287:155–9. doi: 10.1056/NEJM197207272870401. [DOI] [PubMed] [Google Scholar]
- 47.Orlikowski CE, Rocke DA, Murray WB, Gouws E, Moodley J, Kenoyer DG, et al. Thromboelastography changes in pre-eclampsia and eclampsia. Br J Anaesth. 1996;77:157–61. doi: 10.1093/bja/77.2.157. [DOI] [PubMed] [Google Scholar]
- 48.Schiff E, Peleg E, Goldenberg M, Rosenthal T, Ruppin E, Tamarkin M, et al. The use of aspirin to prevent preeclampsia and lower the ratio of Thromboxane A2 to prostacyclins in relatively high risk pregnancies. New Engl J Med. 1989;321:351–6. doi: 10.1056/NEJM198908103210603. [DOI] [PubMed] [Google Scholar]
- 49.Stephanov S, de Preux J. Lumbar epidural hematoma following epidural anaesthesia. Surg Neurol. 1982;18:351–3. doi: 10.1016/0090-3019(82)90149-5. [DOI] [PubMed] [Google Scholar]
- 50.Koyama S, Tomimatsu T, Kanagawa T, Sawada K, Tsutsui T, Kimura T, et al. Spinal subarachnoid hematoma following spinal anesthesia in a patient with HELLP syndrome. Int J Obstet Anesth. 2010;19:87–91. doi: 10.1016/j.ijoa.2009.05.007. [DOI] [PubMed] [Google Scholar]