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![]() Open Journal of Obstetrics and Gynecology, 2012, 2, 318-320 OJOG http://dx.doi.org/10.4236/ojog.2012.23066 Published Online September 2012 (http://www.SciRP.org/journal/ojog/) A review of HELLP syndrome, in 17 patients Davut Güven1, Kadir Bakay2*, İdris Koçak1, Cazip Üstün1 1Department of Obstetrics and Gynecology, 19 Mayis University School of Medicine, Samsun, Turkey 2Private Hospital Department of Obstetrics and Gynecology, Turkey Email: *[email protected] Received 15 May 2012; revised 27 June 2012; accepted 9 July 2012 ABSTRACT Introduction: Preeclampsia is a well known obstetric complication characterized with hypertension and proteinuria whereas HELLP syndrome (hemolysis, elevated liver enzymes, low platelet count) which was first stated by Prichard in 1954 and described by Weinstein in 1982, is a multisystemic disease usually seen in the third trimester and in the postpartum period, usually in 48 - 72 hours following delivery [1]. Aim: In this study we aim to share our experience in 17 patients with HELLP syndrome treated in our clinic between January 2005 and March 2008 in re- gard of the current literature. Material and Methods: 17 patients diagnosed with HELLP syndrome between January 2005 and March 2008 were retrospectively re-evaluated in regard of symptoms, treatment op- tions and prognosis. As such this is a retrospective study focusing on case reports. Conclusion: As noted before main focus of treatment should be on patient stability, in other words, palliative care under in- tensive care conditions. Keywords: HELLP; Preeclampsia; Eclampsia; 17 Patients 1. INTRODUCTION Preeclampsia (eclampsia; Greek, “shining forth”) is a well known obstetric complication characterized with hypertension and proteinuria whereas HELLP syndrome (hemolysis, elevated liver enzymes, low platelet count) which was first stated by Prichard in 1954 and described by Weinstein in 1982, is a multisystemic disease usually seen in the third trimester and in the postpartum period, usually in 48 - 72 hours following delivery [1]. With an incidence of 0.2% - 0.8% in all pregnancies and 10% in severe pregnancy its etiology and pathogene- sis is still not fully revealed though it is assumed genetic inheritance, abnormal placentation, immunologic factors and maternal vasculo endothelial dysfunction may play a role [2]. These factors may cause segmental vasospasms and endothelial lesions causing fibrine deposits that result in micro circulatory dysfunctions [3]. Changes described in HELLP syndrome can adversely affect liver and renal functions causing elevated liver enzymes and proteinuria [4]. There are various complications known to be associ- ated with HELLP syndrome, including but not limited to; ascites, pleural effusion, pulmonary edema and dissemi- nated intravascular coagulation (DIC) [1,5,6]. In this study we aim to share our experience in 17 pa- tients with HELLP syndrome that were treated in our clinic between January 2005 and March 2008 in regard of the current literature. Of the 17 cases we have thus reviewed, 3 required in- tensive care management, the remaining 14 recovered in 24 hours after delivery without any complications hence were monitored in the obstetric clinic. 2. AIM In this study we aim to share our clinical experience in 17 patients with HELLP syndrome treated in our clinic between January 2005 and March 2008 in regard of the current literature. We especially aim to present 3 cases who were treated in the intensive care unit to remark treatment options and prognosis in such extreme con- ditions. 3. MATERIAL AND METHODS 17 patients diagnosed with HELLP syndrome between January 2005 and March 2008 were retrospectively re- evaluated in regard of symptoms, treatment options and prognosis. As such this is a retrospective study focusing on case reports. Patients who were treated in intensive care unit are presented in detail as an example of how far the disease could progress and how dramatically it can fully resolve if managed right. 3.1. Case 1 A 25 years old 35 weeks twin pregnancy patient admitted *Corresponding author. OPEN ACCESS ![]() D. Güven et al. / Open Journal of Obstetrics and Gynecology 2 (2012) 318-320 319 to our clinic complaining of headache and nausea. Upon initial examination blood pressure was 170/120 mmHg with ascites and remarkable pretibial edema. In pelvic examination cervix was firm and closed. Ultrasonogra- phy showed two viable fetuses. Initial laboratory results were as follows; Hb: 9.8 g/dl, Hct: 32.9%, Platelets: 177.000, SGOT: 42 IU/l, SGPT: 48 IU/l, proteinuria was present and coagulation parameters were in normal range. Immediate caesarean section was performed and two viable fetuses were delivered. 2 hours following delivery a second laparotomy was deemed necessary due to uncontrollable vaginal bleeding. An increase in liver enzymes and a severe drop in plate- let count were observed right after operation with SGOT: 66 IU/l, SGPT: 81 IU/l and 89.000 respectively. With the appearence of tonic-clonic seizures and se- vere breathing irregularity along with persistant high blood pressure, patient was intubated and transferred to the intensive care unit. While undergoing palliative therapy and close moni- toring a one session of hemodialysis was needed because of anuria and edema. Blood transfusion and fresh frozen plasma had to be administered to stabilize hemodynamic parameters and vascular stability. With the return of renal functions, viable vital signs and normal laboratory results patient was extubated on the 3rd day in intensive care unit. During follow-up no other complications were observed and the patient was discharged 10 days after operation. 3.2. Case 2 A 31 years old 20 weeks pregnancy diagnosed with pre- eclampsia was brought to our clinic after having suffered a tonic-clonic seizure at home. Upon initial examination patient was comatose with a Glascow Coma Score of 9 and blood pressure was 140/90 mmHg, fetal cardiac ac- tivity was absent. Laboratory results were as follows; Hb: 10.9 g/dl, Hct: 34 %, Platelets: 73.000, SGOT: 81 IU/l, SGPT: 67 IU/l and coagulation parameters were in nor- mal range. Immediate caesarean section was performed and the patient transferred to the intensive care unit right after the operation without extubation. MgSO4 therapy was initiated closely monitoring mag- nesium levels and urinary output along with replacement therapy. Hemodialysis was required after stopping MgSO4 due to anuria and edema albeit normal magne- sium levels. After having been intubated for 4 days in the intensive care unit, with continuous monitoring and replacement therapy renal functions returned to normal and liver en- zymes were in a normal range. Patient was transferred back to our clinic after 7 days in the intensive care unit and discharged on the 10th day after operation without any further complications. 3.3. Case 3 A 24 years old 33 weeks pregnancy with a previous his- tory of caesarean section and diagnosed with preeclamp- sia admitted to our clinic complaining of pelvic pain and contractions. Upon initial examination blood pressure was 150/110 mmHg pretibial edema was present. In pel- vic examination cervix was dilated 3 cm with an efface- ment of 70% indicating active labor. Ultrasonography showed one viable fetus. Initial laboratory results were as follows; Hb: 12.8 g/dl, Hct: 36%, Platelets: 141.000, SGOT: 32 IU/l, SGPT: 37 IU/l, proteinuria was present and coagulation parameters were in normal range. Immediate caesarean section was performed and a single viable fetus was delivered. After a rise in blood pressure and liver enzymes along with a decrease in platelet count in the post operative 8th hour, patient was transferred to the intensive care unit for close monitorization. Patient’s renal functions were nor- mal and with palliative therapy vital signs and laboratory results returned to normal range. Patient was transferred back to our clinic after 3 days in the intensive care unit and discharged on the 8th day after operation without any further complications. 4. DISCUSSION HELLP syndrome is diagnosed with hemolysis, elevated liver enzymes and low platelets first stated by Prichard in 1954 and described by Dr. Louis Weinstein in 1982 [1]. In current literature HELLP syndrome is described as a complication usually seen in the early post partum period, up to 6 days, most frequently in the first 48 hours [7]. Of the 3 cases we discussed above, 2 had acute renal failure requiring hemodialysis. Acute renal failure in HELLP syndrome is a very serious complication with an incidence of 7.3% as stated by Sibai [8]. Endothelial damage, vasospasm, platelet activation and a decrease in endothelium derived relaxing factor activity may be blamed for acute renal failure in HELLP syndrome [9]. Whatever the cause, acute renal failure in HELLP syndrome is a serious condition which requires early intervention and intensive care management. Also pa- tients with HELLP syndrome and acute renal failure are more susceptible to other severe complications such as multi organ failure including lungs, brain and heart. Hemolysis in HELLP syndrome can lead to DIC if left unattended therefore it is fairly important to intervene early if such a condition arises. There is no decisive marker to foretell if hemolysis will occur in a preeclamp- Copyright © 2012 SciRes. OPEN ACCESS ![]() D. Güven et al. / Open Journal of Obstetrics and Gynecology 2 (2012) 318-320 Copyright © 2012 SciRes. 320 tic patient but a review of current literature shows Hap- toglobin to be the most sensitive parameter [10]. OPEN ACCESS [6] Sibai, B.M., Taslimi, M.M., EL-Nazer, A., Aman, E., Mabie, B.C. and Ryan, G.M. (1986) Maternal-perinatal outcome associated with the syndrome of hemolysis, elevated liver enzymes, and low platelets in severe pre- eclampsia, eclampsia. American Journal of Obstetrics & Gynecology, 155, 501-509. Even after numerous studies there is still debate on the diagnosis and treatment of HELLP syndrome [11,12]. Main focus should be on palliative care and replacement therapy but as shown in our study hemodialysis might be necessary if renal failure is observed. It is debatable whether or not to administer platelet transfusion to patients with low platelet count to prevent hemorrhage. But transfusion is recommended to patients prior to labor if their platelet count is below 50.000 [13]. Rahman et al. administered steroids to patients with 24 - 34 weeks of pregnancy to further fetal maturation and they observed that when used on patients with HELLP syndrome their platelet count showed a tendency to rise [13]. Also Martin et al. suggested that dexamethasone might benefit patients with a postpartum onset HELLP syn- drome [14]. 5. CONCLUSIONS As noted before main focus of treatment should be on patient stability, in other words, palliative care under intensive care conditions. But more importantly all patients with preeclampsia should be closely monitored both in the antepartum and postpartum period. Awareness in these patients is what saves lives. REFERENCES [1] Weinstein, L. (1982) Syndrome of hemolysis, elevated liver enzymes, and low platelet count: A severe con- sequence of hypertension in pregnancy. American Jour- nal of Obstetrics & Gynecology, 142, 159-167. [2] Sezik, M., Özkaya, M.O., Sezik, H.T., Yapar, E. and Kaya, H. (2005) HELLP sendromlu hastalarda umblikal arter doppler incelemesinin perinatal sonuçlarla ilişkisi. Per- inatoloji Dergisi, 13, 198-202. [3] Loos/Rath (1992) Das HELLP-syndrom-ein “gestaltwan- del der praeklampsie”. Geburtsh. u. Frauenheilk, 52, 581-585. [4] Keleş, G.T., Topçu, İ., Kefi, A., Ekinci, Z. and Sakarya, M. (2006) Yoğun bakım ünitesinde obstetrik olgular. Fırat Tıp Dergisi, 11, 62-65. [5] Weinstein, L. (1985) Preeclampsi/eclampsi with hemoly- sis, ele vated liver enzymes and trombocytopenia. Obstet- rics & Gynecology, 66, 657. [7] Tsoe, E., Reid, R.P., Barish, R.A. and Browne, B.J. (1987) Late past partum eclampsia. Annals of Emergency Me- dicine, 16, 907-909. doi:10.1016/S0196-0644(87)80533-4 [8] Sibai, B.M. and Ramadan, K.M. (1993) Acute renal failure in pregnancies comp licated by hemolysis, ele- vated liver enzymes, ad low platelets. American Journal of Obstetrics & Gynecology, 168, 1682-1690. [9] Sibai, B.M., Villar, M.A. and Mabie, B.C. (1990) Acute renal failure in hypertensi ve disorders: Pregnancy out- come and remote prognosis in thirty-one consecutive cases. American Journal of Obstetrics & Gynecology, 162, 777-783. [10] Kuhn, W., Rath, W., Loos, W. and Graeff, H. (1992) Le syndrome hellp. Resultats cliniques et d’analyse en laboratoire. Rev Fr Gynecol Obstet, 87, 323. [11] Sibai, B.M. (2004) Diagnosis, controversies, and manage- ment of the syndrome of hemolysis, elevated liver en- zymes, and low platelet count. Obstetrics & Gynecology, 103, 981-991. doi:10.1097/01.AOG.0000126245.35811.2a [12] Haddad, B., Barton, J.R., Livingston, J.C., Chahine, R. and Sibai, B.M. (2000) HELLP (hemolysis, elevated liver enzymes, and low platelet count) syndrome versus severe preeclampsia: Onset at< or =28.0 weeks’ gestation. Ame- rican Journal of Obstetrics & Gynecology, 183, 1475- 1479. doi:10.1067/mob.2000.106975 [13] Rahman, T.M. and Wendan, J. (2002) Severe hepatic dysfunction in pregnancy. An International Journal of Medicine, 95, 343-357. [14] Martin, J.N. Jr, Perry, K.G. Jr, Blake, P.G., May, W.A., Moore, A. and Robinette, L. (1997) Beter maternal outcomes are achieved with dexamethasone therapy for postpartum HELLP (hemolysis, elevated liver enzymes and trombocytopenia) syndrome. American Journal of Obstetrics & Gynecology, 177, 1011-1017. doi:10.1016/S0002-9378(97)70005-X ABBREVIATIONS HELLP: hemolysis, elevated liver enzymes, low platelet count; DIC: disseminated intravascular coagulation; MgSO4: magnesium sulphate. |




