HELLP Syndrome: Difference between revisions

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<br>[Image courtesy of [http://www.ispub.com/journal/the_internet_journal_of_anesthesiology.html The Internet Journal of Anesthesiology]]
<br>[Image courtesy of [http://www.ispub.com/journal/the_internet_journal_of_anesthesiology.html The Internet Journal of Anesthesiology]]  


== Prevalence  ==
== Prevalence  ==


As of Nov 2010, for every 1,000 pregnancies, 1 to 2 (0.5%-0.9%) women will be diagnosed with HELLP syndrome.&nbsp;&nbsp;Furthermore,&nbsp;10-20% of women diagnosed with severe&nbsp;[http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001900 preeclampsia]&nbsp;will be diagnsosed with HELLP.<ref name="PubMed" /> Mortality rates associated with HELLP syndrome have been reported as high as 25%.<ref name="Padden" />  
As of Nov 2010, for every 1,000 pregnancies, 1 to 2 (0.5%-0.9%) women will be diagnosed with HELLP syndrome.&nbsp;&nbsp;Furthermore,&nbsp;10-20% of women diagnosed with severe&nbsp;[http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001900 preeclampsia]&nbsp;will be diagnosed with HELLP.<ref name="PubMed" /> Mortality rates associated with HELLP syndrome have been reported as high as 25%.<ref name="Padden" />  


Patients have a 19-27% chance of reoccurance on subsequent pregnancies.<ref name="Padden">Padden MO. HELLP Syndrome: Recognition and Perinatal Management. American Family Physician. September 1999. Available online at http://www.aafp.org/afp/990901ap/829.html. Accessed 1 March 2011.</ref>  
Patients have a 19-27% chance of reoccurrence on subsequent pregnancies.<ref name="Padden">Padden MO. HELLP Syndrome: Recognition and Perinatal Management. American Family Physician. September 1999. Available online at http://www.aafp.org/afp/990901ap/829.html. Accessed 1 March 2011.</ref>  


== Characteristics/Clinical Presentation  ==
== Characteristics/Clinical Presentation  ==
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(''Full HELLP syndrome classifications have a higher mortality rate and should be delivered within 48 hours'')  
(''Full HELLP syndrome classifications have a higher mortality rate and should be delivered within 48 hours'')  


*Classification 2:&nbsp;&nbsp;Basis of platlet&nbsp;count
*Classification 2:&nbsp;&nbsp;Basis of platelet&nbsp;count


&nbsp;&nbsp;&nbsp; - Class 1:&nbsp; Platlet count &lt; 50,000 mm<sup>3</sup>  
&nbsp;&nbsp;&nbsp; - Class 1:&nbsp; Platelet count &lt; 50,000 mm<sup>3</sup>  


&nbsp;&nbsp;&nbsp; - Class 2:&nbsp; Platlet count 50,000-100,000 mm<sup>3</sup>  
&nbsp;&nbsp;&nbsp; - Class 2:&nbsp; Platelet count 50,000-100,000 mm<sup>3</sup>  


&nbsp;&nbsp;&nbsp;&nbsp;-&nbsp;Class 3:&nbsp; Platlet count 100,000-150,000 mm<sup>3</sup>  
&nbsp;&nbsp;&nbsp;&nbsp;-&nbsp;Class 3:&nbsp; Platelet count 100,000-150,000 mm<sup>3</sup>  


(''Class 1 pts have a higher maternal morbidity and mortality rate'')  
(''Class 1 pts have a higher maternal morbidity and mortality rate'')  
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== Medications  ==
== Medications  ==


''Maternal Medications<ref name="Padden" />''
''Maternal Medications<ref name="Padden" />''  


*Magnesium sulfate – anticonvulsant to prevent seizures  
*Magnesium sulfate – anticonvulsant to prevent seizures  
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== Systemic Involvement  ==
== Systemic Involvement  ==


HELLP syndrome mainly involves the liver and the blood&nbsp;therefore is part of the digestive and circulatory system as described in the Etiology/Causes section. However, if left untreated muliple organs systems can go into failure as described in the Associated co-morbidities section.&nbsp;  
HELLP syndrome mainly involves the liver and the blood&nbsp;therefore is part of the digestive and circulatory system as described in the Etiology/Causes section. However, if left untreated multiple organs systems can go into failure as described in the Associated co-morbidities section.&nbsp;  


== Medical Management (current best evidence)  ==
== Medical Management (current best evidence)  ==

Revision as of 14:13, 9 March 2011

 

Welcome to PT 635 Pathophysiology of Complex Patient Problems This is a wiki created by and for the students in the School of Physical Therapy at Bellarmine University in Louisville KY. Please do not edit unless you are involved in this project, but please come back in the near future to check out new information!!

Original Editors - Carolyn S. Furdek from Bellarmine University's Pathophysiology of Complex Patient Problems project.

Lead Editors - Your name will be added here if you are a lead editor on this page.  Read more.

Definition/Description[edit | edit source]

File:Liver.jpg
A liver affected by HELLP Syndrome


HELLP syndrome is an acronym for several life-threatening symptoms that occur together in a woman’s pregnancy.

These symptoms are:




[Image courtesy of The Internet Journal of Anesthesiology]

Prevalence[edit | edit source]

As of Nov 2010, for every 1,000 pregnancies, 1 to 2 (0.5%-0.9%) women will be diagnosed with HELLP syndrome.  Furthermore, 10-20% of women diagnosed with severe preeclampsia will be diagnosed with HELLP.[1] Mortality rates associated with HELLP syndrome have been reported as high as 25%.[2]

Patients have a 19-27% chance of reoccurrence on subsequent pregnancies.[2]

Characteristics/Clinical Presentation[edit | edit source]

Approximately 7 out of 10 patients with HELLP syndrome will experience the symptoms prior to delivery between the 27th and 37th week of gestation. The remaining patients will develop the symptoms within 48 hours postpartum.[3]

There are two classifications of HELLP Syndrome:[2]

  • Classification 1:  Basis of 3 classic lab values

    - Partial: one/two of the classic values present 

    - Full:  all three abnormalities present

(Full HELLP syndrome classifications have a higher mortality rate and should be delivered within 48 hours)

  • Classification 2:  Basis of platelet count

    - Class 1:  Platelet count < 50,000 mm3

    - Class 2:  Platelet count 50,000-100,000 mm3

    - Class 3:  Platelet count 100,000-150,000 mm3

(Class 1 pts have a higher maternal morbidity and mortality rate)

Clinical symptoms of HELLP include discomfort in the upper right quadrant of the abdomen, pain in the epigastric area, vomiting, and nausea.[3] The abdominal discomfort can increase and decrease throughout the day.[4] Patients can report extreme fatigue prior to presentation or ‘feeling unwell’.[4][1] Other symptoms include headache, fluid retention, excess weight gain, blurry vision, nosebleeds (or bleeding that does not stop easily), seizures/convulsions.[1]

Associated Co-morbidities[edit | edit source]

HELLP syndrome can lead patients to be at a higher risk for the following conditions:[5][6]

  • Renal Failure - loss of the kidney’s ability to function properly. The body will no longer be capable of filtering excess fluid, waste, and salts from the blood. This leads to dangerous levels in the system.[7]
  • Consumptive coagulopathy  - (also known as disseminated intravascular coagulation (DIC)) - clotting factors reduced[8]
  • Abruptio placentae - the placenta nourishing the fetus abruptly separates from the uterine wall prior to delivering the baby[8]
  • Pulmonary edema - fluid build up in the lungs - can lead to shortness of breath.[8]
  • Cerebral edema - build up of fluid around the brain[9]
  • Subcapsular liver hematoma - pooling of blood just outside of the liver
  • Hypovolemic shock - excessive fluid and blood loss that can lead to organ failure[8]

Medications[edit | edit source]

Maternal Medications[2]

  • Magnesium sulfate – anticonvulsant to prevent seizures
  • Antihypertensive medications – high blood pressure
  • Blood product – if necessary
  • Dexamethasone – corticosteroid used for fetus lung maturity prior to delivery 

Diagnostic Tests/Lab Tests/Lab Values[edit | edit source]

Hemolysis: 

  • Low haptoglobin concentration (< 1 g/L – < 0.4 g/L)  - more specific indicator [3]
  • High LDH[3]
  • presence of unconjugated bilirubin[3]

   (if Hematocrit normal: decreased serum haptoglobin levels may be present indicating HELLP)[2]

Liver Enzymes: As high as 4,000 U per L[2]

Platelets: As low as 6,000 per mm3 (anything less than 150,000 per mm3 should be of concern)[2]

Plasma fibrogen: levels less than 300 mg per dL (DIC suspected)[2] 

Etiology/Causes[edit | edit source]

In 1982 L Weinstein identified cardinal signs and symptoms that were a variant of severe preeclampsia and named the condition HELLP.[10]

The overall cause of HELLP syndrome in pregnant women is unknown at this time. However, researchers do have a better understanding of the three main characteristics that are known to occur with HELLP. These symptoms are: haemolysis, elevation of liver enzymes, and thrombocytopenia.

  • Haemolysis occurs due to microangiopathic haemolytic anaemia (MAHA). Blood smears have shown contracted red cells w/ spicula, polychromatic red cells, and increased reticulocyte counts. All these findings lead researches to suspect the development of MAHA. Increased LDH levels and decreased haemoglobin concentrations further show Haemolysis.[3]
  • Elevated liver enzymes indicates the involvement of the liver as well as reflecting the haemolytic process.[3]
  • Thrombocytopenia has been associated to the destruction of platelets.[2] 


**A recent study out of Turkey (published in March 2011) found that Homocysteine levels were significantly higher and a increased likelihood of deficiency in antithrombin III were found in women diagnosed with HELLP.[11] (Further research in this area is needed in order to validate this report)

Systemic Involvement[edit | edit source]

HELLP syndrome mainly involves the liver and the blood therefore is part of the digestive and circulatory system as described in the Etiology/Causes section. However, if left untreated multiple organs systems can go into failure as described in the Associated co-morbidities section. 

Medical Management (current best evidence)[edit | edit source]

In patients diagnosed with HELLP syndrome prior to delivery, the immediate treatment is delivery of the fetus.[12] If the fetus is earlier than 34 weeks gestation, steroid injections and close monitoring for 24-48 hours may be provided to allow the fetus’ lungs to mature.[3] 

Figure: Suggested protocol in treating pts with HELLP Syndrome

[Chart courtesy of Journal of The American Family Physician: HELLP Syndrome]

Physical Therapy Management (current best evidence)[edit | edit source]

Due to the severity and risk of maternal mortality, conservative management is not recommended in the treatment of HELLP syndrome.[3] 

Alternative/Holistic Management (current best evidence)[edit | edit source]

Due to the severity and risk of maternal mortality, conservative management is not recommended in the treatment of HELLP syndrome.[3] 

Differential Diagnosis[edit | edit source]

HELLP Syndrome my be misdiagnosed as any of the below conditions:[3]

  • Viral Hepatitis
  • Cholangitis
  • Acute fatty liver of pregnancy
  • Haemolytic uremic syndrome
  • Thrombotic thrombocytopenic purpura
  • Systemic lupus erythematosus

Case Reports/ Case Studies[edit | edit source]


Resources
[edit | edit source]

Recent Related Research (from Pubmed)[edit | edit source]

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References[edit | edit source]

  1. 1.0 1.1 1.2 1.3 PubMed Health website. HELLP syndrome. Available at http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001892. Accessed February 18, 2011.
  2. 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 2.8 Padden MO. HELLP Syndrome: Recognition and Perinatal Management. American Family Physician. September 1999. Available online at http://www.aafp.org/afp/990901ap/829.html. Accessed 1 March 2011.
  3. 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 Haram, K. Svendsen, E. Abildgaard, U. The HELLP syndrome: Clinical issues and management. A Review. BMC Pregnancy Childbirth [serial online]. 2009; 9:8.
  4. 4.0 4.1 Sibai BM. Diagnosis, controversies, and management of the syndrome of hemolysis, elevated liver enzymes, and low platelet count. Obstetrics and Gynecology [serial online]. 2004;103:981–991.
  5. Svenningsen R, Morken NH, Kahn JA. Corticosteroids in the treatment of HELLP-syndrome? Tidsskr Nor Laegeforen. 2006;126(17):2253–2256.
  6. Vigil-De Gracia PE, Tenorio-Marañón RF, Cejudo-Carranza E, Helguera-Martinez A, García-Cáceres E. Difference between pre-eclampsia, HELLP syndrome and eclampsia, maternal evaluation. Ginecol Obstet Mex. 1996;64:337–382.
  7. Mayo Clinic web site. Acute Kidney Failure. Available at: http://www.mayoclinic.com/health/kidney-failure/DS00280. Accessed February 22, 2011.
  8. 8.0 8.1 8.2 8.3 Definitions, Online - Medline Plus. Available online at http://www.nlm.nih.gov/medlineplus/. Accessed 1 March 2011.
  9. Definitions, Online – Medical Dictionary. Available online at http://www.medterms.com. Accessed 7 March 2011.
  10. Weinstein L. Syndrome of hemolysis elevated liver enzymes, and low platelet count: a severe consequence of hypertension in pregnancy. American Journal of Obstetrics and Gynecology. 1982. 142(2): 159-67.
  11. Dogan OO, Simsek Y, Celen S, Danisman N., Frequency of herediatary thrombophilia, anticoagulant activity, and homocysteine levels in patients with hemolysis, elevated liver functions and low thrombocyte count (HELLP) syndrome. Journal of Obstetrics and gynaecology research, March 6 2011 (epub ahead of print). Available at: http://www.ncbi.nlm.nih.gov/pubmed/21375667. Accessed 8 March 2011.
  12. Bacq Y. Liver diseases unique to pregnancy: A 2010 update. Clinics and Research in Hepatology and Gastroenterology. 2011; 20: (Article in Press) Available at http://www.ncbi.nlm.nih.gov/pubmed/21310683.
  13. Yamamoto H. Yamazaki K. Nishikawa S. Hayashi T. Hayakawa O. Kudo R., HELLP syndrome in a pregnant patient with a past history of splenectomy for idiopathic thrombocytopenic purpura. Case Report. Gynecology and Obstetrics. 1997. 259(2), 105-107.
  14. Schlembach D. Munz W. Fischer T., Effect of corticosteroids on HELLP syndrome: a case report. Journal of Perinatal Medicine, November 20, 2000. 28(6), 502-505.
  15. Kapan M. Evsen MS. Gumas M.. Onder A. Tekbas G., Subscapular Liver Hematoma in HELLP Syndrome: Case Report. Gastroenterology Research. June 2010. 3(3). 144-146.
  16. Basama FM. Granger K, Case Report: post partum class 1 HELLP syndrome. Gynecology and Obstetrics. 2007. 275(3) 187-189.