<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0138-600X</journal-id>
<journal-title><![CDATA[Revista Cubana de Obstetricia y Ginecología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Cubana Obstet Ginecol]]></abbrev-journal-title>
<issn>0138-600X</issn>
<publisher>
<publisher-name><![CDATA[Editorial Ciencias Médicas]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0138-600X2016000400011</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[The Woman with Severe Preeclampsia Who Died from Postpartum Complications]]></article-title>
<article-title xml:lang="es"><![CDATA[Paciente con preeclampsia severa muere por complicaciones posparto]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gashi]]></surname>
<given-names><![CDATA[Astrit M]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,University Clinical Centre of Kosovo Department of Obstetrics and Gynecology ]]></institution>
<addr-line><![CDATA[ Pristine]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>12</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>12</month>
<year>2016</year>
</pub-date>
<volume>42</volume>
<numero>4</numero>
<fpage>519</fpage>
<lpage>523</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_arttext&amp;pid=S0138-600X2016000400011&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_abstract&amp;pid=S0138-600X2016000400011&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.sld.cu/scielo.php?script=sci_pdf&amp;pid=S0138-600X2016000400011&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Preeclampsia is clinically defined by hypertension and proteinuria, with or without pathologic edema that occurs after 20 weeks' gestation, but can also present up to 4-6 weeks post-partum. Worldwide, incidence of preeclampsia is 5-14 percent of all pregnancies, while severe preeclampsia can develop to about 25 percent of all cases of preeclampsia. Severe preeclampsia is a pathology characterized by endothelial dysfunction that can often be complicated, and thus may lead to liver and renal failure, disseminated intravascular coagulopathy (DIC), and central nervous system (CNS) abnormalities. Worldwide, preeclampsia and eclampsia is responsible for about 14 percent of maternal deaths per year. We present a case, from our clinic, which has had serious complications after birth and that ended with the death of the patient. Despite the adequate management with the timely diagnosis and therapy, patient died ten days after Caesarean delivery.]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[La preeclampsia se define clínicamente por la presencia de hypertension y proteinuria, con o sin edema patológico, y aparece luego de las 20 semanas de gestación, pero también puede presentarse de 4 a 6 semanas después del parto. En el ámbito internacional, la incidencia de la preeclampsia oscila entre 5 y 14 % de todos los embarazos mientras que la preeclampsia severa puede desarrollarse en el 25 % aproximadamente de todos los casos de preeclampsia. La preeclampsia severa es una patología que se caracteriza por la disfunción endothelial con complicaciones frecuentes y de ahi puede originarse la insuficiencia renal y hepatica, la coagulopatía intravascular diseminada y las anomalías en el sistema nervioso central. Ambos trastornos son responsables aproximadamente del 14 % de las muertes maternas en el mundo. Se presenta el caso de una paciente de nuestra clínica que sufrió graves complicaciones tras el parto y murió a consecuencia de ello. A pesar del cuidado adecuado, el diagnóstico y el tratamiento oportunos, esta paciente falleció diez dias después del parto por cesárea.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[severe preeclampsia]]></kwd>
<kwd lng="en"><![CDATA[postpartum]]></kwd>
<kwd lng="en"><![CDATA[complications]]></kwd>
<kwd lng="es"><![CDATA[preeclampsia severa]]></kwd>
<kwd lng="es"><![CDATA[posparto]]></kwd>
<kwd lng="es"><![CDATA[complicaciones]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  <font face="Verdana, Arial, Helvetica, sans-serif" size="2"></font>    <p align="right"> <font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>PRESENTACI&#211;N    DE CASO</b> </font></p>     <p>&nbsp; </p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b><font size="4">The    Woman with Severe Preeclampsia Who Died from Postpartum Complications</font></b>    </font></p>     <p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b><font size="3">Paciente    con preeclampsia severa muere por complicaciones posparto</font></b> </font></p>     <p>&nbsp;</p>     <p>&nbsp; </p>     <p> <font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Astrit M. Gashi    </b> </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Department of Obstetrics    and Gynecology, University Clinical Centre of Kosovo, Pristine.</font></p>     ]]></body>
<body><![CDATA[<p>&nbsp;</p>     <p>&nbsp;</p> <hr size="1" noshade>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>ABSTRACT </b>    </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> Preeclampsia is    clinically defined by hypertension and proteinuria, with or without pathologic    edema that occurs after 20 weeks' gestation, but can also present up to 4-6    weeks post-partum. Worldwide, incidence of preeclampsia is 5-14 percent of all    pregnancies, while severe preeclampsia can develop to about 25 percent of all    cases of preeclampsia. Severe preeclampsia is a pathology characterized by endothelial    dysfunction that can often be complicated, and thus may lead to liver and renal    failure, disseminated intravascular coagulopathy (DIC), and central nervous    system (CNS) abnormalities. Worldwide, preeclampsia and eclampsia is responsible    for about 14 percent of maternal deaths per year. We present a case, from our    clinic, which has had serious complications after birth and that ended with    the death of the patient. Despite the adequate management with the timely diagnosis    and therapy, patient died ten days after Caesarean delivery. </font></p>     <p> <font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Key words:</b>    severe preeclampsia; postpartum; complications </font></p> <hr size="1" noshade>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>ABSTRACT</b>    </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">La preeclampsia    se define cl&#237;nicamente por la presencia de hypertension y proteinuria,    con o sin edema patol&#243;gico, y aparece luego de las 20 semanas de gestaci&#243;n,    pero tambi&#233;n puede presentarse de 4 a 6 semanas despu&#233;s del parto.    En el &#225;mbito internacional, la incidencia de la preeclampsia oscila entre    5 y 14  % de todos los embarazos mientras que la preeclampsia severa puede desarrollarse    en el 25 % aproximadamente de todos los casos de preeclampsia. La preeclampsia    severa es una patolog&#237;a que se caracteriza por la disfunci&#243;n endothelial    con complicaciones frecuentes y de ahi puede originarse la insuficiencia renal    y hepatica, la coagulopat&#237;a intravascular diseminada y las anomal&#237;as    en el sistema nervioso central. Ambos trastornos son responsables aproximadamente    del 14 % de las muertes maternas en el mundo. Se presenta el caso de una paciente    de nuestra cl&#237;nica que sufri&#243; graves complicaciones tras el parto    y muri&#243; a consecuencia de ello. A pesar del cuidado adecuado, el diagn&#243;stico    y el tratamiento oportunos, esta paciente falleci&#243; diez dias despu&#233;s    del parto por ces&#225;rea. </font></p>     <p> <font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Palabras claves:    </b> preeclampsia severa; posparto; complicaciones. </font></p> <hr size="1" noshade>     <p>&nbsp;</p>     <p>&nbsp; </p>     ]]></body>
<body><![CDATA[<p> <font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b><font size="3">INTRODUCTION    </font> </b> </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> Pre-eclampsia    is clinically defined by hypertension and proteinuria, with or without pathological    oedema that occurs after 20 weeks' gestation, but can also present up to 4-6    weeks post-partum.<sup>1</sup> </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> Severe features    of Preeclampsia include any of the following features; </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> (a) Systolic blood    pressure of 160 mm Hg or higher, or a diastolic blood pressure of 110 mm Hg    or higher on two occasions at least 4 hours apart while the patientis on bed    rest (unless antihypertensive therapy is initiated before this time). </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> (b) Thrombocytopenia    (platelet count less than 100.000/microliter). </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> (c) Impaired liver    function as indicated by abnormally elevated blood concentration of liver enzymes    (to twice normal concentration), severe persistent right upper quadrant or [epigastric    pain unresponsive to medication and not accounted by alternative diagnosis,    or both. </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> (d) Progressive    renal insufficiency (serum creatinine concentration greater than 1.1 mg/dl or    a doubling of the serum creatinine concentration in the absence of other renal    disease). </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> (e) Pulmonary    edema. </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> (f) New-onset    cerebral or visual disturbances. </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> Worldwide, incidence    of pre-eclampsia is 5-14 percent of all pregnancies. In developing nations,    incidence of pre-eclampsia is 4-18 percent.<sup>2,3</sup> Severe pre-eclampsia    can develop to approximately 25 percent of all cases of pre-eclampsia.<sup>4</sup>    Morbidity and mortality in pre-eclampsia and eclampsia are frequent. Severe    pre-eclampsia may lead to liver and renal failure, disseminated intravascular    coagulopathy (DIC), and central nervous system (CNS) abnormalities. In world,    preeclampsia and eclampsia is responsible for approximately 14 percent of maternal    deaths per year (50,000-75,000). <sup>5</sup> A woman with severe preeclampsia,    and complicated with eclampsia or HELLP syndrome, has a 20 % risk of developing    preeclampsia in her subsequent pregnancy.<sup>6-11</sup> </font></p>     ]]></body>
<body><![CDATA[<p>&nbsp;</p>     <p> <font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b><font size="3">CASE    PRESENTATION </font> </b> </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> A 34-year-old    woman pregnant presented in Department of Obstetrics and Gynecology, University    Clinical Centre of Kosovo, with 29 weeks'gestation and dyspnoea, expressed cyanosis,    tachycardia, and epigastric pain. At the admission office, she had a blood pressure    of 160/95 mmHg; pulse of 105 beats per minute, oxygen saturation was 96. On    physical examination, congenital deformity of the spine (kyphoscoliosis) was    noticed. Skin and mucous membranes were pale. Data from the history show that    the patient was treated by easy preeclampsia, from week 25 of gestation. Laboratory    findings; hemograme was normal, urine analysis (protein 1+). Biochemical laboratory    tests: serum aspartate aminotransaminase (AST), 67 IU/L; serum alanine aminotransaminase    (ALT), 120 IU/L; serum lactate dehydrogenase (LDH), 839 IU/L; serum urea 10.74    mmol/L and creatinine was normal; Triglyceride, 3.49mmol/L; hemoglobin and platelet    count were normal. Coagulation profile was normal. After consultations with    a cardiologist, anesthesiologist and pulmonologist, patient was found to be    having acute pulmonary edema. Ultrasound and Echocardiography revealed pericardial    effusion, and other parameters anatomical structure of the heart were found    normal. Chest x-ray, electrocardiogram and all necessary imaging examinations    were also performed. Patient was transferred to intensive care unit, where she    was intubated and connected to the respiratory apparatus. The ultimate diagnosis:    29 weeks pregnant, Preeclampsia, Pericardial effusion, pulmonary edema, Respiratory    insufficiency, Kyphoscoliosis, Neurofibromatosis, Rh incompatibility (Patient    a week earlier, at week 28 of gestation was treated with 300 mcg of Rh IgG (RhoGAM),    intramuscular injection). After stabilization of vital parameters for several    hours, it was decided to terminate the pregnancy after a written consent of    the patient. A Pfannenstiel incision was made and a female fetus was delivered    weighing 1340 grams with Apgar score of 1 in the first minute and 3 in the fifth    minute. The patient was treated with supplementary oxygen, crystalloid, antibiotics,    H2- blockers, LMWH, B-blockers, diuretic, analgesic, vitamin preparations, mucolytics,    corticosteroids,anti-hypertensive and antiemetic. After a week of treatment    in intensive care unit, the patient's condition improved, and therefore was    extubated and shifted back to the Department of Obstetrics and Gynaecology under    monitoring of cardiologist, anaesthesiologist and pulmonologist. After seven    days, patient's condition rapidly deteriorated and went into cardiac arrest.    Despite the resuscitation measures taken, it unfortunately ended up in her death    after 10 days of cesarean delivery postpartum (exitus letalis). </font></p>     <p>&nbsp;</p>     <p> <font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b><font size="3">DISCUSSION</font></b>    </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> Preeclampsia is    the disease of widespread vascular endothelial malfunction and generalized vasospasm.    However, the pathophysiologic mechanism for preeclampsia is very complex. Severe    preeclampsia can develop to approximately 25 percent of all cases of preeclampsia    [4]. Worldwide, preeclampsia and eclampsia is responsible for approximately    14 percent of maternal deaths per year [5]. This disease may lead to liver and    renal failure, disseminated intravascular coagulopathy (DIC), and central nervous    system (CNS) abnormalities. Preeclampsia/eclampsia is one of the leading causes    of maternal morbidity and mortality worldwide. Failure of clinicians to predict    the impending life-threatening complications from preeclampsia may contribute    to rise in maternal mortality due to this disease and its associated complications.    </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> Early detection/diagnosis    and appropriate management is extremely important in patients with preeclampsia,    for better maternal as well as perinatal outcome. </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> Clinician must    perform a detailed assessment along with thorough history taking (including    the symptoms of severe preelampsia and physical examination. Laboratory tests    such as a complete blood count with platelet count, and assessment of serum    creatinine and liver enzymes levels, evaluation for urine protein (24-hour collection    or protein/creatinine ratio) may aid to establish the diagnosis. Fetal evaluation    should be performed including antepartum fetal surveillance. </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> Preeclampsia is    a pregnancy-specific hypertensive disorder with multisystem involvement. Severe    preeclampsia can result in both acute and long term complications for both the    woman and her newborn. Maternal complications of severe preeclampsia include    pulmonary edema, myocardial infarction, stroke, acute respiratory distress syndrome,    coagulopathy, severe renal failure and retinal injury. These complications are    more likely to occur in the presence of pre-existent medical disorders and with    acute maternal organ dysfunction related to preeclampsia. Fetal and newborn    complications of severe preeclampsia result from exposure to uteroplacental    insufficiency or from preterm birth, or both. According to ACOG (2013), for    women with severe preeclampsia at or beyond 34 0/7 weeks of gestation, and in    those with unstable maternal-fetal conditions irrespective of gestational age,    delivery soon after maternal stabilization is recommended. </font></p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p> <font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b><font size="3">CONCLUSION</font></b>    </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> This case report    of patient who presented with 29 weeks of pregnancy with: dyspnoea, expressed    cyanosis, tachycardia and epigastric pain to our clinical center. She developed    complications associated with severe preeclampsia and unfortunately ended up    with fatal outcome after 10 days of cesarean delivery post-partum, despite of    timely diagnosis and adequate management. </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> Preeclampsia/ecclampsia    is associated with substantial maternal complications, both acute and long-term.    Clear protocols for early detection and management of hypertension in pregnancy    at all levels of health care are required for better maternal as well as perinatal    outcome. </font></p>     <p>&nbsp;</p>     <p> <font face="Verdana, Arial, Helvetica, sans-serif" size="2"><b>Conflict of    Interests</b> </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> All the authors    not have any conflict of interests. </font></p>     <p>&nbsp;</p>     <p> <font face="Verdana, Arial, Helvetica, sans-serif"><b>BIBLIOGRAPHIC REFERENCES</b></font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 1. Lagana AS,    Favilli A, Triolo O, Granese R, Gerli S. Early serum markers of pre-eclampsia:    are we stepping forward? J Matern Fetal Neonatal Med. 2015:1-5.     </font></p>     ]]></body>
<body><![CDATA[<!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 2. Villar J, Betran    AP, Gulmezoglu M. Epidemiological basis for the planning of maternal health    services. WHO/RHR. 2001.     </font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 3. Khedun SM,    Moodley J, Naicker T. Drug management of hypertensive disorders of pregnancy.    PharmacolTher. 1997;74(2):221-58.     </font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 4. Sibai BM. Magnesium    sulfate prophylaxis in preeclampsia: Lessons learned from recent trials. Am    J Obstet Gynecol. 2004;190(6):1520-6.     </font></p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 5. WHO, 2004.    Bethesda, MD. Global Burden of Disease for the Year 2001 by World Bank    Region, for Use in Disease Control Priorities in Developing Countries, National    Institutes of Health: WHO. Make every mother and child count. 2nd ed.   World Health Report, 2005, Geneva:World Health Orga. </font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 6. Sibai BM, Ramadan    MK, Chari RS. Pregnancies complicated by HELLP syndrome (hemolysis, elevated    liver enzymes, and low platelets): subsequent pregnancy outcome and long-term    prognosis. Am J Obstet Gynecol. 1995;172(1 Pt 1):125-9.     </font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 7. Chames MC,    Haddad B, Barton JR. Subsequent pregnancy outcome in women with a history of    HELLP syndrome at &lt; or = 28 weeks of gestation. Am J Obstet Gynecol.    2003;188(6):1504-7; discussion 1507-8.     </font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 8. Sibai BM, Sarinoglu    C, Mercer BM. Eclampsia. VII. Pregnancy outcome after eclampsia and long-term    prognosis. Am J Obstet Gynecol. 1992;166(6 Pt 1):1757-61; discussion    1761-3.     </font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 9. Lopez-Llera    M, Hernandez Horta JL. Pregnancy after eclampsia. Am J Obstet Gynecol.    1974;119(2):193-8.     </font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 10. Adelusi B,    Ojengbede OA. Reproductive performance after eclampsia. Int J Gynaecol Obstet.    1986;24(3):183-9.     </font></p>     <!-- ref --><p><font face="Verdana, Arial, Helvetica, sans-serif" size="2"> 11. Sibai BM,    Mercer B, Sarinoglu C. Severe preeclampsia in the second trimester: recurrence    risk and long-term prognosis. Am J Obstet Gynecol. 1991;165(5 Pt 1):1408-12.        </font></p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p>&nbsp;</p>     <p><font face="Verdana, Arial, Helvetica, sans-serif" size="2">Recibido: 17 de    julio de 2016.    <br>   Aprobado: 7 de octubre de 2016.</font></p>     <p>&nbsp;</p>     <p>&nbsp; </p>      ]]></body><back>
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