|Year : 2019 | Volume
| Issue : 1 | Page : 40-42
Mallory-Weiss Syndrome complicating pregnancy – A rare near miss
Isha Chopra1, Sunil T Pandya1, Mangalampally Kiran Kumar1, Surapaneni Tarakeswari2, Hemamalini2, Madapu Manokanth1, Prabhakar Boddu3
1 Department of Anaesthesia, Pain Medicine and Obstetric Critical Care, Fernandez Hospital, Hyderabad, Telangana, India
2 Department of Obstetric Medicine, Fernandez Hospital, Hyderabad, Telangana, India
3 Department of Medical Gastroenterology, Century Hospital, Hyderabad, Telangana, India
|Date of Web Publication||11-Apr-2019|
Dr. Isha Chopra
Department of Anaesthesia, Pain Medicine and Obstetric Critical Care, Fernandez Hospital, Hyderabad, Telangana
Source of Support: None, Conflict of Interest: None
Mallory-Weiss syndrome (MWS) rarely occurs during pregnancy and can lead to massive bleed if occurring in the third trimester. Unrecognized MWS may lead to life threatening hemorrhage and shock affecting maternal and fetal well-being. We describe a rare case of MWS in a pregnant patient at 36 weeks of gestation with underlying pre-eclampsia, acute kidney injury, and hemodynamic instability. The possibility of mucosal tears should be kept in mind in the absence of an obvious source of bleeding.
Keywords: Mallory-Weiss syndrome, pre-eclampsia, pregnancy, severe anemia
|How to cite this article:|
Chopra I, Pandya ST, Kumar MK, Tarakeswari S, Hemamalini, Manokanth M, Boddu P. Mallory-Weiss Syndrome complicating pregnancy – A rare near miss. J Obstet Anaesth Crit Care 2019;9:40-2
|How to cite this URL:|
Chopra I, Pandya ST, Kumar MK, Tarakeswari S, Hemamalini, Manokanth M, Boddu P. Mallory-Weiss Syndrome complicating pregnancy – A rare near miss. J Obstet Anaesth Crit Care [serial online] 2019 [cited 2021 Jan 15];9:40-2. Available from: https://www.joacc.com/text.asp?2019/9/1/40/255894
| Introduction|| |
Mallory-Weiss syndrome More Details (MWS) refers to an upper gastrointestinal (GI) bleeding disorder that occurs secondary to a sharp rise in intra-esophageal or intra-gastric pressure. Common inciting factors include episodes of severe vomiting, retching, or hiccups as in patients with alcoholism, bulimia, hiatus hernia, infectious gastritis or those receiving gastroscopy. The syndrome has been less commonly attributed to hyperemesis gravidarum in first trimester of pregnancy, and on rare occasions, it has occurred during third trimester or even postnatally.
We report a case of Mallory-Weiss tear More Detailss diagnosed at 36 weeks gestation that manifested with dark tarry stools, hemorrhagic shock, and multi-organ failure.
| Case Report|| |
A 35-year-old woman, unbooked primipara with 36 weeks gestation presented to our emergency department with severe pre-eclampsia, complaint of severe dizziness and difficulty breathing for 10 days. She gave a history of loss of appetite and dark tarry stools for the same period. She also complained of excessive vomiting and retching during this period. Her antenatal history included pre-eclampsia (tablet labetalol 100 mg TID) started 2 months earlier as BP readings were 180/110 mmHg, gestational diabetes (human actrapid insulin), and hypothyroidism (tablet thyroxine 100 mg) all of which were well controlled with moderate doses of medications. There were no clinical and laboratory features of severe pre-eclampsia. She was found positive for sickle cell trait 2 months back and was put on aspirin 150 mg once daily for pre-eclampsia. During her antenatal visits, she was found to have iron deficiency anemia and was prescribed hematinics. Her last hemoglobin before this admission was 9.2 gm/dl.
At the time of this admission, her blood pressure was 100/70 mmHg, pulse rate was 140 beats/min, and oxygen saturation was 95%. Laboratory examinations revealed a sudden drop in hemoglobin from 9.2 to 3.9 gm/dl. Serum creatinine was found to be 2.9 mg/dl with a blood urea of 80 mg/dl. Coagulation profile was normal. Two units of packed red blood cells were transfused, and an infusion of proton pump inhibitor was started. Parenteral iron supplements were also started. After initial stabilization, an upper GI endoscopy was done, which showed Mallory-Weiss tears in the healing phase [Figure 1]. The patient was kept under observation for few days to rule out any further episodes of bleeding. Her melena improved, creatinine decreased from 2.9 to 2.0, and hemoglobin rose to 6.2 gm/dl. Tests done to rule out connective tissue disorders were borderline positive for ds DNA, ssB, and antinucleosomes. Emergency section was performed under neuraxial block for non-reactive non-stress test (NST) and presumed fetal compromise after 3 days. She had an uneventful surgery with minimal blood loss of 300 ml intraoperatively. She was transfused two more units of packed red blood cells in the postoperative period to correct her pre-existing anemia. Her hemoglobin increased to 8 gm/dl and her serum creatinine came as 1.9. She was discharged home after 3 days.
|Figure 1: Upper gastrointestinal endoscopy with linear tears at gastro-esophageal junction|
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| Discussion|| |
MWS is the clinical sequelae of longitudinal tears of the esophageal wall usually at the gastro-esophageal junction, which may affect only the esophageal mucosa or penetrate through the entire esophageal wall. MWS reflects 3%–15% of all the cases of upper GI hemorrhage. The exact incidence of this syndrome in pregnancy is not known.
It was first described in 1929 by George Kenneth Mallory, an American pathologist and Soma Weiss, an American physician in patients with persistent retching and alcoholic binge. Clinically, MWS may occur in any individual with severe bouts of retching, coughing or vomiting or after any event that provokes a sudden rise in the intra-gastric pressure. Commonly, the patients present with dyspepsia, abdominal pain, hematemesis, melena, back pain, and in some instances, with features of hemorrhagic shock. Hematemesis is the most common presenting feature, whereas melena, hematochezia, syncope, and abdominal pain are less common. Knauer CM has reported a significant number of instances where salicylate ingestion is linked to Mallory-Weiss tears, attributing to approximately, 30% cases of MWS. In most of the patients, the bleeding subsides with conservative management but 5%–35% patients may need endoscopic therapy such as hemoclipping, thermocoagulation, balloon tamponade, or diluted epinephrine injection. The presence of shock at initial presentation and active bleeding are independent risk factors for predicting recurrent bleeding in patients with this syndrome.
MWS is infrequent during pregnancy. Most cases reported in literature have occurred during the first trimester, usually owing to hyperemesis gravidarum. Very few cases have been reported to occur during the third trimester, and most of those patients had underlying pathology such as scleroderma or acute fatty liver.,
If there are no contraindications, a central neuraxial block is the ideal anesthetic technique in these patients and it confers good hemodynamics stability. Epidural analgesia should be offered to laboring women, and active bearing down efforts should be avoided. Second stage of labor should be cut short with assisted vaginal delivery. For all patients who require general anesthesia for cesarean or non-obstetric surgery, they should be considered full stomach and must be given adequate acid aspiration prophylaxis. Induction and extubation should be conducted as per the standard protocol. Rapid sequence induction should be the rule. Further, it is of paramount importance to suppress the laryngo sympathetic response during intubation and extubation. Several studies have advocated the use of dexmedetomidine, an alpha-2 agonist, to achieve hemodynamic stability and suppress the pressor response seen at intubation and extubation. We should always be prepared for urgent perioperative blood transfusions and emergency endoscopic hemostasis in these patients if the need arises. Acid aspiration prophylaxis should be continued in the postoperative period also.
We postulate that in our case, the cause of Mallory-Weiss tears was pregnancy induced retching and vomiting secondary to pre-eclampsia, compounded by aspirin 150 mg once a day that was started in view of pre-eclampsia. This led to melena, severe anemia, and hypotension with hemodynamic instability and acute kidney injury. Further, as systemic lupus erythematosus (SLE) profile was borderline positive, she would again need a repeat screening after 12 weeks. Whether she had acute on chronic kidney insufficiency also needs follow-up, though radiologically, there were no features of chronic kidney disease.
Upper GI endoscopy has a diagnostic accuracy of greater than 90%. Bleeding from the tears usually stops spontaneously and healing occurs with conservative treatment in most patients. Hence, endoscopy should be done whenever there is unexplained drop in hemoglobin, especially, when stool for occult blood is positive or has history suggesting gastro-intenstinal (GI) bleeding to minimize near misses that sometimes can prove fatal.
| Conclusion|| |
We present a very rare case report of MWS in pregnancy, a rare near miss. One should suspect and have a low threshold for upper GI endoscopy, when a pregnant patient presents with severe vomiting with clinically apparent GI bleed, melena, or unexplained acute anemia.
All authors contributed to the concept and intellectual content, literature review, data acquisition and analysis, and manuscript preparation, review, and editing.
The manuscript has been read by all authors and each author believes the manuscript represents honest work.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
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