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ISSN: 1895-5770
Gastroenterology Review/Przegląd Gastroenterologiczny
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vol. 14
Original paper

Spontaneous splenic rupture related to anticoagulant and antiaggregant treatment

Ebubekir Gündeş
Ulaş Aday
Hüseyin Çiyiltepe
Durmuş Ali Çetin
Emre Bozdağ
Aziz Serkan Senger
Orhan Uzun
Selçuk Gülmez
Kamuran Cumhur Değer
Mustafa Duman

Gastroenterology Rev 2019; 14 (2): 152–156
Online publish date: 2019/07/05
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Trauma is the most frequent cause of splenic rupture. In contrast to traumatic rupture of the spleen, spontaneous splenic rupture (SSR) is a rare and life-threatening condition. There is only limited information about the characteristics of the patients, the incidence, and the aetiology of this condition. The most frequent causes of SSR include infectious diseases, medical procedures, and haematological diseases [1]. The most significant problems seen in this condition are delays in definitive diagnosis and the related destructive results in patients with no history of trauma.
Spontaneous splenic rupture related to anticoagulant and/or antiaggregant use is very rare, and literature on the subject only discusses it in the form of case reports [1, 2].


The objective of this study is to review the cases of patients with SSR who are receiving anticoagulant and/or antiaggregant treatment and who have no previous history of trauma; this study also seeks to identify the mode of treatment utilised for this very rare condition.

Material and methods

Study design

The cases of 6 patients with SSR between January 2013 and December 2016 at Gastroenterological Surgery Department, Kartal Koşuyolu High Speciality and Training Hospital were retrospectively evaluated. It was not necessary to obtain informed consent from the patients because of the retrospective nature of the study.

Study population

Patients who contracted SSR at the time of hospitalisation at the cardiology and cardiovascular surgery clinics, and who received conservative treatment or surgical procedures following our evaluation, were included in the study. Patients with a history of trauma and/or a history of laparotomy at the time of hospitalisation were excluded from the study.


Anamnesis, age, sex, accompanying diseases, and reasons for antiaggregant and/or anticoagulant prescriptions were recorded for all 6 patients following the review of their archive files and the hospital’s electronic archive system. The results of the following radiological diagnostic methods at the time of hospitalisation and diagnosis were also recorded: haematocrit (HCT), activated partial thromboplastin time (APTT), international normalised ratio (INR), and platelet (PLT) values.
Post-diagnostic medical and surgical modes of treatment for haematoma, the number of blood and blood product replacements, the rate of mortality, and the period of hospitalisation were investigated. Post-operative mortality cases during the first 30-day follow-up period were evaluated as operative mortality, while surgical complications that developed during this period were considered to be morbidity.
All the data were saved in Excel tables without any identifying information to protect the patients’ confidentiality and to prevent their names from being revealed.

Statistical analysis

Statistical Package for the Social Sciences (SPSS 21 Inc., Chicago, IL, USA) computer software was used for the bio-statistical analyses. When the data were presented as mean values their standard deviation values were also stated, and when the data were presented as median values their minimum–maximum values were also stated. Differences among the groups with normal distribution were compared using the t-test. The level of significance was set at the p < 0.05 level.


Baseline patient characteristics

Six patients with SSR were treated at our clinic during the time period of the study. Five (83.3%) of the 6 patients were male and 1 (16.6%) was female. Their mean age was 69.17 ±4.79 years. Each patient had at least one accompanying comorbidity. Three of the 6 patients had been receiving antiaggregant treatment only, while 2 had been receiving anticoagulant treatment only; just 1 of the 6 patients had been receiving both anticoagulant and antiaggregant treatments. The indications for anticoagulant and antiaggregant treatment of the patients were as follows: 2 patients received treatment for a coronary angiography-stent procedure, 1 patient received treatment following atrial fibrillation (AF), 1 patient received treatment following coronary arterial bypass graft (CABG), 1 patient received treatment following endovascular aneurysm repair (EVAR), and 1 patient received treatment for a peripheral arterial embolectomy procedure. The demographic features of the patients are presented in Table I.


The physical examination revealed that 5 of the patients had extensive abdominal sensitivity and distension. The abdominal examination of the patient that had not undergone surgery showed no distension, but there was sensitivity in the left quadrants. Three of the cases initially had undergone abdominal ultrasonography (USG), and all the patients, including those three, had undergone computerised tomography (CT) (Figures 1 A, B, 2 A, B). Patients with a mean HCT level of 35.17 ±2.3% at the time of hospitalisation also had a mean HCT level of 21.56 ±2.29% at the time of SSR diagnosis, and this decrease was statistically significant (p < 0.05). The median APTT level of the patients at the time of diagnosis was 42.75 s (28–89.6), their median INR level was 1.29 (1.1–2.19), and their median PLT value was 208 × 103/µl (105–244).


All the patients received red blood cell packs, and the mean amount of transfusion was 10.67 ±6.18 U. However, 1 of the patients had a history of CABG, while another had a history of EVAR. While 5 (83.33%) of the cases had splenectomy, 1 (16.66%) received conservative treatment. The preoperative status, diagnoses, and treatment modes of the patients are summarised in Table II. The mean duration of hospitalisation of the patients was 16.3 ±8.95 days, while the mean time of diagnosis for SSR was 6.33 ±5.08 days of hospitalisation.
Laparotomy had to be redone for 1 patient due to bleeding after surgery. Mortality was seen in 4 (66.6%) patients who underwent surgery. The patients’ follow-ups are summarised in Table III.


Atraumatic or SSR was first described by Orloff and Peskin in 1958, and four diagnostic criteria were established: the absence of history of trauma in the patient, the absence of perisplenic adhesions that could support previous traumas, the absence of diseases affecting the spleen, and a natural spleen, as determined using both microscopic and macroscopic analysis methods [3]. In all our patients, SSR developed during hospitalisation for other reasons, and they had no history of trauma.
A traumatic splenic rupture can appear as a complication of neoplastic, infectious, inflammatory, and genetic disorders. Various drugs and modes of treatment have also been associated with atraumatic splenic ruptures. A literature review by Aubrey-Bassler and Sowers in 2012 [4] reported on 47 cases with SSR related to drug use; of those cases, 22 of the patients were on anticoagulants, 13 were on thrombolytics, 10 were on recombinant granulocyte colony stimulating factor (G-CSF), and two were on anti-platelet agents. Both of the patients who were on anti-platelets were using ticlopidine. In their 2014 study of 12 cases with SSR, Kocael et al. [5] found anticoagulant use in three cases and acetyl salicylic acid (ASA) use in 1 case. In our study, 2 of the 3 patients who had been on anti-platelets were using clopidogrel, while one was using ASA.
The SSR shows a clinical progression similar to what is observed in patients with traumatic splenic rupture. Abdominal pain in the upper left quadrant, nausea, vomiting, dizziness, and syncope symptoms can be seen before shock symptoms [4, 5]. In general, our patients had abdominal pain. Abdominal examination also demonstrated that most of the patients had extensive sensitivity and distension symptoms.
Abdominal CT is the imaging method most frequently used for diagnosis [5]. However, some studies suggest that USG should be utilised [6]. Although 3 of the 6 patients in our study had undergone USG, all the patients had CT scans in order to exclude other intra-abdominal pathologies and to obtain a definitive diagnosis.
In their 845-case systematic review, Ranzulli et al. [7] stated that 84.1% of the cases had splenectomy, 1.2% had organ-protective surgery, and 14.7% were treated by conservative measures. Ranzulli et al. [7] also found the SSR-related mortality rate to be 12.2%. In our study, the mortality rate was found to be much higher than in that study. We believe that this difference is due to several factors. First, our patients contracted SSR at the time of hospitalisation for cardiac reasons. Second, our SSR patients had accompanying diseases.
Third, our patients were elderly. Fourth, the use of anticoagulant and antiaggregant treatments increased the amount and severity of bleeding.


Consequently, SSR is a condition that should be taken into consideration in differential diagnosis because it could lead to serious mortality in cases with newly developed abdominal pain and low HCT levels in patients who are hospitalised for cardiac reasons and are taking anticoagulant and/or antiaggregant medication.

Conflict of interest

The authors declare no conflict of interest.


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