A retrospective analysis of the frequency of heparin-induced thrombocytopenia in the intensive care unit at a tertiary care center in Riyadh, Saudi Arabia.
Am J Blood Res 2023;13(6):198-206
www.AJBlood.us /ISSN:2160-1992/AJBR0152876
Original Article
A retrospective analysis
of the frequency of heparin-induced
thrombocytopenia in the intensive care
unit at a tertiary care center in Riyadh, Saudi Arabia
Ali H Mushtaq1,2, Abdulrahman W Rasheed2, Mouhamad G Jamil3, Khalid Maghrabi3, Osama Khoja3,
Muhammad R Sajid1, Hani Tamim1, Mohammad Hijazi3, Tarek Owaidah1,3
Al Faisal University, Riyadh, Saudi Arabia; 2Department of Internal Medicine, Cleveland Clinic Foundation,
Cleveland, Ohio, The United States of America; 3Department of Hematology, King Faisal Specialist Hospital and
Research Center, Riyadh, Saudi Arabia
1
Received August 11, 2023; Accepted December 21, 2023; Epub December 25, 2023; Published December 30,
2023
Abstract: Background: Heparin-induced thrombocytopenia (HIT) is an extremely serious and potentially fatal condition that can develop in patients taking heparin-based medications, such as unfractionated heparin (UFH) or lowmolecular-weight heparin (LMWH). The incidence and risk factors for HIT in critically ill patients, however, are not
well defined. Methods: We retrospectively collected data on HIT test results, route of heparin administration, age,
sex, heparin type (UFH or LMWH), and date of illness from patients admitted to the intensive care unit (ICU) and
regular nursing floor (non-ICU) at our hospital between January 2011 and December 2014. We screened patients
for HIT using the 4T score and confirmed the diagnosis through laboratory testing (direct enzyme immunoassay immunoglobulin G [IgG] or a platelet-activating antibody). Results: We screened a total of 946 patients, 56 (5.9%) of
whom were positive for HIT. Among 776 patients receiving UFH and 180 receiving LMWH, 2.8 and 6.6% developed
HIT, respectively (P = 0.051). We then classified our patients into two groups: ICU, and non-ICU. In the non-ICU
group (n = 317), 4 (2.7%) patients receiving LMWH and 25 (5.1%) receiving UFH were positive for HIT (P = 0.221).
In the ICU group (n = 639), 1 (3.1%) patient receiving LMWH and 26 (9.1%) receiving UFH were positive for HIT (P
= 0.249). The ICU group, therefore, had a higher cumulative incidence rate of HIT than the non-ICU group (8.5 vs.
4.5%). Conclusion: HIT was more common in ICU patients than non-ICU patients and in more patients receiving UFH
than LMWH, although the differences were not statistically significant. Early diagnosis and appropriate treatment
are essential to prevent adverse outcomes in patients with HIT.
Keywords: Heparin-induced thrombocytopenia, heparin, intensive care unit, critical illness, low molecular weight
heparin
Introduction
Heparin and its derivatives are widely used as
anticoagulants for the prevention and treatment of various medical conditions. Among the
most common applications of heparin are prophylaxis and treatment of deep venous thrombosis [1-4]. While hemorrhagic episodes are
the prevailing adverse effects associated with
heparin, some individuals are prone to developing thrombotic complications secondary to heparin-induced thrombocytopenia (HIT) [1]. HIT is
a severe and potentially fatal immunologically
mediated adverse drug reaction to heparin-
based medications, unfractionated heparin
(UFH), and low-molecular-weight heparin (LMWH). Medical professionals need to be more
aware of the presence of HIT to ensure its
detection, treatment, and prevention of its serious repercussions, especially considering relevant literature reports. HIT-related mortality is
estimated to be 20-30% [5]. The morbidity and
mortality of HIT are affected by the misdiagnosis of the condition, along with the misunderstanding of the course of the illness [1].
The incidence of HIT is significantly reduced in
patients receiving LMWH (0.1-0.5%) than in
https://doi.org/10.62347/GPME5540
Heparin-induced thrombocytopenia in intensive care unit
There is a paucity of studies analyzing the frequency of HIT in Saudi
Arabia, particularly in critically ill ICU
patients. The present study, therefore, aimed to retrospectively evaluate and compare the risk of developing HIT in association with the use of
UFH and LMWH, specifically in
patients admitted to medical wards
and ICUs. The present study was a
retrospective analysis of data from a
large tertiary care center in Riyadh,
Saudi Arabia.
Figure 1. Depicts the annual development of HIT from January 2011
to December 2014.
those receiving UFH (0.5-1%) [2, 4-8]. Numerous
patient and drug related factors influence the
likelihood of someone developing HIT, although
the factors most closely linked to an increased
likelihood of developing HIT include the length
of heparin therapy, type and dose of heparin
used, underlying indications for heparin treatment, and patient sex [8-10].
HIT should be suspected in patients who have
new complaints of new-onset thrombocytopenia, development of venous or arterial thromboses, or necrotic skin lesions at heparin injection
sites after receiving prolonged LMWH treatment or starting heparin within the preceding
5-10 days [11, 12]. Thrombocytopenia affects
95% of all patients with HIT and is caused by
platelet removal and consumption [13, 14]. HIT
is a highly prothrombotic state, and as a result,
25-64% of individuals with HIT develop arterial
or venous thromboses [2, 3, 5]. Thrombotic disorders can affect any part of the vasculature;
however, venous thrombosis is most commonly
observed and can cause gangrene, adrenal
hemorrhage, skin necrosis, and/or pulmonary
embolism [12, 15-17].
Diagnosing HIT can be challenging, especially
in critically ill patients in the intensive care unit
(ICU), where thrombocytopenia and thromboses are common for a variety of reasons [1822]. The overall incidence of HIT reported in ICU
patients is estimated to be between 0.4-3%
[23, 24]. In a German study of 12,528 medicalsurgical ICU patients, Selleng et al. [25] reported an incidence of HIT of 0.21%. Another large,
randomized trial of 3,764 patients found the
overall incidence of HIT to be 0.4% [6].
199
Materials and methods
We conducted a retrospective study
of all patients who received heparin
(UFH or LMWH) and were diagnosed with HIT
between January 2011 and December 2014 at
King Faisal Specialist Hospital and Research
Center (KFSHRC), Riyadh, Saudi Arabia (Figure
1). The data we collected included the HIT test
results, enzyme-linked immunosorbent assay
(ELISA) confirmation test results, age, sex, ICU
status, type of heparin (UFH or LMWH), and
route of administration (Table 1). We obtained
a total of 1190 patient records to include in our
study based on the following inclusive and
exclusive criteria.
Inclusive criteria: Patients admitted to our hospital between January 2011 and December
2014 who received preventative or therapeutic
doses of LMWH or UFH and underwent a HIT
test due to clinical suspicion. Thrombocytopenia
was defined as a >50% drop in platelet count
from baseline or ≥2 consecutive platelet counts
of <150,000 per mm3.
Exclusive (...truncated)