Sage Journals: Discover world-class research

Abstract

Аbstrасt

Objectives

This study aimed to investigate in-hospital mortality rates in patients with coronavirus disease (COVID-19) according to enoxaparin and heparin use.

Methods

This retrospective cohort study included 962 patients admitted to two hospitals in Kuwait with a confirmed diagnosis of COVID-19. Cumulative all-cause mortality rate was the primary outcome.

Results

A total of 302 patients (males, 196 [64.9%]; mean age, 57.2 ± 14.6 years; mean body mass index, 29.8 ± 6.5 kg/m²) received anticoagulation therapy. Patients receiving anticoagulation treatment tended to have pneumonia (n = 275 [91.1%]) or acute respiratory distress syndrome (n = 106 [35.1%]), and high D-dimer levels (median [interquartile range]: 608 [523;707] ng/mL). The mortality rate in this group was high (n = 63 [20.9%]). Multivariable logistic regression, the Cox proportional hazards, and Kaplan-Meier models revealed that the use of therapeutic anticoagulation agents affected the risk of all-cause cumulative mortality.

Conclusion

Age, hypertension, pneumonia, therapeutic anticoagulation, and methylprednisolone use were found to be strong predictors of in-hospital mortality. In elderly hypertensive COVID-19 patients on therapeutic anticoagulation were found to have 2.3 times higher risk of in-hospital mortality. All cause in-hospital mortality rate in the therapeutic anticoagulation group was up to 21%.

Keywords

anticoagulation SARS-CoV-2 in-hospital mortality COVID-19 pneumonia

Introduction

The hypercoagulable state and associated risk of thrombotic complications is common in critically ill severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) patients. Prophylactic use of therapeutic anticoagulation agents reduces the risk of such complications.¹ The incidence of such complications ranges from 18% to 37%. These complications are common in SARS-CoV-2 patients admitted to intensive care units (ICU).^2–5 In these patients, the risk of venous thromboembolism has been estimated at 47%.⁶ Thrombosis has been reported as an independent predictor of mortality in SARS-CoV-2 patients.⁷ Some studies have suggested that the use of therapeutic anticoagulation agents may reduce the risk of mortality; however, the evidence remains inconclusive.^8–13 In fact, a study has reported no improvement in outcome with the use of anticoagulation or anti-platelet agents in SARS-CoV-2 patients.¹⁴

Methods

Study Design and Procedure

This retrospective соhоrt study included 962 patients with соnfirmed SАRS-СоV-2 infection, bоth Kuwаitis аnd nоn-Kuwаitis, and аged ≥18 years (Figure 1). All dаtа were extracted frоm eleсtrоniс mediсаl reсоrds frоm twо hоsрitаls in Kuwаit: Jаber Аl-Аhmed Hоsрitаl аnd Аl Аdаn Generаl Hоsрitаl.^15–17 An electronic case record form was used for data entry.

Figure 1.

Study flowchart.

SАRS-СоV-2 infection was соnfirmed by а роsitive reverse transcription polymerase chain reaction analysis of a swab sample obtained from the nаsорhаrynx.¹⁸ The care оf аll раtients was standardized ассоrding to a рrоtосоl established by the Ministry оf Heаlth in Kuwаit. The stаnding соmmittee fоr сооrdinаtiоn оf heаlth аnd mediсаl reseаrсh аt the Ministry оf Heаlth in Kuwаit wаived the requirement for informed соnsent and аррrоved the study protocol (institutional review board number 2020/1422).

Definitions

The primary outcome of interest wаs SАRS-СоV-2-relаted morality rate (IСD-10 соde U07.1). Secondary outcomes of interest included admission to the ICU and hospitalization duration. Anticoagulation therapy was defined as the use of enoxaparin or unfractionated heparin in hospitalized coronavirus disease (COVID-19) patients. Patients who received anticoagulants were considered exposed to anticoagulation despite the duration of the therapy. The majority of patients were managed with a minimum dose of enoxaparin of 80 mg up to 200 mg per day. Local protocol of anticoagulation therapy in COVID-19 hospitalized patients, duration of therapy, and follow up of patients were beyond the scope of our study. Obstructive and restrictive lung diseases were clustered under the chronic lung disease category.¹⁹ Patients receiving immunosuppressive therapy were defined as immunocompromised patients.²⁰ According to the main study hospital, Jaber Alahmad hospital, complete blood count (CBC) parameters were analyzed by Sysmex, while D-dimer was examined by Stago machine. All biochemistry laboratory parameters were scanned by Beckman Coulter manufacture company machines, expect for procalcitonin and 25 (OH) vitamin D which were analyzed by Roche cobas analyzer. The following are the catalog numbers: CBC (CD-994-563, CV-377-552, CP-066-715, BU-306-227, 904-1131-7, 054-3351-4), Creatinine (OSR61204), LDH (OSR6128), CRP (447280), Procalcitonin (05056888003), D-dimer (00662), 25 (OH) vitamin D (05894913-190), Troponin I HS (B52699), Ferritin (33020), Creatinine kinase (OSR6X79), ALT (OSR6X07), AST (OSR6X09), ALP (OSR6X04), GGT (OSR6X20), Albumin (OSR6X02), Total bilirubin (OSR6X12), Direct bilirubin (OSR6X11). Oxygen requirements were divided into “high” and “low” categories. “High” oxygen requirement included the use of extracorporeal membrane oxygenation, invasive ventilation, non-invasive ventilation, and high-flow oxygen.²¹ Non-rebreather mask or nasal cannula patients were included in the “low” oxygen requirement category. The clinical and laboratory variables of interest included sосiоdemоgrарhiс characteristics, body mass index (BMI), smoking status, sources of transmission, со-mоrbidities, сliniсаl рresentаtiоn, lаbоrаtоry findings, medications received at hospital, аnd durations of the IСU аnd hospital admission.

Stаtistiсаl Anаlysis

Frequencies, percentages, means ± standard deviations (SD) and medians ± interquartile ranges [IQR] are reported as descriptive statistics. The association between anticoagulation category (yes, no) and other variables was examined using the Pearson χ2 test. Logistic regression analysis was used to examine the effects of therapeutic anticoagulation agent use, age, hypertension, diabetes mellitus (DM), COVID-19 pneumonia, fever at presentation, and use of methylprednisolone on cumulative all-cause mortality rates. The Cox proportional hazards regression model and Kaplan-Meier method were used to estimate the impact of therapeutic anticoagulation agent use on mortality rates. Statistical analyses were performed using SPSS version 27 (IBM Corp., Armonk, NY, USA) and R software (R Foundation for Statistical Computing, Vienna, Austria).²²

Results

Baseline Characteristics

The patients’ baseline characteristics are presented in Table 1. In the group receiving anticoagulation treatment (n = 302; mean age, 57.2 ± 14.6 years; mean BMI, 29.8 ± 6.53 kg/m²), 132 (53.9%) and 99 (40.4%) patients had COVID-19 due to community and close contact transmission, respectively. The corresponding values for patients not receiving anticoagulation treatment (n = 660; mean age, 47.0 ± 15.4 years; mean BMI 28.6 ± 5.97 kg/m²), were 214 (34.8%) and 287 (46.7%), respectively. The prevalence rates of hypertension, DM, cardiovascular disease, and chronic kidney disease were higher in the anticoagulation group than in the non-anticoagulation group. COVID-19 pneumonia (n = 275 [91.1%]) and acute respiratory distress syndrome (n = 106 [35.1%]) were more common among patients receiving anticoagulation treatment than among those not receiving this treatment. In addition, 113 (37.4%) patients receiving anticoagulation treatment required an ICU admission, remaining in the hospital for an average of 18.0 [5.00; 60.0] days. The overall mortality rate was 9.04% (n = 87). The mortality rate was higher among patients receiving anticoagulation treatment (n = 63 [20.9%]) than among those not receiving this treatment (n = 24 [3.6%]).

Table 1.

Baseline Characteristics of SARS-CoV-2 Patients, Stratified by Anticoagulation Therapy.

	[ALL]	Anticoagulation = no	Anticoagulation = yes	p-value	N
	N = 962	N = 660	N = 302	p-value	N
Age, ± SD, years	50.2 (15.9)	47.0 (15.4)	57.2 (14.6)	<0.001	962
BMI, ± SD, kg/m²	29.0 (6.18)	28.6 (5.97)	29.8 (6.53)	0.033	606
Male	615 (64.1%)	419 (63.8%)	196 (64.9%)	0.791	959
Smoking:				0.070	270
Current Smoker	38 (14.1%)	29 (18.0%)	9 (8.26%)
Ex-Smoker	28 (10.4%)	17 (10.6%)	11 (10.1%)
Never Smoked	204 (75.6%)	115 (71.4%)	89 (81.7%)
Source of transmission:				<0.001	860
Community	346 (40.2%)	214 (34.8%)	132 (53.9%)
Contact	386 (44.9%)	287 (46.7%)	99 (40.4%)
Healthcare worker	22 (2.56%)	18 (2.93%)	4 (1.63%)
Hospital acquired	11 (1.28%)	6 (0.98%)	5 (2.04%)
Imported	95 (11.0%)	90 (14.6%)	5 (2.04%)
Hypertension	324 (33.7%)	166 (25.2%)	158 (52.3%)	<0.001	962
DM	335 (34.8%)	183 (27.7%)	152 (50.3%)	<0.001	962
CVD	79 (8.21%)	33 (5.00%)	46 (15.2%)	<0.001	962
Chronic lung disease	87 (9.04%)	52 (7.88%)	35 (11.6%)	0.082	962
Chronic kidney disease	43 (4.47%)	21 (3.18%)	22 (7.28%)	0.007	962
Immunocompromised host	16 (1.66%)	10 (1.52%)	6 (1.99%)	0.795	962
Pneumonia	527 (54.8%)	252 (38.2%)	275 (91.1%)	<0.001	962
ARDS	140 (14.6%)	34 (5.15%)	106 (35.1%)	<0.001	962
ICU admission	149 (15.5%)	36 (5.45%)	113 (37.4%)	<0.001	962
ICU duration of stay (number of days [IQR])	13.0 [1.75; 63.8]	13.0 [1.00; 66.1]	13.0 [2.00; 58.0]	0.474	151
Admission to discharge (number of days [IQR])	15.0 [2.00; 52.0]	14.0 [2.00; 39.5]	18.0 [5.00; 60.0]	<0.001	950
Mortality	87 (9.04%)	24 (3.64%)	63 (20.9%)	<0.001	962

Data are presented as counts and percentages (n, %) unless otherwise specified.

SARS-CoV-2 = severe acute respiratory syndrome coronavirus 2; SD = standard deviation; BMI = body mass index; DM = diabetes mellitus; CVD = cardiovascular disease; ARDS = acute respiratory distress syndrome; ICU = intensive care unit; IQR = interquartile range.

Signs and Symptoms

Table 2 summarizes the clinical characteristics of COVID-19 patients at presentation, stratified by anticoagulation category. Patients receiving anticoagulation treatment presented with fever (n = 210 [69.5%]), dyspnea (n = 174 [57.6%]), dry cough (n = 167 [55.3%]), and sore throat (n = 19 [6.3%]).

Table 2.

Signs and Symptoms of SARS-CoV-2 Patients Stratified by Anticoagulation Therapy.

	[ALL]	Anticoagulation = no	Anticoagulation = yes	p-value	N
	N = 962	N = 660	N = 302	p-value	N
Asymptomatic	155 (16.1%)	147 (22.3%)	8 (2.65%)	<0.001	962
Headache	100 (10.4%)	73 (11.1%)	27 (8.94%)	0.376	962
Sore throat	93 (9.67%)	74 (11.2%)	19 (6.29%)	0.023	962
Fever	547 (56.9%)	337 (51.1%)	210 (69.5%)	<0.001	962
Dry cough	459 (47.7%)	292 (44.2%)	167 (55.3%)	0.002	962
Productive cough	68 (7.07%)	42 (6.36%)	26 (8.61%)	0.260	962
SOB	309 (32.1%)	135 (20.5%)	174 (57.6%)	<0.001	962
Fatigue or myalgia	216 (22.5%)	148 (22.4%)	68 (22.5%)	>0.99	962
Diarrhea	113 (11.7%)	76 (11.5%)	37 (12.3%)	0.825	962
Nausea	60 (6.24%)	39 (5.91%)	21 (6.95%)	0.633	962
Vomiting	59 (6.13%)	35 (5.30%)	24 (7.95%)	0.149	962
Change of taste or smell	34 (3.53%)	27 (4.09%)	7 (2.32%)	0.232	962

Data are presented as counts and percentages (n, %) unless otherwise specified. SARS-CoV-2 = severe acute respiratory syndrome coronavirus 2; SOB = shortness of breath.

Laboratory Findings Stratified by Anticoagulation Therapy

Patients receiving anticoagulation therapy had increased white blood cell and neutrophil counts, and creatinine, lactate dehydrogenase, C-reactive protein, procalcitonin, D-dimer, high-sensitivity serum troponin, ferritin, creatinine kinase, alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, gamma-glutamyl transferase, total bilirubin, and direct bilirubin levels, compared to their counterparts. In contrast, patients not receiving anticoagulation therapy had increased levels of hemoglobin and albumin, and lymphocyte count, compared to their counterparts (Table 3).

Table 3.

Baseline Laboratory Parameters of SARS-CoV-2 Patients, Stratified by Anticoagulation Therapy.

	[ALL]	Anticoagulation = no	Anticoagulation = yes	p-value	N
	N = 951	N = 650	N = 301	p-value	N
Hemoglobin (g/L)	127 [125;129]	131 [129;133]	114 [108;119]	<0.001	951
Platelets (10⁹/L)	254 [244;265]	252 [242;262]	259 [237;277]	0.362	950
WBC (10⁹/L)	6.70 [6.50;7.00]	6.30 [6.10;6.50]	8.30 [7.50;9.20]	<0.001	949
Neutrophils count	4.14 [4.00;4.40]	3.70 [3.40;3.83]	6.70 [6.00;7.60]	<0.001	948
Lymphocytes count	1.40 [1.40;1.50]	1.62 [1.60;1.70]	1.00 [0.90;1.10]	<0.001	948
Creatinine (umol/L)	76.0 [75.0;78.0]	74.0 [72.0;76.0]	85.0 [80.0;90.0]	<0.001	945
LDH (IU/L)	305 [290;322]	244 [232;262]	371 [360;398]	<0.001	641
CRP (mg/L)	49.0 [38.0;56.8]	21.0 [17.0;26.0]	102 [91.6;121]	<0.001	907
Procalcitonin (ng/mL)	0.09 [0.08;0.10]	0.07 [0.06;0.07]	0.34 [0.21;0.43]	<0.001	609
D-dimer (ng/mL)	360 [320;402]	256 [247;284]	608 [523;707]	<0.001	617
25 (OH) vitamin D (nmol/L)	41.0 [37.0;44.0]	41.0 [38.0;45.0]	34.0 [29.0;45.0]	0.384	239
Troponin I HS (ng/L)	9.00 [7.00;11.0]	6.00 [5.00;7.00]	16.0 [12.0;21.0]	<0.001	331
Ferritin (ng/mL)	449 [398;496]	316 [289;353]	696 [605;773]	<0.001	595
Creatinine kinase (IU/L)	88.0 [60.0;160]	64.0 [55.0;101]	311 [72.0;3147]	0.004	33
ALT (IU/L)	33.0 [31.0;35.0]	31.5 [29.0;34.0]	36.0 [32.0;41.0]	<0.001	942
AST (IU/L)	33.0 [32.0;35.0]	29.0 [28.0;31.0]	45.0 [41.0;47.0]	<0.001	941
ALP (IU/L)	69.0 [67.0;72.0]	67.0 [65.0;69.0]	78.0 [72.0;86.0]	<0.001	939
GGT (IU/L)	36.5 [33.0;41.0]	30.0 [27.0;33.0]	62.0 [51.0;76.0]	<0.001	802
Albumin (g/L)	35.3 [35.0;35.9]	36.8 [36.1;37.2]	31.0 [30.0;32.0]	<0.001	940
T. bilirubin (umol/L)	11.5 [11.0;11.8]	11.1 [10.6;11.6]	12.1 [11.4;13.0]	0.002	940
D. bilirubin (umol/L)	2.60 [2.40;2.70]	2.20 [2.10;2.30]	3.50 [3.20;4.00]	<0.001	926

Values are presented as median ± interquartile range.

SARS-CoV-2 = severe acute respiratory syndrome coronavirus 2; WBC, white blood cells; LDH, lactate dehydrogenase; CRP, C-reactive protein; HS, high-sensitivity; ALT, alanine aminotransferase; AST, aspartate aminotransferase; ALP, alkaline phosphatase; GGT, gamma-glutamyl transferase; T. bilirubin, total bilirubin; D. bilirubin, direct bilirubin

Treatment Modalities in Hospital

Table 4 summarizes medication prescribed for the study patients, depending on their anticoagulation status. The rates of current use of angiotensin-converting enzyme inhibitors, angiotensin II receptor blockers, and statins were higher in the anticoagulation group than in the non-anticoagulation group. The use of antibiotics (n = 246 [81.5%]), methylprednisolone (n = 101 [33.4%]), dexamethasone (n = 59 [19.5%]), azithromycin (n = 14 [4.6%]), lopinavir-ritonavir (n = 61 [20.2%]), tocilizumab (n = 15 [5%]), and hydrocortisone (n = 18 [6%]) was more common in the anticoagulation group than in the non-anticoagulation group. In contrast, the use of vitamin C effervescent tablets (n = 434 [65.8%]) was more common in the non-anticoagulation group than in the coagulation group. Patients receiving anticoagulation treatment had either high (n = 104 [35.9%]) or low oxygen (n = 147 [50.7%]) requirements; in contrast, patients not receiving anticoagulation treatment had no oxygen requirements (n = 460 [77.1%]).

Table 4.

Medication Prescribed to Patients with SARS-CoV-2, Stratified by Anticoagulation Therapy.

	[ALL]	Anticoagulation = no	Anticoagulation = yes	p-value	N
	N = 962	N = 660	N = 302	p-value	N
Antibiotics	443 (46.0%)	197 (29.8%)	246 (81.5%)	<0.001	962
Methylprednisolone	146 (15.2%)	45 (6.82%)	101 (33.4%)	<0.001	962
Dexamethasone	75 (7.80%)	16 (2.42%)	59 (19.5%)	<0.001	962
Vitamin C effervescent tablets	606 (63.0%)	434 (65.8%)	172 (57.0%)	0.011	962
Azithromycin	18 (1.87%)	4 (0.61%)	14 (4.64%)	<0.001	962
Vitamin D	334 (34.7%)	231 (35.0%)	103 (34.1%)	0.844	962
Hydroxychloroquine	113 (11.7%)	64 (9.70%)	49 (16.2%)	0.005	962
KALETRA (lopinavir/ritonavir)	110 (11.4%)	49 (7.42%)	61 (20.2%)	<0.001	962
ACTEMRA (tocilizumab)	17 (1.77%)	2 (0.30%)	15 (4.97%)	<0.001	962
Hydrocortisone	22 (2.29%)	4 (0.61%)	18 (5.96%)	<0.001	962
Current use of ACE inhibitor	87 (10.5%)	50 (8.38%)	37 (16.2%)	0.002	826
Current use of ARB	110 (13.3%)	57 (9.56%)	53 (23.0%)	<0.001	826
Current use of statin	219 (25.6%)	114 (18.8%)	105 (42.0%)	<0.001	855
OXYGEN requirements:				<0.001	887
High oxygen requirement	139 (15.7%)	35 (5.86%)	104 (35.9%)
Low oxygen requirements	249 (28.1%)	102 (17.1%)	147 (50.7%)
None	499 (56.3%)	460 (77.1%)	39 (13.4%)

The data are presented as counts and percentages (n, %), unless stated otherwise.

SARS-CoV-2 = severe acute respiratory syndrome coronavirus 2; ACE = angiotensin-converting enzyme; ARB = angiotensin II receptor blockers.

Multivariable Logistic Regression Model

Therapeutic anticoagulation agent use (odds ratio [OR] = 2.21, 95% confidence interval [CI], 1.28-3.92, p = 0.005), age (OR = 1.04, 95% CI, 1.02-1.06, p < 0.001), hypertension (OR = 2.30, 95% CI, 1.29-4.17, p = 0.005), COVID-19 pneumonia (OR = 4.86, 95% CI, 1.96-14.75, p = 0.002), and methylprednisolone use (OR = 2.12, 95% CI, 1.25-3.58, p = 0.005) were associated with all-cause cumulative mortality risk (Table 5).

Table 5.

Multivariable Logistic Regression Analysis of Overall in-Hospital Mortality Rates.

		Surviving	Dead	Univariable OR (95% CI, P-value)	Multivariable logistic regression aOR (95% CI, aP-value)
Therapeutic anticoagulation	yes	239 (79.1)	63 (20.9)	6.99 (4.32-11.64, p < 0.001)	2.21 (1.28-3.92, p = 0.005)
Age	Mean (SD)	48.9 (15.4)	63.5 (14.8)	1.06 (1.05-1.08, p < 0.001)	1.04 (1.02-1.06, p < 0.001)
Hypertension	yes	263 (81.2)	61 (18.8)	5.46 (3.41-8.97, p < 0.001)	2.30 (1.29-4.17, p = 0.005)
DM	yes	288 (86.0)	47 (14.0)	2.39 (1.54-3.75, p < 0.001)	0.78 (0.45-1.34, p = 0.371)
Pneumonia	yes	445 (84.4)	82 (15.6)	15.85 (7.04-45.38, p < 0.001)	4.86 (1.96-14.75, p = 0.002)
Fever	yes	485 (88.7)	62 (11.3)	1.99 (1.25-3.29, p = 0.005)	1.50 (0.87-2.64, p = 0.150)
Methylprednisolone	yes	107 (73.3)	39 (26.7)	5.83 (3.64-9.31, p < 0.001)	2.12 (1.25-3.58, p = 0.005)

Multivariable analyses were conducted using logistic regression models utilizing the simultaneous method. The models were adjusted for the characteristics listed in the first column. aOR, adjusted odds ratio; CI, confidence interval; aP-value, adjusted p-value; DM = diabetes mellitus

Mortality Risk

The Cox proportional hazards model revealed that anticoagulation treatment was a significant predictor of mortality (LL = 27.46, df = 1, p < 0.001). At any time, the risk of death among patients not receiving anticoagulation treatment was 70% lower than that among patients receiving this treatment (Table 6). The Kaplan-Meier survival curves yielded consistent findings (Figure 2).

Figure 2.

Kaplan-Meier method-estimated morality rates, stratified by anticoagulation status, depending on time since admission.

Table 6.

Cox Proportional Hazards Regression Coefficients for Anticoagulation.

Variable	B	SE	95% CI	z	p	HR
Anticoagulation = no	−1.20	0.24	[-1.67, -0.72]	-4.93	< .001	0.30

Discussion

This study revealed mean age of the patients receiving therapeutic anticoagulation agents was 57.2 ± 14.6 years. ICU admissions were relatively common in this group. Approximately 36% of the patients receiving therapeutic anticoagulation agents had high oxygen requirements. Overall, 91% of patients in the therapeutic anticoagulation group had pneumonia. Age, hypertension, pneumonia, therapeutic anticoagulation, and methylprednisolone use were found to be strong predictors of in-hospital mortality. In elderly hypertensive COVID-19 patients on therapeutic anticoagulation were found to have 2.3 times higher risk of in-hospital mortality. All cause in-hospital mortality rate in the therapeutic anticoagulation group was up to 21%.

A study by Pawlowski et al found that unfractionated heparin use was associated with higher risk of 28-day mortality.²³ Billett et al showed that apixaban and enoxaparin have comparable mortality risk reducing effects in patients with SARS-CoV-2 infection.²⁴ Meanwhile, the ACTIV-4a trial revealed no survival benefits of therapeutic compared to prophylactic anticoagulation treatment in critically ill SARS-CoV-2 patients.²⁵ The evidence on the prophylactic use of anti-platelets in SARS-CoV-2 patients remains inconclusive.^26–30

The use of anticoagulation agents has been associated with survival benefits in SARS-CoV-2 patients.^31,32 However, intravenous heparin did not improve outcomes in critically ill SARS-CoV-2 patients,³³ and therapeutic anticoagulation was found non-beneficial in many studies.^34,35 Hsu et al reported mortality risk reducing effects of high-intensity anticoagulation treatment in SARS-CoV-2 patients.³⁶ A meta-analysis by Lu et al revealed that the use of antithrombotic medications in SARS-CoV-2 patients did not reduce mortality risks.³⁷ Overall, most studies examining the impact of anticoagulation agent use on mortality risks reported negative findings.^{38, 39} Patients who had outpatient anticoagulation for a period of 90 days were found to have reduced rate of hospitalization.⁴⁰

Limitations

Patients who received anticoagulation therapy in this study had higher prevalence rates of hypertension, DM, cardiovascular disease, and chronic kidney disease; some of these baseline clinical characteristics were independent predictors of COVID-19-related mortality in the population of Kuwait.⁴¹ This study included all SARS-CoV-2-positive patients regardless of disease severity.

Conclusions

In this study age, hypertension, pneumonia, therapeutic anticoagulation, and methylprednisolone use were found to be strong predictors of in-hospital mortality. In elderly hypertensive COVID-19 patients on therapeutic anticoagulation were found to have 2.3 times higher risk of in-hospital mortality. All cause in-hospital mortality rate in the therapeutic anticoagulation group was up to 21%. Further prospective studies are required to elucidate the impact of anticoagulation therapy on in-hospital mortality rates among SARS-CoV-2 patients that meet certain clinical criteria.

Footnotes

Acknowledgments

The authors like to acknowledge Dr Hassan Abdelnaby for his helpful guidance and assistance with sample acquisition. Furthermore, we would like to thank Dr Mohamed Elmetwalli Ghazi, and Dr Danah Alothman for their assistance during the review process.

Statement of Ethics

The study protocol was approved by the standing committee for the coordination of health and medical research at the Ministry of Health in Kuwait (institutional review board number 2020/1422).

Author Contributions

MAR designed the study. MАR and RR раrtiсiраted in data аnаlysis аnd wrote the mаnusсriрt. ААS аnd JР performed the stаtistiсаl аnаlysis and reviewed the mаnusсriрt. The remaining authors collected the data. Аll аuthоrs hаd ассess tо the dаtа аnd took resроnsibility fоr the integrity аnd ассurасy оf dаtа аnаlysis. Аll аuthоrs hаve reаd аnd аррrоved the mаnusсriрt.

Data Availability Statement

The data that support the results of the study are available on request from the corresponding author. The data are not publicly available due to ethical restrictions.

Declaration of Conflicting Interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) received no financial support for the research, authorship, and/or publication of this article.

ORCID iDs

Moudhi Alroomi

Rajesh Rajan

References

Tacquard

Mansour

Godon

, et al. Impact of high-dose prophylactic anticoagulation in critically ill patients with COVID-19 pneumonia. Chest. 2021;159(6):2417‐2427.

Al-Ani

Chehade

Lazo-Langner

. Thrombosis risk associated with COVID-19 infection. A scoping review. Thromb Res. 2020;192:152‐160.

Cui

Chen

Liu

Wang

. Prevalence of venous thromboembolism in patients with severe novel coronavirus pneumonia. J Thromb Haemost. 2020;18(6):1421‐1424.

Helms

Tacquard

Severac

, et al. High risk of thrombosis in patients in severe SARS-CoV-2 infection: a multicenter prospective cohort study. Intensive Care Med. 2020;46(6):1089‐1098.

Klok

Kruip

MJHA

van der Meer

NJM

, et al. Incidence of thrombotic complications in critically ill ICU patients with COVID-19. Thromb Res. 2020;191:145‐147.

Middeldorp

Coppens

Haaps

, et al. Incidence of venous thromboembolism in hospitalized patients with COVID-19. J Thromb Haemost. 2020;18:1995‐2002.

Bilaloglu

Aphinyanaphongs

Jones

Iturrate

Hochman

Berger

. Thrombosis in hospitalized patients with COVID-19 in a New York city health system. JAMA. 2020;324(8):799‐801.

Nadkarni

Lala

Bagiella

, et al. Anticoagulation, bleeding, mortality, and pathology in hospitalized patients with COVID-19. J Am Coll Cardiol. 2020;76:1815‐1826.

Al-Samkari

HGS

Karp Leaf

Wang

, et al. Thrombosis, bleeding, and the effect of anticoagulation on survival in critically ill patients with COVID-19 in the United States. Res Pract Thromb Haemost. 2021;164(5):622‐632.

10.

Ferguson

Volk

Vondracek

Flanigan

Chernaik

. Empiric therapeutic anticoagulation and mortality in critically ill patients with respiratory failure from SARS-CoV-2: a retrospective cohort study. J Clin Pharmacol. 2020;60:1411‐1415.

11.

Paranjpe

Fuster

Lala

, et al. Association of treatment dose anticoagulation with in-hospital survival among hospitalized patients with COVID-19. J Am Coll Cardiol. 2020;76:122‐124.

12.

Tang

Wang

Sun

. Abnormal coagulation parameters are associated with poor prognosis in patients with novel coronavirus pneumonia. J Thromb Haemost. 2020;18(4):844‐847.

13.

Pesavento

Ceccato

Pasquetto

, et al. The hazard of (sub)therapeutic doses of anticoagulants in non-critically ill patients with COVID- 19: the Padua province experience. J Thromb Haemost. 2020;18:2629‐2635.

14.

Dusendang

Schmittdiel

Kavecansky

Tavakoli

Pai

. Anticoagulant and antiplatelet use not associated with improvement in severe outcomes in COVID-19 patients. Blood. 2020;136:59.

15.

Al-Jarallah

Rajan

Saber

AAL

, et al. In-hospital mortality in SARS-CoV-2 stratified by hemoglobin levels: a retrospective study. eJHaem. 2021. doi: 10.1002/jha2.195.

16.

Al-Jarallah

Rajan

Dashti

, et al. In-hospital mortality in SARS-CoV-2 stratified by serum 25-hydroxy-vitamin D levels: a retrospective study. J Med Virol. 2021;93:5880‐5885.

17.

Alroomi

Rajan

Omar

, et al. Ferritin level: a predictor of severity and mortality in hospitalized COVID-19 patients. Immun Inflamm Dis. 2021;9(4):1648‐1655.

18.

Al-Jarallah

Rajan

Dashti

, et al. In-hospital mortality in SARS-CoV-2 stratified by sex diffrences: a retrospective cross-sectional cohort study. Ann Med Surg (Lond. 2022;79:104026. doi: 10.1016/j.amsu.2022.104026. PMID: 35757308; PMCID: PMC9212930.

19.

Mannino

Ford

Redd

. Obstructive and restrictive lung disease and functional limitation: data from the third national health and nutrition examination. J Intern Med. 2003;254(6):540‐547. doi:10.1111/j.1365-2796.2003.01211.x.

20.

Belsky

Tullius

Lamb

Sayegh

Stanek

Auletta

. COVID-19 in immunocompromised patients: a systematic review of cancer, hematopoietic cell and solid organ transplant patients. J Infect. 2021;82(3):329‐338. doi:10.1016/j.jinf.2021.01.022.

21.

Lee

Hwang

Song

, et al. Predication of oxygen requirement in COVID-19 patients using dynamic change of inflammatory markers: CRP, hypertension, age, neutrophil and lymphocyte (CHANeL). Sci Rep. 2021;11:13026. https://doi.org/10.1038/s41598-021-92418-2.

22.

Laine

Reyes

. Tutorial: survival estimation for Cox regression models with time-varying coefficients using SAS and R. J Stat Softw. 2014;61:1‐23.

23.

Pawlowski

Venkatakrishnan

Kirkup

, et al. Enoxaparin is associated with lower rates of mortality than unfractionated Heparin in hospitalized COVID-19 patients. EClinicalMedicine. 2021;33:100774. doi:10.1016/j.eclinm.2021.100774.

24.

Billett

Reyes-Gil

Szymanski

, et al. Anticoagulation in COVID-19: effect of enoxaparin, heparin, and apixaban on mortality. Thromb Haemost. 2020;120(12):1691‐1699.

25.

ATTACC Investigators, ACTIV-4a Investigators, REMAP-CAP Investigators , et al. Therapeutic anticoagulation with heparin in noncritically ill patients with COVID-19. N Engl J Med. 2021;385(9):790‐802.

26.

Nakazawa

Ishizu

. Immunothrombosis in severe COVID-19. EBioMedicine. 2020;59:102942. 2.

27.

Manne

Denorme

Middleton

, et al. Platelet gene expression and function in patients with COVID-19. Blood. 2020;136:1317‐1329.

28.

Goshua

Pine

Meizlish

, et al. Endotheliopathy in COVID- 19-associated coagulopathy: evidence from a single-centre, crosssectional study. Lancet Haematol. 2020;7(8):e575‐e582.

29.

Hottz

Azevedo-Quintanilha

Palhinha

, et al. Platelet activation and platelet-monocyte aggregate formation trigger tissue factor expression in patients with severe COVID-19. Blood. 2020;136(11):1330‐1341.

30.

Chow

Khanna

Kethireddy

, et al. Aspirin use is associated with decreased mechanical ventilation, intensive care unit admission, and in-hospital mortality in hospitalized patients with coronavirus disease 2019. Anesth Analg. 2021;132(4):930‐941.

31.

Fröhlich

Jeschke

Eichler

, et al. Impact of oral anticoagulation on clinical outcomes of COVID-19: a nationwide cohort study of hospitalized patients in Germany. Clin Res Cardiol. 2021;110:1041‐1050.

32.

Ionescu

Jaiyesimi

Petrescu

, et al. Association of anticoagulation dose and survival in hospitalized COVID-19 patients: a retrospective propensity score-weighted analysis. Eur J Haematol. 2021;106:165‐174.

33.

Sadeghipour

Talasaz

Rashidi

, et al. Effect of intermediate-dose vs standard-dose prophylactic anticoagulation on thrombotic events, extracorporeal membrane oxygenation treatment, or mortality among patients with COVID-19 admitted to the intensive care unit: the INSPIRATION randomized clinical trial. JAMA. 2021;325:1620‐1630.

34.

White

MacDonald

Bull

, et al. Heparin resistance in COVID-19 patients in the intensive care unit. J Thromb Thrombolysis. 2020;50:287‐291.

35.

Xue

Zeng

H-Q

, et al. Heparin- binding protein levels correlate with aggravation and multiorgan damage in severe COVID-19. ERJ Open Res. 2021;7(1):00741‐02020.

36.

Hsu

Liu

Zayac

Olszewski

Reagan

. Intensity of anticoagulation and survival in patients hospitalized with COVID-19 pneumonia. Thromb Res. 2020;196:375‐378.

37.

Pan

Zhang

, et al. A meta-analysis of the incidence of venous thromboembolic events and impact of anticoagulation on mortality in patients with COVID-19. Int J Infect Dis. 2020;100:34‐41.

38.

Yin

Huang

Tang

. Difference of coagulation features between severe pneumonia induced by SARS-CoV2 and non-SARS-CoV2. J Thromb Thrombolysis. 2021;51(4):1107‐1110.

39.

Tang

Bai

Chen

Gong

Sun

. Anticoagulant treatment is associated with decreased mortality in severe coronavirus disease 2019 patients with coagulopathy. J Thromb Haemost. 2020;18(5):1094‐1099.

40.

Hozayen

Zychowski

Benson

, et al. Outpatient and inpatient anticoagulation therapy and the risk for hospital admission and death among COVID-19 patients. EClinicalMedicine. 2021;41:101139. doi:10.1016/j.eclinm.2021.101139.

41.

Al Saleh

Alotaibi

Schrapp

, et al. Risk factors for mortality in patients with COVID-19: the Kuwait experience. Med Princ Pract. 2021. doi: 10.1159/000522166

In-hospital Mortality Rates in SARS-CoV-2 Patients Treated with Enoxaparin and Heparin

Abstract

Аbstrасt

Objectives

Methods

Results

Conclusion

Keywords

Introduction

Methods

Study Design and Procedure

Definitions

Stаtistiсаl Anаlysis

Results

Baseline Characteristics

Signs and Symptoms

Laboratory Findings Stratified by Anticoagulation Therapy

Treatment Modalities in Hospital

Multivariable Logistic Regression Model

Mortality Risk

Discussion

Limitations

Conclusions

Footnotes

Acknowledgments

Statement of Ethics

Author Contributions

Data Availability Statement

Declaration of Conflicting Interests

Funding

ORCID iDs

References