Predictors of mortality in COVID-19 patients at Kinshasa Medical Center and a survival analysis: a retrospective cohort study

In December 2019, the first case of coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-COV-2) was detected in China [1]. Three months later, due to its rapid global spread, the World Health Organization (WHO) declared the outbreak a pandemic [1]. By the end of September 2020, the WHO had reported that SARS-COV-2 had infected at least 32.7 million people and was responsible for the deaths of more than one million [2]. The clinical manifestations of this new disease vary widely in severity; ranging from no or mild symptoms to patients with pneumonia progressing rapidly to acute respiratory distress syndrome (ARDS), multi-organ failure and death [3]. There is not only a huge disparity in the severity of this disease but also in its impact globally. From the onset of the pandemic, WHO predicted high morbidity and mortality rates in African countries. However, this has not transpired, with Africa reporting much lower rates than most of the rest of the world [4‐6]. Notwithstanding the huge amount of global research investigating these morbidity and mortality disparities, most of these data emanate from non-African countries.

The Democratic Republic of Congo (DRC) situated in Central Africa, is a vast country with a surface area equivalent to Western Europe with an population of 89,561,403 [4]. The country reported its first case of COVID-19 on March 10, 2020. This was an imported case from France [7]. As of September 27, 2020, there have been a total of 10, 592 positive cases, with a mortality of 271 [2]. To date there is a paucity of research on COVID-19 from the DRC, two papers have been identified. The objective of this study was to identify the factors/determinants for COVID-19 related mortality by comparing the demographic and clinical characteristics of patients diagnosed with COVID-19 admitted to the Kinshasa Medical Center (KMC), located in Kinshasa, the capital of the Democratic Republic of Congo (DRC).

Of 432 consecutive patients with COVID-19 who were admitted to the Hospital Emergency Department at KMC between March 10, 2020 and July 10, 2020, only 106 were hospitalized and followed during the study period (Fig. 1). The baseline characteristics of these 106 patients are summarised in Table 1 and their laboratory findings and chest CT scan score in Table 2. 34 patients died during hospitalisation and 72 were discharged. The mean age of the admitted patients was 55.6 ± 13.2 years, including 26 (24.5%) patients over 65 years old. The majority were male (80.2%) with hypertension being the main comorbidity in 62 (58.2%) patients. The median (IQR) time from COVID-19 symptoms onset to hospital admission was 7 (5.8–10.0) days, whereas the median time to death was 22.0 (14.0–33.0). Fever and cough were the most common initial symptoms (65.1% and 55.7%, respectively). On admission, the median axillary temperature was 37.1 °C (IQR: 36.6–38.3 °C). The median respiratory rate was 22/min (IQR: 20–29/min) and median blood oxygen saturation on room air was 89% (IQR: 82–92%). Compared between the two groups, the patients in non-survivors group had significantly higher age (61.3 ± 12 vs 52.9 ± 13), Systolic Blood Pressure (145.5 ± 17.4 vs 137.0 ± 17), Lactate dehydrogenase (604 [244–874.8] vs 362.5 [228.3–551.8]), HDL cholesterol (1.19 [0.75–1.55] vs 0.85 [0.66–1.08]), troponin (20.8 [10.3–90.5] vs 4.9 [2.0–16.9]), procalcitonin (0.360 [0.185–2.583] vs 0.140 [0.06–0.440]) and lower PaO2/FiO2 ratio (67.6 [57.9–96.5] vs 145.5f [73.1–251.2]). The patients in non-survivors group had also significantly more count of neutrophil (5120.5 [3748–7815] vs 3555.7 [2630–5911.5]) (Table 2). The frequency of complications was higher in non-survivors than survivors (Table 3). The main Complications of the patients included ARDS in 59/66 (89.4%) patients, coagulopathy in 35/93 (37.6%) patients, acute cardiac injury in 24/98 (24.5%) patients, AKI in 15/74 (20.3%) patients and secondary infection in 12/81 (14.8%) patients (Table 3). Only 24 patients were on corticosteroids. All 28 (26.4%) patients who required mechanical ventilation (MV) died. The median time from illness onset to invasive mechanical ventilation was 15 days (9.0–22.0). 14 (13.2%) patients received renal replacement therapy. Some laboratory parameters were tracked from illness onset (Fig. 1). Levels of CRP, PCT and creatinine were clearly elevated in non-survivors compared with survivors throughout the clinical course (Fig. 2). As of July 10, 2020, 34 (32.0%) patients had died; of those that died a total of 17.6% (6/34) had secondary infections. The main bacterial infection found were Staphylococus haemolyticus (Fig. 3). The median (IQR) length of stay from hospitalization to discharge was 18(15–22) days, while the median (IQR) time from hospitalization to death was 22 (14–33) days. Kaplan Meir survival curve of the study population is illustrated in Fig. 4. The median survival time of the entire group was 12 days. The cumulative survival rate of COVID-19 patients was 86.9%, 65.0% and 19.9% respectively at 5, 10 and 20 days. The Kaplan-Meir curves showed a better survival in younger patients, in patients with No AKI and in patients who have a procalcitonin level below 0.5. Patients with no proteinuria and lower respiratory rate at presentation have also a better survival (Fig. 5). Multivariable analysis (Table 4) showed age [aHR 1.38; 95% CI 1.10–1.82], AKI stage 3 [aHR 2.51; 95% CI 1.33–6.80], proteinuria [aHR 2.60; 95% CI 1.40–6.42], RR [aHR 1.42; 95% CI 1.09–1.92] and procalcitonin [aHR 1.08; 95% CI 1.03–1.14] as factors independently associated with an increased risk of mortality.

To date, only two studies have been published from the DRC examining patients admitted with COVID-19 [17, 18]. Both these studies were limited by a lack of robust analysis of biological and laboratory parameters that might predict hospital mortality in COVID-19 [7, 18]. Our retrospective cohort study, carried out in the DRC, aims to add comprehensive data about mortality risk factors for COVID-19. The findings demonstrate that age, respiratory rate, proteinuria, procalcitonin and AKI were significantly associated with mortality in COVID-19 patients. Additionally, increasing levels of creatinine during hospital admission were associated with an increased mortality.

Globally, the hospital COVID-19 mortality rates varies between 4 and 70% [19‐25]. This disparity is partially explained by differences in the epidemiology of the study populations as well as in their hospital management. For example, Du et al. demonstrated that older patients with pre-existent co-morbidities had a higher risk of mortality than a younger healthier person [25]. Ciceri et al. reported 23% mortality in patients presenting less severe forms on admission (a median oxygen saturation of 93%) [26]. In comparison, our study revealed a mortality of 32.0% of whom only 24.5% had an age > 65 years, and had few comorbidities and upon admission had a less severe form of the disease (mean PaO2 62.62 ± 14.0 mmHg). In contrast to international studies demonstrating that being male is associated with an increased risk of mortality [27], our findings did not demonstrate any significant gender difference in risk. All intubated patients died, reflecting the difficulty to manage mechanical ventilation of COVID-19 patients during the first wave in the context of lack of experience and clear recommendations.

As in several previous studies [25‐29], in our study an advanced age was associated with increased mortality from COVID-19. This vulnerability amongst the elderly is often explained by immunoscenescence that is accompanied by a decrease in the production of native T and B cells as well as a decrease in the function of immune cells participating in innate immunity [28]. These changes reduce the effective viral clearance and increase the likelihood of triggering a deregulated immune response in which cytokines are largely released from activated immune cells causing a cytokine storm [28]. In addition to immune senescence, there are several other age-related factors such as comorbidities resulting in higher morbidity and mortality [28]. In our cohort, the number of comorbidities also increased with age.

Viral infections are not usually associated with a raised serum PCT, a finding supported in current COVID-19 research [30]. Procalcitonin, which is the 116-amino acid precursor of the hormone calcitonin, is normally synthetized and released by thyroid parafollicular C cells [30]. It can also be synthetized in many extrathyroid tissues during bacterial infection which is mediated by increased concentration of tumor necrosis factor alpha (TNFα) and interleukin 6 [30]. Worldwide, the average PCT level on admission is less than 0.25 μg/L in COVID-19 patients [31]. During admission for COVID-19, an increased PCT is explained either by a bacterial hospital acquired co-infection or by a general deterioration of the patient [32]. Several studies have reported that elevated PCT is positively associated with the severity of COVID-19 [10, 33‐35]. Hu et al. describe bacterial co-infection rates, defined by a positive blood culture in 20% of those who were severely unwell and in 50% who were critically unwell. Yet, in 50% of those with severe COVID-19 and in 80% of those critically unwell the PCT was raised [30]. In our study, 12/81 (14.8%) of admission blood cultures were positive yet the PCT was raised in 29.5% of those patients. Our study demonstrated that during infection with COVID-19 a progressive elevation of PCT served as a marker for a poor prognosis. This finding was supported by a study by Lippi et al. [36]. Unlike the increase in creatinine, procalcitonin decreases over time in non-survivors and can suggest that the worse outcome of COVID-19 patients in the study may be secondary to organ dysfunction and not superinfection.

Acute Kidney Injury (AKI) affects approximatively 20–40% of COVID-19 patients admitted to intensive care [37]. It is considered as a marker of disease severity and a negative prognostic factor for survival [37, 38]. AKI can lead to impaired acid–base, fluid, and electrolyte homeostasis, all of which may contribute to worse outcomes for patients with COVID-19 [38]. In our cohort the incidence of AKI was 16.2%. A progressive elevation of creatinine was noted as a marker for poor prognosis, yet, only AKI stage 3 was found to be an independent risk factor associated with mortality. AKI is a well-recognised factor of poor prognosis but during the SARS Cov-2 pandemic few studies have found a significant association between AKI and death [37]. This might be explained by the findings of Cheng et al. who demonstrated that only AKI Stages 2 or 3 are associated with a high risk of mortality [39]. Proteinuria is not only a marker for kidney disease or its progression, but also a manifestation of systemic disease in the kidney. Although transient, proteinuria is reported to be a disease severity marker and a mortality risk cause in Intensive care unit (ICU). As in previous studies [40, 41], proteinuria was associated with increased mortality in ICU COVID-19 patients.

Mortality rate of COVID-19 patients is high, particularly in intubated patients and is associated with age, respiratory rate, procalcitonin, proteinuria and acute kidney injury.