Absence of negativization of nasal swab test and frailty as risk factors for mortality in elderly COVID-19 patients admitted in long-term care facilities.

METHODS: A limited amount of data is now available on prognostic factors and mortality among elderly people resident in Long-Term Care facilities and in post-acute units. These populations (in particular those with underlying chronic medical conditions) seem to have higher risk of morbidity and mortality related to COVID-19 disease, but further evidence is needed. The aim of our study is to investigate the impact of some well-known prognostic factors in elderly patients (≥ 65 years) with COVID-19 admitted in the Long-Term Care setting in AUSL Ferrara, Italy. We performed binary regression logistic analysis for some variables (demographic data, clinical data including nasal swab test (NST) at discharge and frailty assessments) to find potential predictors of mortality. We subsequently tested statistically significant variables using Kaplan-Meier curves and Cox-regression models to find survival outcomes and related hazard ratio.
RESULTS: Risk factors associated with increased mortality resulted NST at discharge, infection, age and frailty. At a further secondary analysis carried out between NST at discharge, age and clinical frailty scale (CFS) < 5, we found a positive correlation between NST at discharge and CFS < 5. Kaplan-Meier curves showed a statistically significant difference regarding frailty and NST at discharge but not for age.
CONCLUSION: Our study showed that absence of negativization of NST at discharge and frailty are strong predictors for mortality in elderly COVID-19 patients admitted in Long-Term Care facilities, while age and the comorbidity burden are less important.

Aim

A severe respiratory disease was recently reported in Wuhan, Hubei province, China, with the first patient hospitalized on 12 December 2019 [1] and spreaded worldwide, officially being defined as a pandemic by WHO on 11 March 2020 [2]. Clinical severity of infection varies from asymptomatic or mildly symptomatic forms to critical situations with bilateral pneumonia to multiple organ failure [3]. It is crucial to identify prognostic factors related to the most severe forms of disease and mortality. The first data showed a particular vulnerability of the elderly [4, 5]. In fact, older adults have heterogeneous basic clinical conditions and often age and comorbidities do not really reflect the general health status of this kind of patients. For this reason, the concept of “frailty” has been introduced, including different dimensions of performance status and autonomy. Frailty is defined as a condition characterized by a progressive decline in physiological function and by a decrease in strength that leads to greater vulnerability to stress factors, resulting in increased risk of adverse outcomes [6].

Frailty was found to be an independent predictor for death in hospitalized patients with several clinical conditions as well as COVID-19 [7]. Similarly, disability also plays an important role in predicting mortality and adverse outcomes, especially in older people with COVID-19. Deterioration of functional status, as a sign of an augmented vulnerability state and a declining of biological reserves, is generally considered a strong predictor of poor outcome mainly, but not exclusively, in older people [8-10]. Case series have identified age as an independent prognostic factor for mortality. In addition, national registries have shown a high mortality rate among patients older than 80 years [5]. Despite this, studies specifically targeting older patients (≥ 75 years) are few and, though at the highest risk of mortality, information on factors associated with adverse outcome in this population is limited [11]. Similarly, a limited amount of information is available about the natural course of this pandemic and prognostic factors in patients admitted in Long-Term Care facilities [12].

The aim of this paper is to investigate the impact of some well-known prognostic factors in elderly patients (≥ 65 years) with COVID-19 admitted in the Long-Term Care setting in AUSL Ferrara, Italy.

Findings

A total of 471 individuals were admitted between March 2020 and March 2021 in Long-Term Care facilities of the AUSL Ferrara (in particular SS.Annunziata Hospital, Cento and Delta Hospital, Lagosanto). The chosen period includes the first pandemic wave in March 2020 and the second in October 2020. Patients had typical COVID diagnostic criteria: symptoms including respiratory failure and positive nasal swab test (NST) real-time reverse-transcriptase polymerase-chain-reaction (rRT-PCR). All of them were transferred from an Acute Internal Medicine Unit or from an Intensive/Sub-intensive Care Unit, with current or interrupted low-flow O2-support, in order to recover from the illness and improve their functional status. At the time of admission in the Long-Term Care Unit, patients were tested with routine blood sampling and chest X-rays. We recruited in this study 452 patients aged 65 and older, excluding 19 younger patients. Not a single person in our cohort underwent vaccination against Sars-cov2.

The following information were obtained from our computerized medical records and collected from all the individuals included in the study: demographic data (sex, age and residential setting before hospital admission), clinical data (comorbidities expressed with Charlson index, presence of hypertension, diabetes, history of solid or blood tumor, cognitive impairment, endocrinological disorders, obesity, rheumatological, cardiovascular, cerebrovascular, respiratory, hepatic, renal and musculoskeletal disease, necessity of total parenteral nutrition, presence of central venous or urinary catheter, hospital-acquired infections with positive blood cultures requiring antibiotic administration, length of hospital stay and positive/negative NST at discharge), and a frailty pre-admission assessment expressed by clinical frailty scale (CFS) ≥ 5, activities of daily living (ADL) ≤ 2 and polypharmacy (concomitant assumption of ≥ 5 drugs).

We performed NST in our patients at the time of admission and later every 7 days. If a test resulted negative, the patient was discharged. After 21 days of hospitalization, if the test remained positive, the patient was considered recovered from COVID and discharged (according to the decision of our Ministry of Health). Therefore, in our cohort, the number of days of hospitalization almost correspond to the number of days spent with a positive NST.

Patients were divided into two groups, based on the survival outcome from our hospital wards admission (group 1: survived on discharge and group 2: dead on discharge from our hospital wards).

In the descriptive data analysis, continuous variables (age, numbers of drugs, CFS, Charlson index) were expressed as median and standard deviation; p-values were derived using t-test. The categorical and dichotomous variables (sex, comorbidities, ADL < 2, presence of medical devices at admission, NST at discharge and infection during hospitalization) were expressed as absolute values or percentage. P values were obtained using Chi-square test. A p value < 0,05 was considered statistically significant (Table 1).

Table 1

Descriptive analysis and difference between patients discharged alive or dead

		Survived			Dead			Tot
		Avg	330	%	Avg	132	%	Avg	452	p value
Age		82.07			86.52			83.30		< 0.001
Charlson comorbidity index		5.11			4.80			5.02		0.21
CFS		4.66			6.36			5.12		< 0.001
Number of drugs		5.89			5.88			5.88		0.96
Days of hospitalization		22.98			22.65			22.89		0.83
Sex	Female		183	55.5		89	73.0		272	0.001
NST at discharge	Positive		117	35.5		96	78.7		213	< 0.001
Setting of origin	Others than home		72	21.8		57	46.7		129	< 0.001
ADL < 2			103	31.2		84	68.9		187	< 0.001
Venous catheter			43	13.0		22	18.0		65	0.17
Enteral nutrition			3	9		0	0.0		3	0.29
Urinary catheter			84	25.5		36	29.5		120	0.75
Hypertension			245	74.2		82	67.2		327	0.13
Rheumatic disease			25	7.6		9	7.4		34	0.94
Diabetes			79	23.9		31	25.4		110	0.74
Cardiovascular disease			162	49.1		76	62.3		238	0.013
Vasculopathy			142	43.0		49	40.2		191	0.58
Cerebrovascular disease			71	21.5		36	29.5		107	0.076
Respiratory disease			53	16.1		16	13.1		69	0.44
Liver disease			21	6.4		5	4.1		26	0.35
Kidney disease			59	17.9		22	18.0		81	0.97
Musculoskeletal disease			121	36.7		58	47.5		179	0.036
Cancer			88	26.7		28	23.0		116	0.42
Hematological disease			44	13.3		16	13.1		60	0.952
Dementia			150	45.5		82	67.2		232	< 0.001
Endocrinopathy			40	12.1		16	13.1		56	0.776
Obesity			52	15.8		11	9.0		63	0.66
Infection			83	25.2		72	59.0		155	< 0.001

The significante of bold values is referred to the statistical significance of a result (p < 0,05)

CFS clinical frailty scale, ADL activity of daily living, NST nasal swab test

We compared our cohort to the patients admitted to our ward in the previous year (when Sars-cov2 was unknown), finding significant differences. Our cohort showed greater frailty, and this generated longer hospitalization (Table 2).

Table 2

Comparison between 2 years, same hospital ward

	February 2019–February 2020			March 2020–March 2021			p value
	Avg	N	%	Avg	N	%
Over 65		519			452
Sex female		325	62.6		272	60.17	0.6
Days of hospitalization	21.7			22.89			< 0.001
Number of drugs	5.92			5.88			0.78
Charlson	4.95			5.02			< 0.001
CFS	5.22			5.12			0.002
ADL < 2		274	52.8		253	56.0	0.58
Setting of origin (other than home)		211	40.7		129	28.5	0.005
Death		126	24.3		122	26.9	0.33
Male		57	11.0		33	7.3	0.1
Female		69	13.3		89	19.6	0.014

The significante of bold values is referred to the statistical significance of a result (p < 0,05)

To analyze risk factors predicting mortality, a binary logistic regression analysis was performed for dichotomous variables and for continuous variables which were statistically significant at the preliminary analyses (Table 3).

Table 3

Predictors of mortality in COVID-19-positive patients by binary logistic regression model

	Sig	Exp(B)	95% CI Inf	95% CI Sup
Age	.003	1.062	1.021	1.104
CFS	.000	1.519	1.214	1.899
Sex	.156	.659	.371	1.172
NST at discharge	.000	6.662	3.751	11.834
Setting of origin	.331	1.378	.722	2.627
ADL < 2	.204	1.578	.780	3.192
Cardiovascular disease	.108	1.566	.906	2.707
Musculoskeletal disease	.079	1.634	.945	2.825
Dementia	.138	.606	.313	1.175
Infection	.002	2.332	1.351	4.026
Constant	.000	.000

The significante of bold values is referred to the statistical significance of a result (p < 0,05)

CFS clinical frailty scale, ADL activity of daily living, NST nasal swab test

Kaplan–Meier curves (Figs. 1, 2) and Cox-regression models (Table 4) were used to process survival outcomes and related HR resulted statistically significant to binary logistic regression.

Fig. 1

Survival with CFS ≥ 5 (green) or < 5 (blue)

Fig. 2

Survival with positive (green) or negative (blue) nasal swab test at discharge

Table 4

Cox-regression model between overall survival and age, CFS, NST and infection

	Sig	Exp(B)	95% CI Inf	95% CI Sup
Age	.000	1.058	1.029	1.088
CFS	.000	1.320	1.164	1.496
NST at discharge	.000	6.646	4.091	10.795
Infection	.481	1.149	.782	1.688

The significante of bold values is referred to the statistical significance of a result (p < 0,05)

CFS clinical frailty scale; NST nasal swab test

To evaluate any correlation between some significant risk factors for mortality to Cox-regression models (NST at discharge, age and CFS), a further binary logistic regression sub-analysis was performed (Table 5).

Table 5

Predictors of nasopharyngeal swab at discharge in COVID-19-positive patients by binary logistic regression model

	Sig	Exp(B)	95% CI Inf	95% CI Sup
CFS	.002	1.191	1.068	1.327
Age	.594	1.007	.981	1.035

The significante of bold values is referred to the statistical significance of a result (p < 0,05)

CFS clinical frailty scale

All the analyses were processed using SPPS software 21.

Patients consent was not necessary as the data were completely anonymous.

Our cohort of COVID-19-positive patients (452) had a median age of 83.3 years. 59% were female and 122 (27%) died. The mortality rate was 73% in female. Patients who died mostly came from home before being admitted to the acute care ward (53.3%). The average hospital stay was 22.89 days.

Statistically significant differences between the two groups were found for: age (p < 0,001); CFS (p < 0,001); sex (p = 0,001); NST at discharge (p < 0,001); other setting before admission (p < 0,001); ADL < 2 (p < 0,001); cardiovascular disease (p = 0,013); musculoskeletal diseases (p = 0,036); dementia (p < 0,001); infection (p < 0,001) (Table 1).

NST at discharge (OR 6,62; p < 0,001), infection (OR 2,32; p = 0,002), age (OR 1,06; p = 0,003) and frailty (OR 1,51; p < 0,001) represented risk factors associated with increased mortality according to binary logistic regression (Table 3).

Analyzing survival with Kaplan–Meier curves, we detected a statistically significant difference regarding frailty (p < 0,001) and NST at discharge (p < 0,001) (Figs. 1, 2).

The Cox-regression model confirmed these data for age (HR 1,05; p < 0,001), CFS (HR 1,32; p < 0,001) and NST at discharge (HR 6,64; p < 0,001) as well (Table 4).

A further binary logistic regression model between NST at discharge, age and CFS showed a positive relationship between NST at discharge and CFS (OR 1,19; p = 0,002) (Table 5).

Message

In our retrospective observational study on COVID-19 patients admitted in Long-Term Care facilities of the AUSL Ferrara between March 2020 and March 2021, we described population characteristics and looked for predictors of mortality. The mortality rate was 26,9%, with a slight increase, not statistically significant (p value 0,33), compared to the previous year (24,3%), and higher in female population. This is apparently in contrast with literature [13-16], where mortality is higher among men. But the majority of papers refer to acute or intensive care settings [17, 18], while in our paper, we refer to a post-acute setting with a prevalence of female survived patients, burned with greater clinical impairment.

Our study population had an important level of comorbidities (medium Charlson index was 5). In the comparison between dead and survived patients, we found significative some illnesses considered singularly: dementia, obesity, cardiovascular and musculoskeletal disease. These associations were not confirmed with binary analysis in predicting mortality.

In dead group, we found an higher CFS score. In March 2020, the National Institute for Health and Care Excellence (NICE) designed CFS as a first choice in evaluation of frailty in adults patients hospitalized with COVID [19]. We know that frail older adults are more susceptible to a higher risk of developing a severe form of COVID-19, adverse outcomes, mortality and a different response to vaccination for different mechanisms (inflamm-aging, immunosenescence and reduced microbiota diversity) [20]. Our binary and Cox analysis confirmed the link between frailty and mortality regardless of age and comorbidities burden.

According to the literature, age and frailty are strongly linked with mortality [21, 22] and age is considered an absolute risk factor for death in COVID-19 patients [23-26]. We also tried to verify the association between these two variables and found a poor correlation. Moreover, age showed no statistical significance in Kaplan–Meier curve (log rank p = 0,07), confirming that greater age, in the over-65 population, does not correlate with greater mortality and frailty, as confirmed by the other authors [15].

Another interesting result in our analysis was the correlation between mortality and the absence of negativization of NST at discharge. We know that immune response to COVID-19 determines susceptibility to the progression of infection as well as being a major determinant of recovery orchestrated by innate immune and adaptive immune responses [27]. Studies have shown that poor outcomes can be predicted where levels of CD8 + T cells and B cells decrease or CD4 + /CD8 + ratio increases [28, 29]. With aging, we have a shift in T cell subpopulations leading to a decline in naïve T cells and a growth in memory T cells, limiting the response against novel infectious agents [30]. We hypothesized that this immunosenescence is the basis of increased persistence of the virus within the host, which means absence of negativization of NST. This, in our study, was a predictive factor for mortality, correlated with frailty and not with disability or comorbidity burden.

Lastly, we found a correlation with the presence of infection, as confirmed by the other authors [[. Cox analysis did not confirm this correlation, meaning that frailty maintains a key role.

Our study shows that frailty and absence of negativization of NST at discharge are strongly predictive factors for mortality in COVID patients admitted in Long-Term Care facilities, while comorbidities burden and advanced age are less important. Immunosenescence could be an important factor explaining these findings. We underline the crucial role of the comprehensive geriatric assessment and specifically the CFS in clinical and prognostic evaluation in the elderly.

Further studies are needed about NST and Long-Term Care facilities, on which to our knowledge information are lacking. We can probably not generalize our results given the present situation showing different variants of Sars-cov2 and the spreading of vaccination. We hope to see new papers on greater populations, different hospital centers, and considering these new variables.