Participant Characteristics
|
All COVID19-positive patients
|
COVID19-positive patients with Radiological Changes of Pneumonia
|
COVID19-positive patients without Radiological Changes of Pneumonia
|
N
|
363
|
294
|
69
|
Age, mean (SD)
|
66.9 (16.7)
|
66.8 (15.4)
|
67.0 (21.5)
|
|
Gender, n (% of column total)
|
Male
|
217 (59.8)
|
185 (62.9)
|
32(46.4)
|
Female
|
146 (40.2)
|
109 (37.1)
|
37 (53.6)
|
|
Ethnicity, n (% of column total)
|
White
|
231 (63.6)
|
179 (61.1)
|
52 (75.4)
|
Asian/Asian British
|
87 (21)
|
75 (25.6)
|
12 (17.4)
|
Black/African/Caribbean
|
26 (7.2)
|
24 (8.2)
|
22 (2.9)
|
Mixed
|
1 (0.3)
|
1 (0.3)
|
0 (0)
|
Other ethnic groups
|
10 (2.7)
|
9 (3.1)
|
1(1.4)
|
Unknown
|
7 (1.9)
|
5 (1.7)
|
2 (2.9)
|
|
Place of admission, n (% of column)
|
Nursing/Residential home
|
47 (12.9)
|
38 (12.9)
|
9 (13.0)
|
Private Residence
|
315 (86.8)
|
255 (86.7)
|
60 (87.0)
|
|
Comorbidity, n (% of column)
|
Chronic kidney Disease
|
105 (28.9)
|
82 (27.9)
|
23 (33.3)
|
Hypertension
|
175 (48.2)
|
150 (51.0)
|
25 (36.2)
|
Type 2 Diabetes Mellitus
|
121 (33.3)
|
102 (34.7)
|
19 (27.5)
|
Dementia
|
32 (8.8)
|
23 (7.8)
|
9 (13.0)
|
Ischaemic Heart Disease
|
70 (19.3)
|
55 (19.7)
|
12 (17.4)
|
|
|
|
|
ITU admission, n (% of column)
|
64 (17.6)
|
61 (20.7)
|
3 (4.3)
|
|
|
|
|
Discharge, n (% of column)
|
245 (67.5)
|
190 (64.6)
|
55 (79.7)
|
|
|
|
|
Mortality, n (% of column)
|
106 (29.2)
|
92 (31.3)
|
14 (20.3)
|
|
Table 1- Population Demographics (Age, Gender and Comorbidities among COVID19 positive patients presenting with and without Radiological Changes within 24 hours of admission
The study population is outlined in table 1 and figure 2. Males (59.8%) were hospitalised more than females (40.2%). The mean age of all patients in this study was 67. Patients of BAME ethnicity were younger (mean-61.85 (14.5)) whilst patients of White ethnicity were older (mean-69.5 (17.3)). Patients of BAME ethincity constituted 31.2% of admissions whilst patients of white ethnicity constituted 63.6% of admissions. Admissions from IMDS 1 and 2 (52.9%) were proportionally similar (figure 2a) to the local Birmingham city population where 56.3% of postcodes are within IMDS 1 and 2 (21). Patients admitted from the highest BHS deprivation indices, 1 and 2, constituted 47.4% of all admissions whilst patients admitted from the highest Living Environment deprivation indices, 1 and 2, constituted 42.4% of all admissions (Figure 2e). 60.2% of BAME patients were populated within the highest BHS deprivation indices, 1 and 2, in comparison to 40.9% of White patients. 69.9% of BAME patients were populated within the highest Living Environment deprivation indices, 1 and 2, in comparison to 50.2% of White patients. Patients admitted from nursing homes (n=47) were all admitted from the top five most deprived BHS deprivation indices.
Patients admitted from regions of highest BHS deprivation, indices 1 and 2, were more likely to be admitted to ITU (OR 2.22, 95% CI 1.111-4.469, p=0.030) in comparison with patients admitted from all other BHS deprivation indices. Patients admitted from regions of highest Living Environment deprivation, indices 1 and 2, were more likely to present with radiological multi-lobar pneumonia (OR 1.923, 95% CI 1.195-3.039, p=0.006) in comparison with patients admitted from all other Living Environment deprivation indices. Patients presenting with radiological multi-lobar pneumonia were more likely to be admitted to ITU (OR 3.174, 95% CI 1.250-8.103, p=0.019) and die (OR 2.224, 95% CI 1.296-3.928, p=0.004).
COVID19 positive patients of BAME ethnicity were more likely to be: admitted from regions of highest BHS deprivation (OR 2.18, 95% CI 1.410-3.445, p<0.001), admitted from regions of highest Living Environment deprivation (OR 2.30, 95% CI 1.450-3.701, p<0.001), present with radiological pneumonia (OR 2.31 95% CI 1.249-4.394, p=0.008), present with multi-lobar pneumonia (OR 2.480, 95% CI 1.446-4.172, p<0.001) than patients of white ethnicity (figure 3a).
Furthermore, COVID19 positive patients who were admitted to ITU were more likely to: be of BAME ethnicity (OR 3.5 95% CI 2.00-6.06, p<0.001), be admitted from regions of highest BHS deprivation (OR 2.22, 95% CI 1.111-4.469, p=0.030), present with radiological pneumonia (OR 4.880, 95% CI 1.452-16.14, p=0.008) and present with multi-lobar pneumonia (OR 3.174, 95% CI 1.250-8.103, P=0.019) than COVID19 positive patients who were not admitted to ITU (figure 3b).
Moreover, COVID19 positive patients who died were more likely to: be admitted from a nursing/residential home (OR 4.729, 95% CI 2.533 – 8.922, p<0.001), present with radiological pneumonia (OR 4.880, 95% CI 1.452-16.14, p=0.008), present with multi-lobar pneumonia (OR 2.224, 95% CI 1.296-3.928, p=0.004), present with increased severity, present with CURB 65 ≥ 3, (OR 5.32, 95% CI 3.267-8.662, p<0.001), and have been admitted to ITU during the inpatient stay (OR 14.57, 95% CI 5.089-36.85, P<0.001) than patients who were discharged (figure 3c).
Individual comorbidities were significantly associated with increased risk of death among hospitalised COVID19 positive patients: hypertension (OR-1.806, 95% CI 1.129-2.864, p=0.014), ischaemic heart disease (OR-2.096, 95% CI 1.204-3.625, p=0.011), diabetes mellitus (OR 1.67 95%CI 1.046-2.650, p=0.037) dementia (OR-3.375, 95% CI 1.657-7.314, p=0.002) and chronic kidney disease (OR-2.36, 95% CI 1.452-3.841, p=0.001) (figure 4). Charlson Comorbidity Scores were higher among COVID19 positive patients who died (Median 6 (IQR 4)) in comparison with patients who were discharged (Median 3 (IQR 5), p<0.001). Patients with higher Charlson Comorbidity Scores, presented with increased severity, CURB 65, (p<0.001). Charlson Comorbidity Index Scores were higher among patients of white ethnicity in comparison to patients BAME ethnicity (White- median 5 (IQR 5), BAME-median- 3 (IQR 4.75), p=0.002). Patients of White ethnicity were more likely to present with increased severity on admission, CURB65 ≥ 3, (OR 2.15, 95% CI 1.306-3.39, p=0.0023) in comparison to patients of BAME ethnic origin. Charlson Comorbidity Scores were also higher among patients admitted from nursing/residential homes in comparison with patients admitted from a private residence (Nursing/Residential home - Median 6 (IQR 3), Private residence- Median 4 (IQR 4), p=0.001). Patients admitted from nursing/residential homes were more likely to present with increased severity on admission, CURB65 ≥ 3, (OR 5.016, 95% CI 2.656-9.385, p<0.001) in comparison to patients admitted from a private residence.
Clinical Frailty Scores were higher among COVID19 positive patients who died (median-6.00 (IQR-3.50) in comparison to COVID19 positive patients who survived (median-3.00 (IQR-3.00), p<0.001). Patients admitted from Nursing/Residential homes had higher Clinical Frailty Scores than patients admitted from a private residence (Nursing/Residential home - Median 7 (IQR 1), Private residence- Median 3 (IQR 3), p<0.001). There is no statistical significance in Clinical Frailty Score between patients of BAME and White ethnic origin (BAME: median-3(IQR-4), White: median-4 (IQR-4), p=0.188).
Exploring the profiles of social determinants of health among patients clustered by outcome and deprivation (BHS and LE deprivation respectively)
Two two-step cluster analyses were undertaken to identify homogenous clusters based on:
(A) BHS deprivation and completed hospital episode outcome (n=344) and (B) LE deprivation and completed hospital episode outcome (n=344). Within each analysis four distinct clusters emerged reflecting four statistically distinct groups (table 2):
(A) Two step cluster analysis “A” clustering hospitalised COVID19 positive patients by BHS deprivation and completed hospital episode outcome
Cluster A1 is characterised by patients admitted from regions of highest BHS deprivation, indices 1-2, who died. Cluster A2 is characterised by patients admitted from all other BHS deprivation indices who died. Cluster A3 is characterised by patients admitted from regions of highest BHS deprivation, indices 1-2, who were discharged. Cluster A4 is characterised by patients admitted from all other BHS deprivation indices who were discharged.
(B) Two step cluster analysis “B” clustering hospitalised COVID19 positive patients by LE deprivation and completed hospital episode outcome
Cluster B1 is characterised by patients admitted from regions of highest LE deprivation, indices 1-2, who died. Cluster B2 is characterised by patients admitted from all other LE deprivation indices who died. Cluster B3 is characterised by patients admitted from regions of highest LE deprivation, indices 1-2, who were discharged. Cluster B4 is characterised by patients admitted from all other LE deprivation indices who were discharged.
Clusters A1 and B1 had relatively high proportions of: BAME patients, comorbidities among patients (chronic kidney disease, dementia, ischaemic heart disease, hypertension and type 2 diabetes mellitus) and admissions from nursing/residential homes in comparison to the corresponding proportions among all patients.
Clusters A2 and B2 had relatively high proportions of: white patients, comorbidities among patients (chronic kidney disease, dementia, ischaemic heart disease, hypertension and type 2 diabetes mellitus) and admissions from nursing/residential homes in comparison to the corresponding proportions among all patients.
Clusters A3 and B3 had a relatively high proportion of BAME patients but relatively lower proportions of: comorbidities among patients (chronic kidney disease, dementia, ischaemic heart disease, hypertension and type 2 diabetes mellitus) and admissions from nursing/residential homes in comparison to the corresponding proportions among all patients.
Clusters A4 and B4 had a relatively high proportion of white patients but relatively lower proportions of: comorbidities among patients (chronic kidney disease, dementia, ischaemic heart disease, hypertension and type 2 diabetes mellitus) and admissions from nursing/residential homes in comparison to the corresponding proportions among all patients.
Table 2 shows the cluster membership profiles in relation to: age, gender, ethnicity, place of admission, comorbidities, Charlson Comorbidity Index and Clinical Frailty Score. Figure 5a shows a graphical representation of individual comorbidity profiles within each of the four emergent clusters from a two-step cluster analysis clustering hospitalised COVID19 positive patients by BHS deprivation and hospitalised episode outcome. Figure 5b shows a graphical representation of individual comorbidity profiles within each of the four emergent clusters from a two-step cluster analysis clustering hospitalised COVID19 positive patients by LE deprivation and hospitalised episode outcome. Group comparisons were performed to examine the profiles of independent comorbidities, Charlson Comorbidity Scores and Clinical Frailty Scores.
Examining comorbidities within clusters
Charlson Comorbidity Index scores for patients who died were above the average for all patients (Median-4.00, IQR-4.00), irrespective of deprivation ; this was regardless of whether patients were admitted from indices of highest BHS and LE deprivation respectively (Cluster A1; Median-6.00, IQR-5.00, Cluster B1; Median- 6.00, IQR-4.00) or all other BHS and LE deprivation indices respectively (Cluster A2; Median-6.00, IQR-3.00, Cluster B2; Median- 6.00, IQR-4.75). Patients who were discharged from hospital had Charlson Comorbidity Index scores around/below the average for all patients in indices of highest BHS and LE deprivation respectively (Cluster A3; Median-2.00, IQR-4.00, Cluster B3; Median-3.00, IQR-4.25) and all other BHS and LE deprivation indices respectively (Cluster A4; Median-4.00, IQR-4.00, Cluster B4; Median-3.00, IQR-4.00). There was a statistically significant difference between the cluster A medians (p<0.001) and the cluster B medians (p<0.001).
Irrespective of BHS deprivation, among patients who died (Clusters A1 and A2), there was no statistically significant difference in comorbidities: chronic kidney disease (p=0.158), dementia (p=0.304), ischaemic heart disease (p=1.000), hypertension (p=0.413), type 2 diabetes mellitus (p=1.000). Furthermore, irrespective of LE deprivation, among patients who died (Clusters B1 and B2), there was no statistically significant difference in comorbidities: chronic kidney disease (p=0.840), dementia (p=0.793), ischaemic heart disease (p=0.376), hypertension (p=0.536), type 2 diabetes mellitus (p=0.411).
Among COVID19 positive patients admitted from the most deprived BHS indices (cluster A1 and A3), patients who died were more likely to have: chronic kidney disease (OR 2.619, 95% CI 1.180-5.697, p=0.0253), dementia (OR 6.525, 95% CI 2.021-18.16, p=0.001) and ischaemic heart disease (OR 2.813, 95% CI 1.242-6.611, p=0.028) but were not more likely to have hypertension (p=0.359) or type 2 diabetes mellitus (p=0.450) in comparison to patients who were discharged. Furthermore, among COVID19 positive patients admitted from the most deprived LE indices (cluster B1 and B3), patients who died were more likely to have: chronic kidney disease (OR 2.408, 95% CI 1.314-4.443, p=0.0063), dementia (OR 4.950, 95% CI 1.725-13.21, p=0.0042) and ischaemic heart disease (OR 3.111, 95% CI 1.505-6.185, p=0.0024) but were not more likely to have hypertension (p>0.05) or type 2 diabetes mellitus (p=0.084) in comparison to patients who were discharged.
Examining frailty within clusters
Clinical Frailty Scores for patients who died were above the average for all patients (Median 4.00, IQR-4.00), irrespective of deprivation ; this was regardless of whether patients were admitted from indices of highest BHS and LE deprivation respectively (Cluster A1; Median-6.00, IQR-4.00, Cluster B1; Median-6.00, IQR-3.50) or from all other BHS and LE deprivation indices respectively (Cluster A2; Median-6.00, IQR-3.00, Cluster B2; Median-5.50, IQR-4.00). Patients who were discharged from hospital had Clinical Frailty Scores around/below the average for all patients, irrespective of deprivation, in indices of highest BHS and LE deprivation respectively (Cluster A3; Median-3.00, IQR-3.00; Cluster B3; Median-3.00, IQR-4.00) and all other BHS and LE deprivation indices respectively (Cluster A4; Median-4.00, IQR 4.00, Cluster B4; Median-4.00, IQR-3.00). There was a statistically significant difference between the cluster A medians (p<0.001) and the cluster B medians (p<0.001).
|
All patients
|
(A) Four emergent clusters from a two-step cluster analysis “A” clustering COVID19 positive patients by BHS deprivation and completed hospitalised episode outcome
|
(B) Four emergent clusters from a two-step cluster analysis “B” clustering COVID19 positive patients by LE deprivation and completed hospitalised episode outcome
|
Cluster A1 Highest BHS deprivation indices and died
|
Cluster A2 All other BHS deprivation indices and died
|
Cluster A3 Highest BHS deprivation indices and discharged
|
Cluster A4 All other BHS deprivation indices and discharged
|
Cluster B1
Highest LE deprivation indices and died
|
Cluster B2
All other LE deprivation indices and died
|
Cluster B3
Highest LE deprivation indices and discharged
|
Cluster B4
All other LE deprivation indices and discharged
|
n
|
344
|
41
|
64
|
118
|
121
|
67
|
38
|
131
|
108
|
Age (Mean (SD) )
|
67.2 (18.4)
|
69.9 (14.3)
|
79.8 (12.0)
|
59.3 (17.2)
|
67.5 (15.0)
|
76.5 (13.4)
|
75.0 (14.6)
|
60.8 (15.9)
|
66.5(17.1)
|
|
Gender (n (% within column))
|
Male
|
202 (58.7)
|
25 (61.0)
|
39 (60.9)
|
74 (61.2)
|
64 (54.2)
|
44 (65.6)
|
20 (52.6)
|
67 (51.1)
|
71 (65.7)
|
Female
|
142 (41.3)
|
16 (39.0)
|
25 (39.1)
|
47 (38.8)
|
54 (45.8)
|
23 (34.3)
|
18 (47.4)
|
41 (31.3)
|
60 (55.6)
|
|
Ethnicity (n (% within column))
|
BAME
|
113 (32.8)
|
19 (48.7)
|
14 (22.2)
|
47 (40.2)
|
33 (28.2)
|
28 (41.8)
|
5 (13.2)
|
51 (38.9)
|
29 (26.9)
|
White
|
223 (64.8)
|
20 (51.3)
|
49 (77.8)
|
70 (59.8)
|
84 (71.8)
|
36 (53.7)
|
33 (86.8)
|
77 (58.8)
|
77 (71.3)
|
|
Place of Admission (n (% within column))
|
Nursing/Residential home
|
47 (13.7)
|
9 (22.0)
|
20 (31.3)
|
5 (4.2)
|
13 (10.7)
|
14 (20.9)
|
15 (39.5)
|
9 (6.9)
|
9 (8.3)
|
Private Residence
|
297 (86.3)
|
32 (78.0)
|
44 (68.8)
|
116 (98.3)
|
105 (86.8)
|
53 (79.1)
|
23 (60.5)
|
122 (93.1)
|
99 (91.7)
|
|
Comorbidities (n (% within column))
|
Chronic Kidney Disease
|
103 (29.9)
|
14 (34.1*,+ )
|
32 (50.0*)
|
20 (16.5+)
|
37 (31.4)
|
30 (44.8^,-)
|
16 (42.1 ^)
|
33 (25.2-)
|
24 (22.2)
|
Dementia
|
32 (9.3)
|
9 (22.0*,+)
|
9 (14.1*)
|
5 (4.1+)
|
9 (7.6)
|
11 (16.4^,-)
|
7 (18.4 ^)
|
5 (3.8-)
|
9 (8.3)
|
Ischaemic Heart disease
|
69 (20.1)
|
12 (30.0*,+)
|
19 (29.7*)
|
16 (13.2+)
|
22 (18.8)
|
22 (32.8^,-)
|
9 (23.7 ^)
|
18 (13.7-)
|
20 (18.5)
|
Hypertension
|
164 (47.7)
|
21 (52.5*)
|
40 (62.5*)
|
51 (42.9)
|
52 (44.8)
|
41 (61.2^)
|
20 (52.6 ^)
|
59 (45.0)
|
44 (40.7)
|
Type 2 Diabetes Mellitus
|
116 (33.7)
|
16 (39.0*)
|
26 (40.6*)
|
39 (32.2)
|
35 (29.7)
|
29 (43.3^)
|
13 (34.2^)
|
40 (30.5)
|
34 (31.5)
|
|
Charlson Comorbidity Index (Median (IQR))
|
4.00 (4.00)
|
6 (5.00)
|
6 (3.00)
|
2 (4.00)
|
4 (4.00)
|
6 (4.00)
|
6.00 (4.75)
|
3.00 (4.25)
|
3.00 (4.00)
|
|
Clinical Frailty Score (Median (IQR))
|
4.00 (4.00)
|
6 (4.00)
|
6 (3.00)
|
3 (3.00)
|
4 (4.00)
|
6 (3.50)
|
5.50 (4.00)
|
3.00 (4.00)
|
4.00 (3.00)
|
|
Table 2- Cluster membership profiles in relation to: age, gender, ethnicity, place of admission, comorbidities, Charlson Comorbidity Index and Clinical Frailty Score. Cluster membership profiles are of the four emergent clusters from two two-step cluster analyses which were carried out clustering hospitalised COVID19 positive patients by: (a) BHS deprivation and completed hospitalised episode outcomes and (b) LE deprivation and completed hospitalised episode outcome.
*among patients who died, there is no statistical significance in the respective comorbidity profiles between patients admitted from indices of highest BHS deprivation and all other BHS deprivation indices.
+among patients admitted from indices of highest BHS deprivation, there is a statistical significance in the respective comorbidity profiles between patients who died and those who were discharged.
^among patients who died, there is no statistical significance in the respective comorbidity profiles between patients admitted from indices of highest LE deprivation and all other LE deprivation indices.
-among patients admitted from indices of highest LE deprivation, there is a statistical significance in the respective comorbidity profiles between patients who died and those who were discharged.