To the Editor,The global overload that health systems are undergoing since the start of the COVID‐19 pandemic has forced hospitals to explore sustainable alternatives to treat vulnerable patients that require closer monitoring and higher use of resources, such as Kidney Transplant Recipients (KTRs).
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The use of telemedicine and hospital‐like infrastructures represent a valid option for most patients with mild‐moderate COVID‐19, as well as for patients in the recovery phase who cannot be discharged from hospital.
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Herein, we present our experience with KTRs infected by SARS‐CoV‐2 in the Hotel Salut (Health Hotel, HH), which was set‐up within 2.5 km from the Hospital on March 25, 2020, coinciding with the main COVID‐19 outbreak in Spain. At full capacity, the HH could accommodate up to 300 patients across 6 floors of 50 single‐rooms each floor. The HH was equipped with both human and material resources from the Hospital Clínic of Barcelona, including 24‐hour medical and nurse attention, availability of high‐flux oxygen, a pharmacy and the same IT equipment.By the end of May, 45 KTRs who were followed‐up at our center developed COVID‐19, of which 28 were hospitalized at the Hospital Clínic. Twelve patients were transferred to the HH according to the following criteria: (a) >6 days from symptoms onset, (b) temperature below 37.3°C, iii) Respiratory rate < 22 per minute and FiO2 < 0.35, iv) C‐Reactive Protein < 5 mg/dL or descending, LDH < 240 UI/L or descending, lymphocytes > 1000/mm3 or increasing, and v)without radiological progression. Baseline characteristics and treatment are highlighted in Table 1 and are described as median [interquartile range], frequencies, and percentages. Differences were explored the with Mann–Whitney test or Fisher's exact test with SPSS 25.0 (SPSS Inc). The study has been approved by the local Ethical Committee (code HCB/2020/0641). The treatment protocol used in the HH was the same as the one carried out in the Hospital, and already described by our group.
Mycophenolate and/or mTOR inhibitors were discontinued in all patients. Calcineurin inhibitors were also suspended in case lopinavir/ritonavir was prescribed. KTRs were transferred to HH after 8.0 [4.25‐13.50] days of hospitalization; at that stage none of them had fever and 20% were still needing oxygen. Hospital stay was significantly shorter for patients treated at HH than for those discharged directly from the hospital (12.50 [8.25‐19.50] days, P = .001). Median stay at the HH was 9.50 [6.50‐12.50] days, and only one patient was readmitted to the Hospital for respiratory deterioration 3 days after HH admission, being discharged from the hospital 9 days afterward. Evolution of clinical parameters reflected progressive recovery after infection (Figure 1). It should be noted that stay at HH also allowed the gradual reintroduction of immunosuppression despite the challenging interactions between calcineurin inhibitors (CNIs) and the antiviral agents.
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Therefore, tacrolimus was restarted 9 [8‐ 11] days after withdrawal, with trough levels of 4.85 [3.92‐5.55]ng/mL at the time of HH discharge. The rest of immunosuppressant drugs were introduced gradually afterward, tapering the steroids simultaneously.
Table 1
Baseline characteristics and treatment of KTRs total population. Comparison between KTRs who were transferred to the Hotel Salut (Health Hotel, HH) and those who were discharged directly from the Hospital
Total population
(n = 28)
Transferred
to HH
(n = 12)
Discharged from
the Hospital
(n = 16)
P‐value
Age
52.50 [46.25‐68]
48.50 [43.75‐57.25]
58 [47.25‐72.75]
.110
Sex (% males)
18/28 (64.3%)
7/12 (58.3%)
11/16 (68.8%)
.698
Time from transplant
56.46 [22.01‐125‐45]
42.56 [12.21‐74.75]
65.15 [26.11‐134.92]
.423
Baseline immunosuppression
TAC + MPA
14/28 (50.0%)
5/12 (41.7%)
9/16 (56.3%)
.240
TAC + mTORi
9/28 (32.1%)
6/12 (50.0%)
3/16 (18.8%)
Other
5/28 (17.9%)
1/12 (8.3%)
4/16 (25.0%)
Creatinine at baseline (mg/dL)
1.55 [1.15‐2.18]
1.93 [1.44‐2.54]
1.29 [1.13‐2.10]
.093
Positive PCR swab (%yes)
23/28 (82.1%)
9/12 (75.0%)
14/16 (87.5%)
.624
Symptoms (%yes)
Fever
26/28 (92.9%)
10/12 (83.3%)
16/16 (100.0%)
.175
Cough
18/28 (64.3%)
9/12 (75.0%)
9/16 (56.3%)
.434
Dyspnea
9/28 (32.1%)
2/12 (16.7%)
7/16(43.8%)
.223
Gastrointestinal
7/28 (25.0%)
2/12 (16.7%)
5/16 (31.3%)
.662
Dysgeusia
3/28 (10.7%)
1/12 (8.3%)
2/16 (12.5%)
1
Pneumonia
25/28(95.3%)
9/12 (75.0%)
16/16 (100.0%)
.067
AKI
19/28 (67.9%)
9/12 (75.0%)
10/16 (62.5%)
.687
Need of dialysis
3/28 (10.7%)
0/12 (0.0%)
3/16 (18.8%)
.238
Treatment
Lopinavir/Ritonavir
24/28 (85.7%)
9/12 (75.0%)
15/16 (93.8%)
.285
Hydroxicloroquine
27/28 (96.4%)
12/12 (100.0%)
15/16 (93.8%)
1
Azithromycin
27/28 (96.4%)
11/12 (91.7%)
16/16 (100.0%)
.429
Tocilizumab
18/28 (64.3%)
6/12 (50.0%)
12/16 (75.0%)
.243
Steroids (bolus)
8/28 (28.6%)
3/12 (25.0%)
5/16 (31.3%)
1
ICU Admission
8/28 (28.6%)
3/12 (25.0%)
5/16 (31.3%)
1
Death
5/28 (17.9%)
0/12 (0.0%)
5/16 (31.3%)
.053
Length of stay
At the Hospital
12.50 [8.25‐19.50]
8 [4.25‐13.50]
15.50 [12‐25.50]
.001
At the Hotel
/
9.50 [6.50‐12.50]
/
Total
18 [13‐24]
19.00 [16.25‐24]
15.50 [12‐25.50]
.631
Figure 1
Evolution of COVID‐19‐related laboratory parameters before and after HH admission
Baseline characteristics and treatment of KTRs total population. Comparison between KTRs who were transferred to the Hotel Salut (Health Hotel, HH) and those who were discharged directly from the HospitalTotal population(n = 28)Transferredto HH(n = 12)Discharged fromthe Hospital(n = 16)Evolution of COVID‐19‐related laboratory parameters before and after HH admissionIn conclusion, although our study was conducted among a small proportion of all the COVID‐19 infected KTRs, treating them at a medicalized hotel facility allowed us to monitor their progress closely, thus obtaining positive clinical outcomes as well as the ability to safely reintroduce immunosuppression.
CONFLICT OF INTEREST
The authors of this manuscript have no conflicts of interest to disclose as described by Clinical Transplantation.
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