COVID-19 Infection in Transplant Patients

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Overview

Renal transplant patients are under immunosuppression to modulate the immune response to graft. Moreover these patients have various underlying chronic kidney diseases and other co-morbidities such as diabetes and hypertension, which can impact the results in COVID-19 infection. Hence these patients are at a higher risk of developing COVID-19 associated complications.[1] The clinical manifestations, treatment and prognosis of COVID-19 infection may be different from the general population.[2] It is believed that any transplant recipient presented to the infection would result in a high level of cases; however the risk of donor to recipient transmission is unknown. The chances of a donor to recipient infection might be affected by exposure of the donor, infectivity of the the donor during the incubation period and the degree of viremia as well as the viability of virus in specific organ system.Hence, in spite of the conceivable negative outcomes, temporary interruption of kidney transplantation might be needed in regions where the rate of infection is high.[3]

Historical Perspectives

The etiological agent involved is severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), causing coronavirus disease 2019 (COVID-19), first detected in Wuhan, China. On March 12, 2020 the World Health Organization declared the COVID-19 outbreak a pandemic.[4] The earlier SARS epidemic of Hong Kong is known to affect both pediatric and adult renal transplant patients where the severity of disease in adult patients was more than that in pediatric patients[5] The first reported case of COVID-19 infection in renal transplant patient, was a 52‐year‐old man who received living‐related kidney transplantation 12 years for chronic glomerulonephritis, in Wuhan, China. He made a successful recovery and was discharged on day 13.[2]

Classification

Classification of COVID-19 infection in renal transplant patients depends on the severity of COVID-19 manifestations. COVID-19 infection classification according to WHO is following[6]:

Mild Disease Symptomatic patients meeting the case definition for COVID-19

No pneumonia

No hypoxia

Moderate Disease Adolescent or adult

Pneumonia with fever, dyspnea, cough, and fast breathing

SpO2 > or = 90%

Child

Signs of non-severe pneumonia

(cough, difficulty breathing, fast breathing or chest indrawing)

Fast breathing(breaths/min)

<2 months: > or = 60

2-11 months: > or = 50

1-5 years: > or = 40

Diagnosis can be made clinically, Chest Imaging (radiograph, CT scan, Ultrasound) may assist in diagnosis.

Severe Disease Severe Pneumonia Adolescent or adult

Signs of Pneumonia plus one of following:

Respiratory rate > 30 breaths/min

Severe Respiratory Distress

SpO2 < 90%

Child

Pneumonia plus at least one of following

Central cyanosis or SpO2 < 90%

Severe respiratory distress (fast breathing, grunting, severe chest indrawing)

General danger signs such as inability to breastfeed or drink, lethargy, or unconsciousness or convulsions

Fast breathing(breaths/min)

<2 months: > or = 60

2-11 months: > or = 50

1-5 years: > or = 40

Diagnosis can be made clinically, Chest Imaging (radiograph, CT scan, Ultrasound) may assist in diagnosis.

Critical Disease Acute Respiratory Distress Syndrome (ARDS) Onset: within 1 week of pneumonia or new worsening respiratory symptoms.

Chest imaging:

(radiograph, CT scan, or lung ultrasound): bilateral opacities,

not related to volume overload, lobar or lung collapse, or nodules

Origin of pulmonary infiltrates:

Respiratory failure not explained by

cardiac failure or fluid overload.

Oxygenation impairment in adults:

-Mild ARDS: 200 mmHg < PaO2/FiO2a ≤ 300 mmHg (with PEEP or CPAP ≥ 5 cmH2O)

-Moderate ARDS: 100 mmHg < PaO2/FiO2 ≤ 200 mmHg (with PEEP ≥ 5 cmH2O)

-Severe ARDS: PaO2/FiO2 ≤ 100 mmHg (with PEEP ≥ 5 cmH2O)

Oxygenation impairment in children: note OI and OSI.

Use OI when available. If PaO2 not available, wean FiO2 to maintain SpO2 ≤ 97% to calculate OSI or SpO2/FiO2 ratio:

• Bilevel (NIV or CPAP) ≥ 5 cmH2O via full face mask: PaO2/FiO2

≤ 300 mmHg or SpO2/FiO2 ≤ 264.

• Mild ARDS (invasively ventilated): 4 ≤ OI < 8 or 5 ≤ OSI < 7.5.

• Moderate ARDS (invasively ventilated): 8 ≤ OI < 16 or 7.5 ≤ OSI < 12.3.

• Severe ARDS (invasively ventilated): OI ≥ 16 or OSI ≥ 12.3.

Sepsis Adults:

Acute life-threatening organ dysfunction caused by a dysregulated host response to suspected or proven infection. Signs of organ dysfunction: altered mental status, difficult or fast breathing, low oxygen saturation, reduced urine output, fast heart rate, weak pulse, cold extremities or low blood pressure, skin mottling, laboratory evidence of coagulopathy, thrombocytopenia, acidosis, high lactate, or hyperbilirubinemia.

Children

Suspected or proven infection and ≥ 2 age-based systemic inflammatory response syndrome (SIRS) criteria, of which one must be abnormal temperature or white blood cell count.

Septic shock Adults:

Persistent hypotension despite volume resuscitation, requiring vasopressors to maintain MAP ≥ 65 mmHg and serum lactate level > 2 mmol/L

Children:

Any hypotension (SBP < 5th centile or > 2 SD below normal for age) or two or three of the following: altered mental status; bradycardia or tachycardia (HR < 90 bpm or > 160 bpm in infants and heart rate < 70 bpm or > 150 bpm in children); prolonged capillary refill (> 2 sec) or weak pulse; fast breathing; mottled or cool skin or petechial or purpuric rash; high lactate; reduced urine output; hyperthermia or hypothermia

Pathophysiology

Genetics

Angiotensin-converting enzyme 2 and Dipeptidyl peptidase have been implicated in the uptake of SARS-Cov and MERS-CoV[7][8] Several studies have indicated that viral S-protein RBD interacts with host ACE2 receptor. S protein changes thus make the human cells permissive to SARS-CoV and SARS-CoV-2 infection[9] [10] [11] [12] [13]ACE2: ACE ratio is higher in the kidneys compared to the respiratory system. (1:1 in the kidneys VS 1:20 in the respiratory system).[14]These receptors are found in the proximal tubules of kidney[7][8]SARS-CoV2 spike(S) protein is cleaved and activated by transmembrane serine protease family (TMPRSS) after attaching to angiotensin-converting enzyme 2 (ACE2) receptors. This allows the virus to release fusion peptide that aides in membrane fusion..[15]

Associated Conditions

Acute Kidney Injury

  • Pro-inflammatory cytokine levels are elevated in the COVID-19 infection and there is activation of T-cell response. [20]There is higher cytokine levels and there is occurrence of cytokine storm in severe cases. In cytokine storm the, the immune system damages the healthy tissue rather than virus.[21] According to an autopsy report of six patients, the light microscopy indicated CD68+ macrophage infiltration of the tubulointerstitium and severe ATN. The tubules showed complement 5b-9 deposition in all six cases, but deposition in glomeruli and capillaries were seldom seen. Some CD8+ T lymphocyte cells and CD56+ (natural killer) cells were seen in kidney tissue[22]

General COVID-19 Pathophysiology in Renal Transplant Patients

The overall presentation of COVID-19 in renal transplant patients is similar to that in general population[23].However, the renal transplant recipients are at remain at higher risk to catch COVID-19[17] and develop severe complications due to chronic immunosuppressed state which is implicated in various viral infections such as cytomegalovirus, herpes zoster, norovirus infections[24][25]etc.

COVID-19 Pathophysiology

Causes

Life Threatening Causes

Even though the CT findings in COVID-19 pneumonia were similar in renal transplant recipients and general population[26] , due to chronic immunosuppression, the clinical features of COVID-19 in renal transplant patients may be atypical[3] . In one of the study, nine of the 10 patients had fever, cough, shortness of breath, and fatigue; three had diarrhea; eight had lymphopenia; six had renal injury; and six had liver function damage[27] [28] [23] . It needs to be verified whether the severity of COVID-19 pneumonia differs in immunocompromised transplant patients than non-immunocompromised population. According to a report from China’s Infectious Disease Information system, out of 72,314 COVID-19 cases in general population, 81% were reported as mild, whereas 19% were either severe or critical[29] . And, in report from study in renal transplant patients, the number of severe cases were 80% compared to only 10% in their infected family members and 19% in general population[29] .Moreover, average duration of illness was nearly twice i.e. 35 days compared to 18 days in control group and 17-20 days reported in general population.[29][23]


Differentiating type page name here from other Diseases

Epidemiology and Demographics

  • Epidemiological date indicates that the rate of severe complications of COVID-19 is almost 25%, and kidney is also one of the main organs affected in severe illness.[30]
  • AKI is seen in 5-15% of the SARS-CoV and MERS-CoV infection, and the mortality rate is reported to be higher than in general population at 60-90% as per the literature. [31]
  • .The risk is further increased in patients having chronic kidney disease(CKD), patients on chronic replacement therapies, and patients with kidney transplants.[31]
  • In an analysis of 14 articles[32]

[33] [34] [35] [36] [37] [38] [39][40], Median interval of transplantation - 4 years. (range .25-30.1) Fatality rate: 17.4% (4/23)

Age

  • Renal transplant patients of all ages are at a higher risk of COVID-19 due to immunosuppression.
  • The youngest renal transplant patient who died of COVID-19 according to analysis of 14 studies was 71 years old.[32]

[33] [34] [35] [36] [41] [38] [39][40]

  • In general population, COVID-19 associated AKI has higher incidence in elderly.[42]

Gender

  • Men are more likely to be affected by COVID-19 than women.[43]
  • Women dying from COVID-19 are generally elder than men(median age: 82 vs. 79 years for women vs. men, respectively).[43]

Race

*According to study done in New York, 14 recipients (39%) were black, and 15 recipients (42%) were Hispanic.[44]

Risk Factors

There are various factors that can predispose renal transplant patients to COVID-19.

Screening

 
 
 
 
 
 
 
 
 
Patient presents with Sore throat,Dry cough or Fever
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Dysnea, RR>30/min, SpO2<93%
 
If Present Then refer for admission
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Creatinine is raised but no Lymphopenia or No Abnormality on CT chest
 
 
 
If not, check Creatinine, C-RP, CXR & CT chest
 
 
 
Lymphopenia but Creatinine normal and Ct chest normal
 
Admit in usual ward and evaluate Lymphopenia
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Evaluate the Causes of rise in creatinine
 
 
 
Is Xray positive for COVID-19?
 
 
If No, then Do CT Chest
 
If CT Chest is negative then refer patient for Home Care, Medical Treatment, Diagnostic Test, and Daily Follow-ups
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
If Chest Xray or CT chest is indicative of COVID-19 infection: Admit the patient
 
 
 
 
 
 
 
 
 

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Criteria

If available, the diagnostic criteria are provided here.

Symptoms

Presenting symptoms in renal transplant patients are similar to those of non-renal transplant patients.

  • Respiratory symptons
    • Cough
    • Chest Pain
    • Dysnea
  • Fever
  • Hypoxia
  • Lymphopenia
  • High C-Reactive Protein[47]

Valuable prognostic blood tests that can be done are

  • Lymphocyte count
    • Renal transplant patients generally have a low lymphocyte count due to immunosuppression, hence finding a further drop in the lymphocyte count can be of prognostic value.
  • D-dimer
  • Ferritin
  • Troponin
    • Microvascular thrombosis and disseminated intravascular coagulation( with gut ischemia) can occur later in the course of illness. They are characterized by marked increase in the levels of D-dimer particularly. D dimer, ferritin, and troponin should be measured in all patients with severe COVID-19 infection on admission and in those who fail to show any clinical improvement.[47]


Past Medical History

Laboratory Findings

Electrolyte and Biomarker Studies

Electrocardiogram

Chest X Ray

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Pharmacotherapy

Acute Pharmacotherapies

Chronic Pharmacotherapies


Immunotherapy

In renal transplant patients, the immune responses are altered, especially the T cell response, due to generalized immunosuppression. Due to recent timeframe of outbreak of COVID-19 and insufficient scientific evidence, there is limited evidence on decreasing or changing the pattern of immunosuppression in renal transplant patients who have been infected with COVID-19. [48]

  • Clinical presentation of COVID-19 infection in renal transplant patients are like the clinical presentations of infection in general population. [48].Moreover, renal transplant patients are generally immunocompromised, and this predisposes them to severe infection with COVID-19. Rejection of the graft can occur if immunosuppression is reduced in these patients. Hence given the high rate of mortality in COVID-19 infections, it is suggested that a careful risk vs benefits assessment of whether to continue immunosuppression should be done.[49]
  • Managing the immunosuppression in renal transplant patients is difficult and should be based on[49]
    • Age
    • Severity of COVID-19 infection
    • Presence of Co-Morbidities
    • Time since the transplant
  • In patients with mild to moderate infection, it has been a practice to continue or decrease the doses of immunosuppressive drugs, however this approach can cause high mortality in patients having COVID-19 infection.[49]

Immuno Drugs


  • Antiproliferative agents such as MMF and azathioprine [50]
    • Should be stopped at the time of admission to hospital
  • Prednisolone[50]
    • The dosage can be either increased or left unchanged. These can provide immunological protection to the renal graft.
    • Corticosteroids have beneficial effects such as
      • Immunomodulation and anti-inflammatory properties
        • Inhibition of proinflammatory cytokines
        • Reduction of white blood cell traffic
      • Vascular protective effects
        • Maintenance of integrity and permeability of endothelium. [51] [50]
  • Tacrolimus[50]
    • Low doses of tacrolimus can be given but more evidence is required.[50]
    • The dose should be reduced to 50%. Target levels for tacrolimus should be 3-5 ng/ml.[52]
  • Tocilizumab.[50]
    • COVID-19 infection has been found to cause cytokine storm and inflammation due to antiviral immune response, hence trials of anti-interleukin 6 monoclonal antibody Tocilizumab and continuing steroids in infected patients has been considered.
  • Cyclosporine
    • Cyclosporin A has been shown to have an inhibitory effect on proliferation of corona viruses and hepatitis C virus in vitro, not seen in tacrolimus. Cyclosporin A is thought to inhibit the replication of a diverse array of coronaviruses through its impact on cyclophilin A and B.[53][54]
    • Cyclosporine levels should be targeted at 25-50 ng/ml.[52]


Surgery and Device Based Therapy

Indications for Surgery

Pre-Operative Assessment

Post-Operative Management

Transplantation

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

References

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