Abstract:Hematopoietic stem cell transplant (HSCT) is a curative therapy for malignant and non-malignant conditions. However, complications post-HSCT contribute to significant morbidity and mortality in this population. Acute kidney injury (AKI) is common in the post-allogeneic transplant phase and contributes to morbidity in this population. Continuous renal replacement therapy (CRRT) is used often in the setting of AKI or multiorgan dysfunction in critically ill children. In addition, CRRT can be useful in many disea… Show more
“…This was shown to be 1.46 times more frequent in the treatment group ( n = 19), than in the control group ( n = 13), despite this difference being statistically nonsignificant ( P = .2). It is worth noting that CRRT can sometimes be used in sepsis 34 and for CAR‐T therapy 35 associated cytokine release syndrome with an aim of reducing circulating cytokine levels. Such a rationale might indicate that the higher incidence of CRRT in the fluvoxamine group was a confounding factor which could have assisted in removal of excess cytokines in intervention group patients thus improving their outcomes.…”
Section: Discussionmentioning
confidence: 99%
“…This was shown to be 1.46 times more frequent in the treatment group (n = 19), than in the control group (n = 13), despite this difference being statistically nonsignificant (P = .2). It is worth noting that CRRT can sometimes be used in sepsis 34 and for CAR-T therapy 35 4). Moreover, cytokine removal by means of CRRT remains nonselective, as both pro-and anti-inflammatory cytokines are eliminated, thereby limiting the usefulness of this treatment approach in COVID-19 patients.…”
Aims
Fluvoxamine, a selective serotonin reuptake inhibitor (SSRI) and sigma‐1 receptor agonist, has so far shown promise in the prevention of COVID‐19 progression as an early treatment option in three trials. The aim of this study was to evaluate the safety and efficacy of fluvoxamine in COVID‐19 patients if administered later in the course of the disease.
Methods
The study was designed as an open‐label, prospective cohort trial with matched controls. In April and May 2021, 51 ICU COVID‐19 patients hospitalised in the University Hospital Dubrava and University Hospital Centre Zagreb, Croatia, were treated with fluvoxamine 100 mg three times daily for 15 days in addition to standard therapy and they were prospectively matched for age, gender, vaccination against COVID‐19, disease severity and comorbidities with 51 ICU controls.
Results
No statistically significant differences between groups were observed regarding the number of days on ventilator support, duration of ICU or total hospital stay. However, overall mortality was lower in the fluvoxamine group, 58.8% (
n
= 30/51), than in the control group, 76.5% (
n
= 39/51), HR 0.58, 95% CI (0.36–0.94,
P
= .027).
Conclusion
Fluvoxamine treatment in addition to the standard therapy in hospitalised ICU COVID‐19 patients could have a positive impact on patient survival. Further studies on the effects of fluvoxamine in COVID‐19 patients are urgently required.
“…This was shown to be 1.46 times more frequent in the treatment group ( n = 19), than in the control group ( n = 13), despite this difference being statistically nonsignificant ( P = .2). It is worth noting that CRRT can sometimes be used in sepsis 34 and for CAR‐T therapy 35 associated cytokine release syndrome with an aim of reducing circulating cytokine levels. Such a rationale might indicate that the higher incidence of CRRT in the fluvoxamine group was a confounding factor which could have assisted in removal of excess cytokines in intervention group patients thus improving their outcomes.…”
Section: Discussionmentioning
confidence: 99%
“…This was shown to be 1.46 times more frequent in the treatment group (n = 19), than in the control group (n = 13), despite this difference being statistically nonsignificant (P = .2). It is worth noting that CRRT can sometimes be used in sepsis 34 and for CAR-T therapy 35 4). Moreover, cytokine removal by means of CRRT remains nonselective, as both pro-and anti-inflammatory cytokines are eliminated, thereby limiting the usefulness of this treatment approach in COVID-19 patients.…”
Aims
Fluvoxamine, a selective serotonin reuptake inhibitor (SSRI) and sigma‐1 receptor agonist, has so far shown promise in the prevention of COVID‐19 progression as an early treatment option in three trials. The aim of this study was to evaluate the safety and efficacy of fluvoxamine in COVID‐19 patients if administered later in the course of the disease.
Methods
The study was designed as an open‐label, prospective cohort trial with matched controls. In April and May 2021, 51 ICU COVID‐19 patients hospitalised in the University Hospital Dubrava and University Hospital Centre Zagreb, Croatia, were treated with fluvoxamine 100 mg three times daily for 15 days in addition to standard therapy and they were prospectively matched for age, gender, vaccination against COVID‐19, disease severity and comorbidities with 51 ICU controls.
Results
No statistically significant differences between groups were observed regarding the number of days on ventilator support, duration of ICU or total hospital stay. However, overall mortality was lower in the fluvoxamine group, 58.8% (
n
= 30/51), than in the control group, 76.5% (
n
= 39/51), HR 0.58, 95% CI (0.36–0.94,
P
= .027).
Conclusion
Fluvoxamine treatment in addition to the standard therapy in hospitalised ICU COVID‐19 patients could have a positive impact on patient survival. Further studies on the effects of fluvoxamine in COVID‐19 patients are urgently required.
“…AKI is a relatively common complication after HCT, with a reported incidence rate of 21–84% [ 1 , 2 ]. Table 1 summarizes published studies reporting AKI in the pediatric HCT population [ 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 ].…”
Section: Acute Kidney Injurymentioning
confidence: 99%
“…ICU mortality in children post HCT requiring CKRT is estimated to be 52–65% [ 2 , 49 ]. The 1-year overall survival rate is also poor (27.4% (95% CI: 16–40.5%, p < 0.0001)) [ 1 ].…”
Section: Outcomes Of Krtmentioning
confidence: 99%
“…The 1-year overall survival rate is also poor (27.4% (95% CI: 16–40.5%, p < 0.0001)) [ 1 ]. Reported factors that are associated with mortality include FO > 10%, mechanical ventilation, vasoactive support, and neutropenia at the end of CKRT [ 2 ].…”
Hematopoietic cell transplant (HCT), used for treatment of many malignant and non-malignant pediatric diseases, is associated with serious complications, limiting this therapy’s benefit. Acute kidney injury (AKI), seen often after HCT, can occur at different stages of the transplant process and contributes to morbidity and mortality after HCT. The etiology of AKI is often multifactorial, including kidney hypoperfusion, nephrotoxicity from immunosuppressive and antimicrobial agents, and other transplant-related complications such as transplant-associated thrombotic microangiopathy and sinusoidal obstructive syndrome. Early recognition of AKI is crucial to prevent further AKI and associated complications. Initial management includes identifying the etiology of AKI, preventing further kidney hypoperfusion, adjusting nephrotoxic medications, and preventing fluid overload. Some patients will require further support with kidney replacement therapy to manage fluid overload and AKI. Biomarkers of AKI, such as neutrophil gelatinase-associated lipocalin can aid in detecting AKI before a rise in serum creatinine, allowing earlier intervention. Long-term kidney dysfunction is also prominent in this population. Therefore, long-term follow-up and monitoring of renal function (glomerular filtration rate, microalbuminuria) is required along with management of hypertension, which can contribute to chronic kidney disease.
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