Post by Nadica (She/Her) on Sept 26, 2024 2:44:14 GMT
Preventive interventions for post Covid-19 condition: systematic review update - Preprint Posted Sept 23, 2024
Abstract
Background: Post COVID-19 condition (PCC) can affect individuals regardless of the severity of their initial illness, and its impact on daily life can be significant. There are uncertainties about whether treatments in the acute or post-acute phase of infection can prevent PCC. We report an update to a previous systematic review on the effects of interventions to prevent PCC. Methods: We updated our previous peer-reviewed searches on February 9, 2024. We searched bibliographic databases and grey literature resources to identify trials and comparative observational studies reporting on any intervention provided during the acute (symptom onset to 4 weeks) or post-acute phase (4-8 weeks) of COVID-19 and our primary outcome of incidence of PCC, ascertained at 3 months or longer following infection and capturing, at a minimum, symptoms of fatigue, dyspnea and one or more aspects of cognitive function. Non-recovery from COVID-19 was included if necessary. Secondary outcomes included fatigue, breathlessness/dyspnea, post-exertional malaise, health-related quality of life, psychopathology, cognitive impairment, hospitalization, return to work/education, and adverse effects of the intervention. For screening we employed artificial intelligence to prioritize records and modified our methods to rely on single-reviewer screening after 50% of citations were screened in duplicate. Study selection and risk of bias assessments were conducted independently by two reviewers and data extraction relied on verification of another reviewers work. We grouped studies by intervention type and timing, and by acute-care setting, and performed meta-analysis where appropriate. Sensitivity analyses were conducted for the primary outcome, excluding studies with high risk of bias, using non-recovery as a proxy outcome, and evaluating the outcome at more than 12 months of follow-up. We assessed the certainty of evidence using GRADE. Results: Twenty-four studies (5 randomized and 19 non-randomized), all among adults, were included. The acute care setting in nine studies was outpatient and in 15 studies was in-patient; all but one intervention was administered during the acute-phase of illness. The use of convalescent plasma in outpatient acute COVID-19 care probably does not reduce the risk of PCC (relative risk [RR]: 0.93, 95% CI: 0.77-1.12; 1 RCT; moderate certainty). There was low-certainty evidence suggesting that probiotics (RR [95% CI]: 0.32 [0.13-0.78]; 1 RCT) and metformin (0.50 [0.25-0.99]; 1 RCT among individuals with a BMI >=25 kg/m2) reduce PCC to a small-to-moderate extent in outpatients, while ivermectin (outpatients), antivirals (outpatients), steroids (in-patients), and therapeutic-dose heparin (vs. prophylactic dose; in-patients) may not be effective. Evidence was very low certainty for several other acute-phase pharmacologic intervention and post-acute outpatient assessment and referrals. For outpatient antiviral treatment, while overall PCC risk may not decrease, there might be a slight reduction in psychopathology. Similarly, inpatient antiviral use may not prevent PCC but may offer a small reduction in prolonged general malaise after light exertion. Therapeutic-dose heparin may slightly reduce the risk of cognitive impairment compared to prophylactic-dose heparin among in-patients. The findings remained consistent across all these sensitivity analyses. Conclusions: Evidence suggests that PCC can be prevented to some extent among outpatients with the use of probiotics and metformin during the acute phase of COVID-19. Effects from interventions used among in-patients and within the post-acute phase are uncertain at this time. Evidence on commonly recommended interventions including rehabilitation or multidisciplinary care was lacking. Protocol registration: CRD42024513247
Abstract
Background: Post COVID-19 condition (PCC) can affect individuals regardless of the severity of their initial illness, and its impact on daily life can be significant. There are uncertainties about whether treatments in the acute or post-acute phase of infection can prevent PCC. We report an update to a previous systematic review on the effects of interventions to prevent PCC. Methods: We updated our previous peer-reviewed searches on February 9, 2024. We searched bibliographic databases and grey literature resources to identify trials and comparative observational studies reporting on any intervention provided during the acute (symptom onset to 4 weeks) or post-acute phase (4-8 weeks) of COVID-19 and our primary outcome of incidence of PCC, ascertained at 3 months or longer following infection and capturing, at a minimum, symptoms of fatigue, dyspnea and one or more aspects of cognitive function. Non-recovery from COVID-19 was included if necessary. Secondary outcomes included fatigue, breathlessness/dyspnea, post-exertional malaise, health-related quality of life, psychopathology, cognitive impairment, hospitalization, return to work/education, and adverse effects of the intervention. For screening we employed artificial intelligence to prioritize records and modified our methods to rely on single-reviewer screening after 50% of citations were screened in duplicate. Study selection and risk of bias assessments were conducted independently by two reviewers and data extraction relied on verification of another reviewers work. We grouped studies by intervention type and timing, and by acute-care setting, and performed meta-analysis where appropriate. Sensitivity analyses were conducted for the primary outcome, excluding studies with high risk of bias, using non-recovery as a proxy outcome, and evaluating the outcome at more than 12 months of follow-up. We assessed the certainty of evidence using GRADE. Results: Twenty-four studies (5 randomized and 19 non-randomized), all among adults, were included. The acute care setting in nine studies was outpatient and in 15 studies was in-patient; all but one intervention was administered during the acute-phase of illness. The use of convalescent plasma in outpatient acute COVID-19 care probably does not reduce the risk of PCC (relative risk [RR]: 0.93, 95% CI: 0.77-1.12; 1 RCT; moderate certainty). There was low-certainty evidence suggesting that probiotics (RR [95% CI]: 0.32 [0.13-0.78]; 1 RCT) and metformin (0.50 [0.25-0.99]; 1 RCT among individuals with a BMI >=25 kg/m2) reduce PCC to a small-to-moderate extent in outpatients, while ivermectin (outpatients), antivirals (outpatients), steroids (in-patients), and therapeutic-dose heparin (vs. prophylactic dose; in-patients) may not be effective. Evidence was very low certainty for several other acute-phase pharmacologic intervention and post-acute outpatient assessment and referrals. For outpatient antiviral treatment, while overall PCC risk may not decrease, there might be a slight reduction in psychopathology. Similarly, inpatient antiviral use may not prevent PCC but may offer a small reduction in prolonged general malaise after light exertion. Therapeutic-dose heparin may slightly reduce the risk of cognitive impairment compared to prophylactic-dose heparin among in-patients. The findings remained consistent across all these sensitivity analyses. Conclusions: Evidence suggests that PCC can be prevented to some extent among outpatients with the use of probiotics and metformin during the acute phase of COVID-19. Effects from interventions used among in-patients and within the post-acute phase are uncertain at this time. Evidence on commonly recommended interventions including rehabilitation or multidisciplinary care was lacking. Protocol registration: CRD42024513247