First author, publication year | Inclusion criteria | Exclusion criteria | Method of quality appraisal or risk of bias |
---|---|---|---|
Munshi, 2019 [31] | ① RCT and observational study; ② Refractory hypoxia in adults with ARDS (including treatments such as inhaled nitric oxide or highfrequency oscillation); ③ MV plus venovenous (VV) ECMO compared with conventional MV; ④ Reported mortality at any time | Main focused venoarterial (VA) ECMO studies | The cochrane riskofbias (ROB) tool and NewcastleOttawa Scale (NOS) |
Shrestha, 2022 [38] | ① Prospective as well as retrospective observational studies and randomized clinical trials; ② Published after 2000; ③ ARDS patients > 18 years of age; ④ Interventions included ECMO (VV/VA or veno arteriovenous (VAV) compared with conventional treatment of MV or other adjunctive therapies; ⑤ Outcomes involving the mortality rate, clinical improvement and recovery, length of hospital stay, adverse effects of ECMO, mean difference of clinical improvement, and healing | ① Comments, editorials, viewpoint articles, systematic reviews, or meta-analyses; ② Non-ARDS patients, less than 18 years of age, or pregnant patients; ③ ECMO used for the management of cases other than ARDS; ④ Not mentioned our outcome of interest | The Cochrane ROB 2.0 tool and the Joanna Briggs Institute (JBI) quality assessment tools |
Tillmann, 2017 [27] | ① Patients > 16 years with severe ARDS as per the Berlin criteria, or classified as having ARDS as per the 1994 American-European Consensus Conference Definition with a PaO2:FiO2 ratio < 100; ② Intervention group received ECMO; ③ Treatment with low tidal volume MV of 8 cm3/kg or less; ④ Reported survival to hospital or ICU discharge | Used ECMO as a pre-specified bridge to lung transplantation | NOS |
Mendes Pedro Vitale, 2019 [30] | ① RCT; ② Adult patients with ARDS; ③ Used ECMO support plus protective MV compared with protective MV alone | Neonatal, pediatric, and experimental data, as well as case series, observational trials and case reports | The Cochrane ROB tool |
Alain Combes, 2020 [32] | ① RCT; ② Published after 2000; ③ Patients with ARDS fulfilling the American-European Consensus Conference definition or the Berlin definition for ARDS; ④ VV ECMO in the experimental group and conventional ventilatory management in the control group | Not mentioned | The Cochrane ROB tool |
Zhu, 2021 [36] | ① Randomized and observational studies; ② Adult populations (age ≥ 18 years old); ③ Comparing ECMO therapy with MV alone in the treatment of severe ARDS; ④ Reported mortality outcomes | ① Animal studies or case reports; ② lacked a comparison group; ③ included patients < 18 years | Modified Jadad scores, the Cochrane ROB tool, or NOS |
Munshi, 2014 [24] | ① ARF patients older than 1 month of age; ② Received ECLS; ③ Compared with patients receiving MV; ④ Reported mortality as an outcome | Not mentioned | The Cochrane ROB tool |
Mitchell, 2010 [22] | ① Controlled trials or cohort studies; ② Reported on the use of ECMO in influenza patients; ③ Included a minimum of 10 patients in each group; ④ Reported comparisons between patients with ARF managed with and without ECMO; ⑤ Reported mortality rates | Neonatal and pediatric studies (patients under 18 years of age) | A nine-point scale combining elements from Jadad’s and Chalmers’ scales |
Alberto Zangrillo, 2013 [23] | ① Reported on 10 or more patients; ② With confirmed or suspected H1N1 influenza infection; ③ Receiving ECMO | ① Reported on fewer than 10 patients treated with ECMO; ② Duplicate publication | NOS |
Alshamsi Fayez, 2020 [34] | ① RCT; ② Adults with ALF or ACLF; ③ Intervention with any form of artificial or bio-artificial ECLS; ④ Control group received supportive care not including ECLS; ⑤ All-cause mortality or liver-related mortality, bridging to liver transplant, improvement of HE and adverse events such as hypotension, bleeding, thrombocytopenia, line infection, and citrate toxicity as outcomes | Not mentioned | The Cochrane ROB tool |
Ouweneel Dagmar, 2016 [26] | ① Diagnosed with either refractory in-hospital or out-of-hospital cardiac arrest or cardiogenic shock after AMI; ② Patients with ECLS support and a control group without ECLS support | ① Case reports, non-human studies, pediatric studies, and reviews; ② not reported on survival to discharge, 30-day outcome or 6-month outcome | A modified version of NOS |
Beyea, 2018 [28] | ① Documented OHCA in adults (age ≥ 16 years); ② Used “ECPR” or equivalent search term, as the intervention; ③ Had either CCPR, defined as either basic life support or advanced cardiovascular life support protocols, or no comparator; ④ Reported hospital outcomes | ① Under age 16 years; ② Cardiac arrests of traumatic etiology, or patients suffered in-hospital cardiac arrest including in the emergency department | NOS |
Twohig, 2019 [29] | ① Observational studies; ② Human adult participants (≥ 17 years old); ③ VA ECMO initiated during cardiac arrest (ECPR); ④ Minimal data outcome of 30-day/hospital mortality reported | ① Languages other than English; ② Traumatic cardiac arrest; ③ Comparator not CCPR (only for ECPR vs. CCPR papers); ④ Minimal data outcome not reported or reported at other later time intervals | The Risk of Bias in Non-randomized Studies of Interventions (ROBINS-I) tool |
Miraglia, 2020 [33] | ① Published in English as full-text articles in indexed journals; ② Used propensity score-matched analysis as part of the study design; ③ Adult participants (≥ 18 years old); ④ Resuscitated from in- and out-of-hospital cardiac arrest; ⑤ Received ECPR; ⑥ Reported neurological outcomes | ① Review articles, opinions, letters, case reports, case series, meta-analyses, and studies reported insufficient data; ② Conducted on pregnancy, pediatric populations, presumed pregnancy, or patients with a pulse (eg, cardiogenic shock) | NOS |
Miraglia, 2020 [35] | ① Employing patient-level randomization or cluster randomization comparing ECPR vs. no ECPR and/or conventional CPR; ② Adults suffering in- or out-of- hospital cardiac arrest, with resuscitation attempted by a bystander or healthcare provider; ③ Compared ECMO using pump-driven VA circuits vs. no ECPR and/or conventional CPR; ④ Long-term neurologically intact survival after in- and out-of- hospital cardiac arrest as the primary outcomes of interest | ① Considering in- or out-of- hospital cardiac arrest in pediatrics and pregnancy; ② considering in- or out-of- hospital cardiac arrest due to trauma, hypothermia, and toxic substances, as the core interventions provided by healthcare providers (CPR and early defibrillation) | ROBINS-I tool |
Scquizzato, 2022 [37] | ① Randomized trials and observational studies reporting propensity score-matched data; ② Comparing adult out-of- hospital cardiac arrest patients treated with ECPR with patients treated with CCPR (i.e., basic and advanced life-support maneuvers) | ① Feasibility studies; ② Enrolling less than 20 patients; ③ Not reporting the primary outcome of survival with favorable neurological outcome | The Cochrane ROB 2.0 tool |
Ahn Chiwon, 2016 [25] | ① Adult patients of cardiac-origin arrest (age 18–75 years); ② Does cardiopulmonary resuscitation with ECMO; ③ Compared to conventional cardiopulmonary resuscitation; ④ Survival rate and neurological outcome as outcomes | ① Comments, reviews, case reports, editorials, letters, conference abstracts, meta-analyses, or animal studies; ② Languages other than English; ③ Duplicate studies; ④ Irrelevant populations; ⑤ Inappropriate controls | The Cochrane ROB tool |