Systematic Reviews
Copyright ©The Author(s) 2022.
World J Orthop. Nov 18, 2022; 13(11): 1015-1028
Published online Nov 18, 2022. doi: 10.5312/wjo.v13.i11.1015
Table 1 Study characteristics of articles dealing with hepatitis C virus patients undergoing total knee arthroplasty/total hip arthroplasty or other major orthopedic surgery
Author (year)Study designInoculated groups and number of subjectsRisk factors/outcome measuresOutcomesFollow-up
Best (2014)Retrospective cohort study of non-cirrhotic HCV positive individuals and HCV negative patients who underwent TKA/THA in the USA from 1990-2007Group 1: 26444 HCV patients, 14452 subjected to THA (51.2% males) and 11992, to TKA (36.5% males); Group 2: 8336822 HCV negative patients, 2968679 subjected to THA (42.6% males), and 5370202 subjected to TKA (36.2% males)Gender, Age, LOHS, Comorbidities, post-operative bleeding, thrombocytopenia, transfusion reaction, cardiac complications, peripheral vascular complications, urinary complications, acute renal failure, myocardial infarction, pulmonary embolism, pneumonia, deep venous thrombosis, blood transfusion, osteomyelitis, and infectionLOHS, age, rates of total complications, and post-operative bleedingNot specified
Chowdhury (2017)Retrospective registry study with a propensity-matched cohort including HCV patients and uninfected participants who have undergone TKA, THA, and spine procedures in the USA between 2006-2014Group 1: 1131 (52% males) with HCV; Group 2: 95161 (56% males) non-HCV individuals, and after propensity score matching, 1131 non-HCV patients were matched to the HCV group, and the cohort consisted of 2262 patientsMortality within 30- or 90-d, readmission, and complications within 30 and 90 dMortality assessment, complication, and readmission rate evaluationUp to 30 and 90 d post-operatively or upon complication
Pour (2011)Retrospective case-control study with a control group matched at a 2:1 ratio with asymptomatic HCV patients subjected to THA and TKA from 1995-2006 in the USAGroup 1: n = 39 (29 males) HCV patients who have undergone THA; Group 2: n = 80 (60 males) patients who have undergone THA (control group); Group 3: n = 32 (15 males) HCV patients subjected to TKAGroup 4: 64 (30 males) patients subjected to TKA (control group)Αge, gender, BMI, need for transfusion, preoperative PLTS, LOHS, and the complication rateComplication assessment (wound, mechanical, fracture, reoperation, revision); Length of hospital stay101 mo (range 66-140) for the HCV patients subjected to THA; 94 mo (range 45-131 mo) for the control group subjected to THA, 117 months (range 67-150 mo) for the HCV patients subjected to TKA; 98 mo (range 49-133 mo) for the control group subjected to TKA