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Table 5 Linear regression analysis of total follow-up

From: Fully digital data processing during cardiovascular implantable electronic device follow-up in a high-volume tertiary center

 

Regression coefficient

95% confidence interval

p value

Intercept

20.21

(15.31; 25.11)

< 0.001

FDDP use (vs. conventional follow-up)

− 0.63

(− 2.22; 0.96)

0.439

Female gender (vs. male)

− 0.82

(− 2.27; 0.64)

0.273

Age (per year)

0.03

(− 0.02; 0.08)

0.261

Concomitant cardiac disease

1.41

(− 0.46; 3.27)

0.141

Physician experience in clinical EP (per year)

− 1.07

(− 1.39; -0.75)

< 0.001

Device type

0.009

Single chamber P (vs. CRT-P/CRT-D)

− 2.77

(− 5.83; 0.28)

*

Dual chamber P (vs. CRT-P/CRT-D)

− 1.84

(− 4.11; 0.43)

*

Single chamber ICD (vs. CRT-P/CRT-D)

− 3.49

(− 5.67; − 1.32)

*

Dual chamber ICD (vs. CRT-P/CRT-D)

0.06

(− 2.94; 3.06)

*

Device manufacturer

0.243

Boston Scientific (vs. Medtronic)

1.59

(− 0.62; 3.81)

*

Biotronik, LivaNova (Ela/Sorin), Vitatron (vs. Medtronic)

1.20

(− 1.18; 3.59)

*

St. Jude Medical (vs. Medtronic)

− 0.67

(− 2.48; 1.15)

*

  1. Linear regression was applied to adjust for intergroup differences in indicated parameters; * a single p value is provided for parameters “device type” and “device manufacturer”
  2. Italic value indicates statistically significant associations
  3. CRT cardiac resynchronization therapy device, D defibrillator, EP electrophysiology, ICD implantable cardioverter defibrillator, P pacemaker