# Sex-specific short- and long-term outcomes in patients with leadless cardiac pacemakers

**Authors:** Daniel Kiblboeck, Karim Saleh, Jakob Boetscher, Hannah Rohringer, Julian Maier, Justin Lacher, Christian Reiter, Joerg Kellermair, Helga Wagner, Stefan Raidl, Thomas Lambert, Clemens Steinwender, Hermann Blessberger

PMC · DOI: 10.1007/s00392-026-02891-w · Clinical Research in Cardiology · 2026-03-17

## TL;DR

This study examines whether outcomes for leadless cardiac pacemakers differ between men and women, finding no major sex-specific disparities in complications or mortality.

## Contribution

The study provides new insights into sex-specific outcomes of leadless cardiac pacemaker implantation in a single-center observational setting.

## Key findings

- Procedure-related complications were more common in women during LCP implantation.
- No significant differences were found in in-hospital or all-cause mortality between sexes.
- Concomitant lead extraction was the only predictor for complications or death during the index stay.

## Abstract

Safety and efficacy have been well demonstrated for Micra™ leadless cardiac pacemakers (LCPs). However, the presence of sex-specific disparities remains unclear.

The aim of this single-centre observational study was to assess the sex-specific short- and long-term outcomes in patients undergoing LCP implantation.

In total, 378 LCPs were implanted in 127 women (33.6%) and 251 men (66.4%). The most frequent indications included atrial fibrillation with slow conduction (women: 31.5%, men: 44.6%), third-degree atrioventricular block (women: 31.5%, men: 33.5%) and sick sinus syndrome (women: 21.3%, men: 9.6%). Electrical performance parameters of LCPs were similar between sexes. Procedure-related complications during LCP implantation occurred more frequently in women (3.1%) compared to men (0.4%), though no difference was observed for all complications during the index stay (women: 3.9%, men: 1.6%, p = 0.18). In-hospital mortality was low for women (0.8%) and men (0.8%, p = 0.96). A multivariable logistic regression analysis adjusted for sex, age, diabetes, chronic kidney disease, coronary artery disease and transcatheter and surgical valve replacement revealed concomitant lead extraction (OR 9.153, p = 0.001) as the only predictor for complication or death during index stay. All-cause mortality was 30.7% in women (n = 39) and 27.5% in men (n = 69, p = 0.28) during a median follow-up of 41 months (IQR 22–65 months).

No sex-specific disparities were observed with respect to complications during index stay, in-hospital and all-cause mortality. Less frequent use of LCP therapy in women may relate to differing indications between sexes. Further prospective studies may help to develop sex-specific recommendations for LCP therapy.

## Linked entities

- **Diseases:** atrial fibrillation (MONDO:0004981), third-degree atrioventricular block (MONDO:0000468), sick sinus syndrome (MONDO:0001823), diabetes (MONDO:0005015), chronic kidney disease (MONDO:0005300), coronary artery disease (MONDO:0005010)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}
- **Diseases:** myocardial infarction (MESH:D009203), ICD (OMIM:252500), cerebrovascular disease (MESH:D002561), DM (MESH:D009223), Atrial fibrillation (MESH:D001281), stroke (MESH:D020521), hypovolemic shock (MESH:D012769), pericardial effusion (MESH:D010490), cardio-inhibition (MESH:C565433), peripheral artery disease (MESH:D058729), CKD (MESH:D012080), infection (MESH:D007239), AV block (MESH:D054537), lead (MESH:D007855), sick sinus syndrome (MESH:D012804), CRT-D (MESH:D014808), syncope (MESH:D013575), TIA (MESH:D002546), septic shock (MESH:D012772), pseudoaneurysm (MESH:D017541), LCPs (MESH:D006331), sinus arrest (MESH:D054138), ) diseases (MESH:D004194), SSS (MESH:C566690), LCP (MESH:D007873), retroperitoneal bleeding (MESH:D012186), Malignant diseases (MESH:D009369), renal dysfunction (MESH:D007674), renal (MESH:D006030), death (MESH:D003643), bradyarrhythmias (MESH:D001919), Left bundle branch block (MESH:D002037), hypertension (MESH:D006973), hematoma (MESH:D006406), Cardiovascular disease (MESH:D002318), neurological ( (MESH:D009461), and infectious (MESH:D003141), CIED infection (MESH:D009471), cardiogenic shock (MESH:D012770), underweight (MESH:D013851), endocarditis (MESH:D004696), Atrial fibrillation or flutter (MESH:D001282), pulmonary abscess (MESH:D008169), neurological diseases (MESH:D020271), chronic kidney disease (MESH:D051436), Valvular heart disease (MESH:D006349), frailty (MESH:D000073496), AV fistula (MESH:D005402), venous thromboembolism (MESH:D054556), diabetes (MESH:D003920), COPD (MESH:D029424), coronary artery disease (MESH:D003324), tricuspid valve dysfunction (MESH:D014264), LV dysfunction (MESH:D018487), arrhythmia (MESH:D001145)
- **Chemicals:** NOAC (MESH:C065145), LCP (-), MRA (MESH:C502936), aldosterone (MESH:D000450), ACE (MESH:C024789), vitamin K (MESH:D014812)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13013215/full.md

## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC13013215/full.md

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Source: https://tomesphere.com/paper/PMC13013215