# Effects of external diaphragm pacing combined with repetitive peripheral magnetic stimulation of the phrenic nerve on respiratory function in stroke patients

**Authors:** Qin Zhang, Chengshuo Wang, Hongfei Cai, Shasha Jin, Qian Wang, Yanxin Fu, Aomeng Xiang, Jingman Qi, Liang Wu, Bin Liu

PMC · DOI: 10.3389/fmed.2025.1596850 · Frontiers in Medicine · 2025-07-16

## TL;DR

This study finds that combining diaphragm pacing and magnetic nerve stimulation improves breathing function more than either treatment alone in stroke patients.

## Contribution

The novel finding is that combined external diaphragm pacing and repetitive peripheral magnetic stimulation yields greater respiratory improvements than monotherapies in stroke patients.

## Key findings

- Combined treatment group showed significantly greater improvements in FVC, FEV1, and MIP compared to monotherapy groups.
- Combined treatment led to more pronounced increases in diaphragmatic thickness and excursion than either EDP or rPMS alone.
- Combined treatment resulted in a more significant reduction in phrenic nerve conduction time compared to monotherapies.

## Abstract

To investigate the effects of external diaphragmatic pacing (EDP) and repetitive peripheral magnetic stimulation (rPMS) of the phrenic nerve on respiratory function in stroke patients.

Fifty-four stroke patients were randomly assigned to three groups: an EDP group (n = 18), an rPMS group (n = 18), and a combined treatment group (n = 18). All groups received routine breathing training. Additionally, the EDP group underwent EDP, the rPMS group received repeated peripheral magnetic stimulation of the phrenic nerve, and the combined treatment group received a combination of both interventions. The treatment regimen lasted for 4 weeks. Pulmonary function parameters, including forced vital capacity (FVC), forced expiratory volume in 1 s (FEV1), FEV1/FVC%, peak expiratory flow (PEF), maximal inspiratory pressure (MIP), and maximal expiratory pressure (MEP), were assessed using a pulmonary function tester. Diaphragmatic thickness (DT) and diaphragmatic excursion (DE) were evaluated via ultrasound imaging, whereas compound muscle action potential (CMAP) amplitude and phrenic nerve conduction time (PNCT) were measured using transcranial magnetic stimulation technology.

Following 4 weeks of treatment, significant improvements were observed in FVC, FEV1, PEF, MIP, and MEP across all three groups (all p < 0.05). Moreover, the combined treatment group demonstrated significantly greater improvements in FVC, FEV1, and MIP compared with either the EDP or rPMS group (p < 0.05). DT and DE were also significantly increased in all groups (p < 0.05), with more pronounced improvements in the combined treatment group than in the other groups (p < 0.05). In all three groups, CMAP amplitude increased significantly, whereas PNCT decreased significantly (p < 0.05). Furthermore, the reduction in PNCT was more obvious in the combined treatment group than in either the EDP or rPMS group (p < 0.05).

Compared with monotherapy using either EDP or rPMS, combined treatment demonstrates significantly greater efficacy in promoting respiratory function rehabilitation in stroke patients. Additionally, it shows potential advantages in improving phrenic nerve motor conduction.

## Linked entities

- **Diseases:** stroke (MONDO:0005098)

## Full-text entities

- **Diseases:** Respiratory conditions (MESH:D012131), pulmonary dysfunction (MESH:D011660), pulmonary and thoracic-abdominal disease (MESH:D000007), diaphragmatic atrophy (MESH:C536880), critical condition (MESH:D016638), impaired thoracic expansion (MESH:D013896), diaphragmatic fatigue (MESH:D005221), hemorrhage (MESH:D006470), lung cancer (MESH:D008175), DT (MESH:D006548), cognitive, emotional, or mental disorders (MESH:D003072), neck pain (MESH:D019547), atrophy (MESH:D001284), impairment of vital organ function (MESH:D019965), tuberculosis (MESH:D014376), musculoskeletal issues (MESH:D009140), PNCT (MESH:D000377), atelectasis (MESH:D001261), Pulmonary infection (MESH:D012141), allergies (MESH:D004342), pneumonia (MESH:D011014), diaphragmatic dysfunction (MESH:D056989), seizures (MESH:D012640), cough (MESH:D003371), Cerebrovascular Diseases (MESH:D002561), Pulmonary function decline (OMIM:608852), Stroke (MESH:D020521), rib fractures (MESH:D012253), Brain injuries (MESH:D001930), cerebral hemorrhage or infarction (MESH:D002544), cerebral and neural impairments (MESH:D002547), Brain stem infarction (MESH:D020526), CMAP (MESH:D009207), muscle wasting (MESH:D009133), respiratory muscle cell loss (MESH:D012133), skin damage (MESH:D012871), muscle fibrosis (MESH:D005355), Unilateral limb paralysis (MESH:C535349), Respiratory muscle weakness (MESH:D018908), COPD (MESH:D029424), hemiplegic (MESH:D020233)
- **Chemicals:** oxygen (MESH:D010100), AMT (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12307151/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12307151/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12307151/full.md

---
Source: https://tomesphere.com/paper/PMC12307151