# Effect of Dystocia Duration on the Placental Health in Canines

**Authors:** Romina Gisele Praderio, Mauricio Javier Giuliodori, Rodolfo Luzbel de la Sota, María Alejandra Stornelli

PMC · DOI: 10.3390/life16020349 · 2026-02-18

## TL;DR

This study shows that longer dystocia in dogs is linked to worse placental health, suggesting early intervention can improve puppy survival.

## Contribution

The study introduces the placenta as a potential biomarker for fetal distress during canine dystocia.

## Key findings

- Longer dystocia duration correlates with increased placental necrosis and mineralization.
- Severe placental lesions are associated with higher risk of poor neonatal survival.
- Early obstetric intervention is recommended to reduce fetal hypoxia and improve outcomes.

## Abstract

The study aimed to determine whether placental lesions differ according to the duration of dystocia. Forty-seven placentas were obtained from 18 bitches that underwent emergency cesarean sections. For descriptive purposes, the cases were classified into four groups based on the duration of dystocia: Group A, up to 6 h; Group B, 6–11.9 h; Group C, 12–24 h; and Group D, more than 24 h. Forty-seven placentas were studied. Both macroscopic and microscopic characteristics were evaluated in each placenta. Descriptive data were presented, and logistic and multinomial regression models were used to assess whether dystocia duration (in hours) is associated with the presence and severity of placental macro- and microscopic lesions. An hour increment over the mean in the duration of dystocia showed a non-significant trend to increasing the presence of macroscopic necrosis (OR: 1.11, p = 0.09) and mineralization (OR: 1.10, p = 0.06), and it also increased the severity of macroscopic congestion (OR: 1.44; p = 0.01) and showed a non-significant trend to increasing the severity of polymorphonuclear neutrophil infiltrate (OR: 1.18; p = 0.06). These findings highlight the importance of early obstetric intervention in all cases of dystocia to minimize fetal hypoxia and improve neonatal outcomes. Moreover, the placenta could serve as a biomarker for fetal distress, as the presence of severe lesions indicates an increased risk for reduced neonatal survival.

## Linked entities

- **Diseases:** dystocia (MONDO:0006737)
- **Species:** Canis lupus familiaris (taxon 9615)

## Full-text entities

- **Genes:** IGF1 (insulin like growth factor 1) [NCBI Gene 610255] {aka IGF-I, IGFI, IGFIA}, IL6 (interleukin 6) [NCBI Gene 403985] {aka IL-6}, TNF (tumor necrosis factor) [NCBI Gene 403922] {aka TNFA, TNLG1F, cTNF}, IGF2 (insulin like growth factor 2) [NCBI Gene 483664]
- **Diseases:** acidosis (MESH:D000138), placental damage (MESH:D010922), chorionic (MESH:C564876), congestion (MESH:D002311), intellectual disability (MESH:D008607), death (MESH:D003643), neurological impairment (MESH:D009422), disabilities (MESH:D009069), necrosis (MESH:D009336), fetal death (MESH:D005313), fetal distress (MESH:D005316), stillbirth (MESH:D050497), speech impairment (MESH:D013064), underweight (MESH:D013851), labor (MESH:D048949), preeclampsia (MESH:D011225), Dystocia (MESH:D004420), uterine rupture (MESH:D014597), visual impairment (MESH:D014786), injury to (MESH:D014947), inflammation (MESH:D007249), nutritional impairment (MESH:D009748), hypoxia (MESH:D000860), fetal hypoxia (MESH:D005311), hearing impairment (MESH:D034381), endometritis (MESH:D004716), convulsions (MESH:D012640), fetal depression (MESH:D005315), lesion (MESH:D009059), hemorrhages (MESH:D006470), obese (MESH:D009765), respiratory impairment (MESH:D012131)
- **Chemicals:** hematoxylin (MESH:D006416), H&amp;E (MESH:D006371), calcium salt (-), formalin (MESH:D005557), eosin (MESH:D004801), oxygen (MESH:D010100), paraffin (MESH:D010232)
- **Species:** Homo sapiens (human, species) [taxon 9606], Canis lupus familiaris (dog, subspecies) [taxon 9615]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941726/full.md

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Source: https://tomesphere.com/paper/PMC12941726