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Table 3 Adverse event and serious adverse event counts, percentages given in brackets, for 132 patients, who underwent total knee arthroplasty (TKA) before implementation of a critical pathway on TKA, versus 128 patients, who underwent TKA after path implementation

From: Adverse events in total knee arthroplasty: Results of a physician independent survey in 260 patients

 

Before pathway implementation

After pathway implementation

Total

adverse event

n = 132

n = 128

n = 260

Generalised seizure due to local anaesthetic intoxication

0 (0)

1 (1)

1 (0)

DVT (lower leg)

10 (8)

6 (5)

16 (6)

DVT (knee)

4 (3)

2 (2)

6 (2)

DVT (thigh)

0 (0)

1 (1)

1 (0)

Haematoma

1 (1)

3 (2)

4 (2)

Wound healing problems

1 (1)

0 (0)

1 (0)

Stiff knee

0 (0)

1 (1)

1 (0)

Gastrointestinal bleeding

0 (0)

3 (2)

3 (1)

Dekubital ulcer

1 (1)

2 (2)

3 (1)

Postoperative cognitive disorder

1 (1)

0 (0)

1 (0)

Speech disturbance and Hyperkinesia in Parkinson disease

2 (2)

1 (1)

3 (1)

Postoperative hypertonia

1 (1)

3 (2)

4 (2)

Cardiac blocks

2 (2)

2 (2)

4 (2)

Diarrhoea

1 (1)

1 (1)

2 (1)

Obstipation

0 (0)

1 (1)

1 (0)

Erysipel

1 (1)

0 (0)

1 (0)

Exanthema

1 (1)

3 (2)

4 (2)

Otolaryngology consultation*

2 (2)

0 (0)

2 (1)

Dentist consultation*

1 (1)

0 (0)

1 (0)

Urinary tract infection

0 (0)

2 (2)

2 (1)

Urologic consultation*

1 (1)

2 (2)

3 (1)

Fall

0 (0)

2 (2)

2 (1)

Posterior collum lesion (myelon)*

0 (0)

1 (1)

1 (0)

Hyperhomocystinemia*

0 (0)

1 (1)

1 (0)

Total AE

30 (23)

38 (29)

68 (26)

serious adverse event

Death during study period, unrelated

1 (1)

1 (1)

2 (1)

Resuscitation (cardiological cause)

1 (1)

0 (0)

1 (0)

Pulmonary embolism

1 (1)

0 (0)

1 (0)

Revision for infection

1 (1)

3 (2)

4 (2)

Revision for haematoma

1 (1)

0 (0)

1 (0)

Closed mobilisation

0 (0)

3 (2)

3 (1)

Opticusneuropathia

0 (0)

1 (1)

1 (0)

Myocardial infarction

0 (0)

1 (1)

1 (0)

Central vein thrombosis eye

0 (0)

1 (1)

1 (0)

Subcutaneous infection belly (related to DVT prophylaxis)

0 (0)

1 (1)

1 (0)

Total SAE

5 (4)

11 (9)

16 (6)

  1. * Adverse events unrelated to surgical treatment