Hospital result
and target area
Quality objective
achieved?
All information
This is how often the decision to insert an artificial hip joint for the first time was made in accordance with the scientific guidelines
Hospital: 100,00 %
Target area: at least 90,00 %
Quality objective achieved
This is how often the decision to replace an artificial hip joint (or parts of it) was made in accordance with the scientific guidelines
Hospital: Data protection
No information due to data protection
Target area: at least 86,00 %
Quality objective achieved
Why?
This is haow rarely the waiting time for the insertion of an artificial hip joint after a femoral neck fracture was longer than recommended
Hospital: 6,35 %
Target area: at most 15,00 %
Quality objective achieved
This is how often preventive measures were trained with patients after surgery to avoid another fall
Hospital: 100,00 %
Target area: at least 90,00 %
Quality objective achieved
Ratio of actual to expected number of patients with general complications who had an artificial hip joint implanted after a femoral neck fracture
Hospital: 1,17
Target area: at most 2,25
Quality objective achieved
This is how rarely general complications (blood clots, pneumonia, cardiovascular problems) occurred during the planned first-time insertion of an artificial hip joint
Hospital: Data protection
No information due to data protection
Target area: at most 5,77 %
Quality objective achieved
This is how rarely general complications (blood clots, pneumonia, cardiovascular problems) occurred during operations in which an old artificial hip joint is replaced by a new one (replacement operation)
Hospital: Data protection
No information due to data protection
Target area: at most 20,00 %
Quality objective achieved
This ist how rarely specific complications occured (wound infections, bleeding, re-fractures) due to the use of an artificial hip joint after a femoral neck fracture
Hospital: 7,94 %
Target area: at most 11,63 %
Quality objective achieved
This is how rarely specific complications occured (wound infections, bleeding, new fractures) due to the initial insertion of an artificial hip joint
Hospital: 0,00 %
Target area: at most 8,01 %
Quality objective achieved
Ratio of actual to expected number of patients who experienced specific complications when replacing an old artificial hip joint with a new one (or when replacing individual components)
Hospital: 0,00
Target area: at most 2,02
Quality objective achieved
Ratio of actual to expected number of patients who experienced problems with the implant (misalignment, displacement, material fracture, etc.) when replacing an old artificial hip joint with a new one.
Hospital: 0,00
as rarely as possible
Evaluation is not available
Ratio of actual to expected number of patients who experienced wound infections, vascular injuries, nerve damage, post-operative bleeding and other soft tissue complications when replacing an old artificial hip joint with a new one.
Hospital: 0,00
as rarely as possible
Evaluation is not available
Ratio of the actual number to the previously expected number of patients who could not walk 50 metres when discharged from hospital (individual risks of the patients were taken into account)
Hospital: 0,54
Target area: at most 2,42
Quality objective achieved
This is how rarely patients died during their hospital stay after having an artificial hip joint implanted
Hospital: 0,00 %
Sentinel Event
Quality objective achieved
Ratio of actual to expected number of patients who received an artificial hip joint after a fracture of the neck of the femur and died during the operation.
Hospital: 0,25
as rarely as possible
Evaluation is not available
Ratio of the actual number to the previously expected number of patients in whom the artificial hip joint or individual parts were replaced (based on the period of 90 days after the operation in which the artificial hip joint was first inserted - individual risks of the patients were taken into account)
Hospital: 0,70
Target area: at most 2,27
Quality objective achieved