Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

< Back to Article

Fig 1.

Study cohort selection.

* Statutory health insurance company; † Control group with PIM alternatives as stated in the PRISCUS publication. Patients receiving solely “other” drugs were prescribed neither a PIM nor a PIM alternative.

More »

Fig 1 Expand

Fig 2.

Index date with preceding washout period and subsequent follow-up time.

PIM and PIM alternatives according to PRISCUS paper defined by ATC- and PZN-Code. ● End of individual follow-up after dispense date (maximum: 180 days).

More »

Fig 2 Expand

Table 1.

Baseline characteristics of older adults classified as cases (PIM group) or controls (PIM alternatives).

More »

Table 1 Expand

Table 2.

Comparison of the type of admission to a hospital in cases (PIM group) and controls (PIM alternatives).

More »

Table 2 Expand

Table 3.

Polypharmacy in cases (PIM group) and controls (PIM alternatives).

More »

Table 3 Expand

Fig 3.

Eight most common PIM drug classes.

More »

Fig 3 Expand

Table 4.

Incident hospitalizations during the 180-day follow-up period after the index date in cases (PIM group) and controls (PIM alternatives).

More »

Table 4 Expand

Table 5.

Hazard Ratios (HR) for hospitalization within 180 days after index date.

More »

Table 5 Expand

Fig 4.

Kaplan-Meier survival curves for hospitalization-free survival during the 180 days of follow-up.

Survival curves indicate an association between risk of all-cause hospitalization and use of PIMs.

More »

Fig 4 Expand