Skin perfusion pressure measured by isotope washout in legs with arterial occlusive disease: Evaluation of different tracers, comparison to segmental systolic pressure, angiography and transcutaneous oxygen tension and variations during changes in systemic blood pressure

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Abstract
Summary. The skin perfusion pressure (SPP) measured as the isotope washout cessation external pressure is valuable in selection of major amputation level. Five methodological investigations important to clinical use were carried out: (1) In five normal legs and 10 legs with arterial occlusive disease (AOD), 131I‐antipyrine (1311‐‐a.p.) was compared to Na(131I‐) and 99Tcm‐I pertechnetate (99Tcm). The average SPP by 131I‐a.p. and by 131I‐ were approximately equal, 57·0 mmHg (range 18–93) compared to 56·3 mmHg (range 13–88) (P > 0·1). The average SPP by 99Tcm was just slightly higher, 60·3 mmHg (range 18–98) (P < 0·02). The average washout constant for the three different tracers were approximately equal and correlated statistically significant with the SPP; (2) In 59 legs with AOD, segmental SPP was compared to segmental systolic blood pressures on the thigh, calf, ankle and first digit (strain gauge technique). The two different methods correlated statistically significant at all four levels, but the systolic blood pressures were higher than the SPP in particular in diabetic legs; (3) Angiograms in 35 legs with AOD showed that the SPP on the ankle was only consistently decreased in legs with arterial occlusions at two levels or more; (4) In 47 legs with AOD, the SPP on the calf or on the thigh was compared with transcutaneously measured PO2. The two different methods correlated statistically significant, but the scatter was great; (5) During induced variations in systemic blood pressure in seven patients (12 legs with AOD), the segmental SPP and the segmental systolic blood pressure were found on average to vary in proportion with the intra‐arterial mean and systolic pressure respectively; however, this proportional relationship was not valid for the individual leg. It is concluded that 99Tcmis as suitable as the 131I‐labelled tracers in estimating the SPP. The SPP is significantly correlated to skin blood flow, to systolic blood pressure, to tc PO2 and to angiographic findings. Correction of SPP for systemic blood pressure changes can be made in proportion with the measured variations in systemic mean blood pressure. but only for groups of patients.