Observational retrospective study on the effectiveness of sequential graduated intermittent pneumatic compression therapy of lower limbs edema

E. Toma, Valentina Vanzi
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引用次数: 2

Abstract

The main aim of the study is to evaluate the effectiveness of sequential graduated intermittent pneumatic compression (SGIPC)therapy of lower limbs edema, regardless of its etiology. A retrospective observational study is conducted to determine the effectivenessof a regimen of sequential gradient SGIPC in treating edema of lower limbs. The study is carried out on 90 patients affected bydifferent stages of edema and evaluated at a Wound Care Clinic for one month. Medical records data have been collected after thefirst, the third, and the fifth hour-long treatment session. The inclusion criteria are: (1) presence of edema to one limb, at least,regardless of etiology, (2) presence of both pain and feeling of heaviness (or tiredness) of the limb, (3) non-use of bandages or elasticstocking/knee socks, and (4) availability of complete data about the edema size monitoring. The exclusion criteria are: (1) presenceof infected wounds, (2) severe arteriosclerosis or other ischemic vascular diseases, (3) severe congestive cardiac failure, (4) known orsuspected acute deep vein thrombosis (DVT), (5) thrombophlebitis or Pulmonary Embolism (PE), and (6) hypertension (SystolicPressure greater than 170mmHg). The following parameters are considered as grade of improvement: the decrease of the limbcircumference in at least two measurement points between the foot, ankle, and calf; the disappearance of at least one of thesymptoms of pain and feeling of heaviness of the limb; improved mobility. A Flowtron ACS 900 system is used, for the treatment,consisting of a pump, connected to two (calf and thigh) brace with individual tubes, applying a pneumatic compression, graduatedin the air chamber, with sequential cycle in three compartments (one at the calf level and two at the thigh level), at a pressure of45mmHg, with inflation cycles intermittent alternating. Inflation time 12s, time of deflation 48s. In addition, bracescorresponding to limb size have been used (automatically recognized by the system).In a sample of 90 patients (95.6% women and 4.4% men) with edema of the lower limbs (37.8% at stage 1, 43.3% at stage 2,15.6% at stage 3, and 3.3% at stage 4), a successful treatment has been found, from the first session. A circumference decreasegreater than 3mm in at least two measuring points between the foot, ankle, and calf, of 77.8% after the first session, 90% after thethird session, 90% after the fifth session, on average for both limbs. The disappearance of pain at the end of the session has beenfound in 85.6% of cases after the first session and 100% after the third and fifth, respectively. The feeling of heaviness of the limbhas disappeared in 100% of cases at the end of the sessions. For the stages 3 and 4, it is generally observed an improvement ofmobility in 58.9% of cases at the end of the first session and equal to 100% after the third and fifth session. A good compliance inpatients who have rejected the manual lymph drainage has been found. Moreover, a good applicability has been found in patientswith critical issues such as dermatoporosis and capillary fragility, and bariatric patients. In general, the patients haveunderestimated the edema, specifically only 21% of patients at a stage greater or equal to 2 have recognized the edema as a clinicalproblem.
顺序渐进式间歇气压治疗下肢水肿疗效的回顾性观察研究
该研究的主要目的是评估顺序渐进式间歇气动压缩(SGIPC)治疗下肢水肿的有效性,而不考虑其病因。一项回顾性观察研究旨在确定顺序梯度SGIPC治疗下肢水肿的有效性。该研究对90名不同阶段水肿患者进行了研究,并在伤口护理诊所进行了一个月的评估。在第一次、第三次和第五次治疗后收集了医疗记录数据。纳入标准是:(1)至少有一侧肢体出现水肿,无论病因如何;(2)肢体同时出现疼痛和沉重感(或疲倦感);(3)未使用绷带或弹力袜/短袜;(4)有水肿大小监测的完整数据。排除标准是:(1)存在感染伤口,(2)严重动脉硬化或其他缺血性血管疾病,(3)严重充血性心力衰竭,(4)已知或疑似急性深静脉血栓形成(DVT),(5)血栓性静脉炎或肺栓塞(PE),(6)高血压(收缩压大于170mmHg)。以下参数被认为是改善的等级:足、踝和小腿之间至少两个测量点的下肢围度减少;至少一种疼痛症状和肢体重重感消失;改善流动性。在处理过程中,使用了Flowtron ACS 900系统,该系统由一个泵组成,连接到两个(小腿和大腿)支架和单独的管道,在气室中进行气动压缩,在三个隔间(一个在小腿水平,两个在大腿水平)中进行顺序循环,压力为45mmhg,间歇交替进行充气循环。通货膨胀时间12秒,通货紧缩时间48秒。此外,还使用了与肢体尺寸相对应的支架(系统自动识别)。在90例下肢水肿患者(95.6%为女性,4.4%为男性)的样本中(第1期37.8%,第2期43.3%,第3期15.6%,第4期3.3%),从第一次治疗开始就发现了成功的治疗方法。在脚、脚踝和小腿之间至少两个测量点的周长减小大于3mm,在第一次训练后为77.8%,在第三次训练后为90%,在第五次训练后为90%。第一次疗程结束后,85.6%的患者疼痛消失,第三次和第五次疗程结束后,疼痛消失率分别为100%。在治疗结束时,四肢的沉重感100%消失了。对于第三和第四阶段,通常观察到58.9%的病例在第一次治疗结束时活动能力有所改善,在第三和第五次治疗后达到100%。对手工淋巴引流有排斥反应的住院患者依从性良好。此外,在皮肤疏松症、毛细血管脆性等重症患者和肥胖患者中也有很好的适用性。一般来说,患者低估了水肿,特别是在大于或等于2期的患者中,只有21%的患者认识到水肿是一个临床问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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