How the insurance industry reviews new medical devices and technology for approval and reimbursement under indemnity and HMO contracts

William B. Spector
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引用次数: 1

Abstract

In the course of development of medical insurance as a product, the first policies were designed to address medical issues which, for all practical purposes, were simple in comparison to those today. In the 1940s and somewhat into the 1950s, technology did not have a tremendous impact on the cost of delivering health care. During the 1960s technology surged ahead, propelled by a great deal of grant monies, which continued to be readily obtainable into the 1970s. However, toward the middle-to-late portion of the 1970s and early 1980s this seemingly unlimited resource for funding came to an end. Insurance companies needed to change their methods of assessment of risk, and the medical profession was forced to change its methods of practicing medicine. These factors combined to contribute to the current climate, especially as it relates to the state of claims processing and reimbursement for health care technology. What the 1990s will bring, while not obvious, is still predictable based on history.<>
保险业如何审查新的医疗设备和技术,以便在赔偿和HMO合同下获得批准和报销
在医疗保险作为一种产品的发展过程中,最初的政策是为了解决医疗问题而设计的,与今天的医疗问题相比,这些政策实际上是简单的。在20世纪40年代和50年代,技术并没有对提供医疗保健的成本产生巨大影响。在20世纪60年代,在大量赠款的推动下,技术突飞猛进,这些赠款一直持续到20世纪70年代。然而,到了20世纪70年代中后期和80年代初,这种看似无限的资金来源戛然而止。保险公司需要改变其评估风险的方法,医疗行业被迫改变其行医方法。这些因素加在一起,造成了目前的状况,特别是在医疗保健技术索赔处理和报销状况方面。20世纪90年代将会发生什么,虽然不明显,但根据历史仍然是可以预测的。
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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