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针对心血管疾病患者性问题的性咨询。

Sexual counselling for sexual problems in patients with cardiovascular disease.

作者信息

Byrne Molly, Doherty Sally, Fridlund Bengt G A, Mårtensson Jan, Steinke Elaine E, Jaarsma Tiny, Devane Declan

机构信息

School of Psychology, National University of Ireland, Galway, St. Anthony's, Galway, County Galway, Ireland.

出版信息

Cochrane Database Syst Rev. 2016 Feb 24;2(2):CD010988. doi: 10.1002/14651858.CD010988.pub2.

DOI:10.1002/14651858.CD010988.pub2
PMID:26905928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6464754/
Abstract

BACKGROUND

Sexual problems are common among people with cardiovascular disease. Although clinical guidelines recommend sexual counselling for patients and their partners, there is little evidence on its effectiveness.

OBJECTIVES

To evaluate the effectiveness of sexual counselling interventions (in comparison to usual care) on sexuality-related outcomes in patients with cardiovascular disease and their partners.

SEARCH METHODS

We searched CENTRAL, MEDLINE, EMBASE, and three other databases up to 2 March 2015 and two trials registers up to 3 February 2016.

SELECTION CRITERIA

Randomised controlled trials (RCTs) and quasi-RCTs, including individual and cluster RCTs. We included studies that compared any intervention to counsel adult cardiac patients about sexual problems with usual care.

DATA COLLECTION AND ANALYSIS

We used standard methodological procedures expected by Cochrane.

MAIN RESULTS

We included three trials with 381 participants. We were unable to pool the data from the included studies due to the differences in interventions used; therefore we synthesised the trial findings narratively.Two trials were conducted in the USA and one was undertaken in Israel. All trials included participants who were admitted to hospital with myocardial infarction (MI), and one trial also included participants who had undergone coronary artery bypass grafting. All trials followed up participants for a minimum of three months post-intervention; the longest follow-up timepoint was five months.One trial (N = 92) tested an intensive (total five hours) psychotherapeutic sexual counselling intervention delivered by a sexual therapist. One trial (N = 115) used a 15-minute educational video plus written material on resuming sexual activity following a MI. One trial (N = 174) tested the addition of a component that focused on resumption of sexual activity following a MI within a hospital cardiac rehabilitation programme.The quality of the evidence for all outcomes was very low.None of the included studies reported any outcomes from partners.Two trials reported sexual function. One trial compared intervention and control groups on 12 separate sexual function subscales and used a repeated measures analysis of variance (ANOVA) test. They reported statistically significant differences in favour of the intervention. One trial compared intervention and control groups using a repeated measures analysis of covariance (ANCOVA), and concluded: "There were no significant differences between the two groups [for sexual function] at any of the time points".Two trials reported sexual satisfaction. In one trial, the authors compared sexual satisfaction between intervention and control and used a repeated measured ANOVA; they reported "differences were reported in favour of the intervention". One trial compared intervention and control with a repeated measures ANCOVA and reported: "There were no significant differences between the two groups [for sexual satisfaction] at any of the timepoints".All three included trials reported the number of patients returning to sexual activity following MI. One trial found some evidence of an effect of sexual counselling on reported rate of return to sexual activity (yes/no) at four months after completion of the intervention (relative risk (RR) 1.71, 95% confidence interval (CI) 1.26 to 2.32; one trial, 92 participants, very low quality of evidence). Two trials found no evidence of an effect of sexual counselling on rate of return to sexual activity at 12 week (RR 1.01, 95% CI 0.94 to 1.09; one trial, 127 participants, very low quality of evidence) and three month follow-up (RR 0.98, 95% CI 0.88 to 1.10; one trial, 115 participants, very low quality of evidence).Two trials reported psychological well-being. In one trial, no scores were reported, but the trial authors stated: "No treatment effects were observed on state anxiety as measured in three points in time". In the other trial no scores were reported but, based on results of a repeated measures ANCOVA to compare intervention and control groups, the trial authors stated: "The experimental group had significantly greater anxiety at one month post MI". They also reported: "There were no significant differences between the two groups [for anxiety] at any other time points".One trial reporting relationship satisfaction and one trial reporting quality of life found no differences between intervention and control.No trial reported on satisfaction in how sexual issues were addressed in cardiac rehabilitation services.

AUTHORS' CONCLUSIONS: We found no high quality evidence to support the effectiveness of sexual counselling for sexual problems in patients with cardiovascular disease. There is a clear need for robust, methodologically rigorous, adequately powered RCTs to test the effectiveness of sexual counselling interventions for people with cardiovascular disease and their partners.

摘要

背景

性问题在心血管疾病患者中很常见。尽管临床指南建议为患者及其伴侣提供性咨询,但关于其有效性的证据很少。

目的

评估性咨询干预措施(与常规护理相比)对心血管疾病患者及其伴侣与性相关结局的有效性。

检索方法

我们检索了截至2015年3月2日的Cochrane系统评价数据库(CENTRAL)、医学期刊数据库(MEDLINE)、荷兰医学文摘数据库(EMBASE)以及其他三个数据库,以及截至2016年2月3日的两个试验注册库。

入选标准

随机对照试验(RCT)和半随机对照试验,包括个体和整群RCT。我们纳入了将任何干预措施与为成年心脏病患者提供性问题咨询的常规护理进行比较的研究。

数据收集与分析

我们采用了Cochrane期望的标准方法程序。

主要结果

我们纳入了三项试验,共381名参与者。由于所采用的干预措施存在差异,我们无法合并纳入研究的数据;因此,我们对试验结果进行了叙述性综合分析。两项试验在美国进行,一项试验在以色列进行。所有试验均纳入了因心肌梗死(MI)入院的参与者,一项试验还纳入了接受冠状动脉旁路移植术的参与者。所有试验在干预后至少对参与者进行了三个月的随访;最长随访时间点为五个月。一项试验(N = 92)测试了由性治疗师提供的强化(共五小时)心理治疗性咨询干预措施。一项试验(N = 115)使用了一个15分钟的教育视频以及关于心肌梗死后恢复性活动的书面材料。一项试验(N = 174)测试了在医院心脏康复计划中增加一个关注心肌梗死后恢复性活动的组成部分。所有结局的证据质量都非常低。

纳入的研究均未报告来自伴侣的任何结局。两项试验报告了性功能。一项试验在12个不同的性功能子量表上比较了干预组和对照组,并使用重复测量方差分析(ANOVA)检验。他们报告干预组有统计学上的显著差异。一项试验使用重复测量协方差分析(ANCOVA)比较干预组和对照组,并得出结论:“在任何时间点,两组[性功能]之间均无显著差异”。

两项试验报告了性满意度。在一项试验中,作者比较了干预组和对照组的性满意度,并使用重复测量ANOVA;他们报告“报告的差异有利于干预组”。一项试验使用重复测量ANCOVA比较干预组和对照组,并报告:“在任何时间点,两组[性满意度]之间均无显著差异”。

所有三项纳入试验均报告了心肌梗死后恢复性活动的患者数量。一项试验发现有一些证据表明性咨询对干预完成后四个月报告的恢复性活动率(是/否)有影响(相对风险(RR)1.71,95%置信区间(CI)1.26至2.32;一项试验,92名参与者,证据质量非常低)。两项试验未发现性咨询对12周(RR 1.01,95% CI 0.94至1.09;一项试验,127名参与者,证据质量非常低)和三个月随访时恢复性活动率有影响的证据(RR 0.98,95% CI 0.88至1.10;一项试验,115名参与者,证据质量非常低)。

两项试验报告了心理健康状况。在一项试验中,未报告得分,但试验作者指出:“在三个时间点测量的状态焦虑方面未观察到治疗效果”。在另一项试验中,未报告得分,但根据比较干预组和对照组的重复测量ANCOVA结果,试验作者指出:“实验组在心肌梗死后一个月时焦虑显著更高”。他们还报告:“在任何其他时间点,两组[焦虑]之间均无显著差异”。

一项报告关系满意度的试验和一项报告生活质量的试验发现干预组和对照组之间没有差异。没有试验报告对心脏康复服务中性问题处理方式的满意度。

作者结论

我们没有发现高质量证据支持性咨询对心血管疾病患者性问题的有效性。显然需要进行有力的、方法严谨且样本量充足的随机对照试验,以测试性咨询干预措施对心血管疾病患者及其伴侣的有效性。

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