| Literature DB >> 20619929 |
Abstract
The use of transmission precautions such as contact isolation in patients known to be colonised or infected with multidrug-resistant organisms is recommended in healthcare institutions. Although essential for infection control, contact isolation has recently been associated with adverse effects in patients. We undertook a systematic review to determine whether contact isolation leads to psychological or physical problems for patients. Studies were included if (1) hospitalised patients were placed under isolation precautions for an underlying medical indication, and (2) any adverse events related to the isolation were evaluated. We found 16 studies that reported data regarding the impact of isolation on patient mental well-being, patient satisfaction, patient safety or time spent by healthcare workers in direct patient care. The majority showed a negative impact on patient mental well-being and behaviour, including higher scores for depression, anxiety and anger among isolated patients. A few studies also found that healthcare workers spent less time with patients in isolation. Patient satisfaction was adversely affected by isolation if patients were kept uninformed of their healthcare. Patient safety was also negatively affected, leading to an eight-fold increase in adverse events related to supportive care failures. We found that contact isolation may negatively impact several dimensions of patient care. Well-validated tools are necessary to investigate these results further. Large studies examining a number of safety indicators to assess the adverse effects of isolation are needed. Patient education may be an important step to mitigate the adverse psychological effects of isolation and is recommended. Copyright 2010 The Hospital Infection Society. Published by Elsevier Ltd. All rights reserved.Entities:
Mesh:
Year: 2010 PMID: 20619929 PMCID: PMC7114657 DOI: 10.1016/j.jhin.2010.04.027
Source DB: PubMed Journal: J Hosp Infect ISSN: 0195-6701 Impact factor: 3.926
Figure 1Literature search process.
Study demographics
| Study | Study design | Controls | Target population | No. of patients ( | Setting | Reason for isolation | Type of isolation |
|---|---|---|---|---|---|---|---|
| Catalano | Case–control | Non-isolated patients with infection | Adults | 27/24 | Infectious disease ward | VRE, MRSA | C |
| Cohen | Case–control | Patients on standard precautions | Children | 24/41 | Medical ward | HAI | C, A, D |
| Evans | Case–control | Non-isolated matched controls in SICU/ward | Adults | 48/48 | Surgical ward/ICU | HAI | C, D |
| Gammon | Case–control | Non-isolated patients in the ward for at least 7 days | Adults | 20/20 | Medical ward | Mixed infection | C |
| Gasink | Case–control | Non-isolated patients in the ward for at least 3 days | Adults | 43/43 | Medical/surgical ward | Mixed infection | C |
| Kennedy and Hamilton | Prospective cohort | – | Adults | 16/16 | Medical ward | MRSA | C |
| Klein | Randomised controlled trial | Patients randomised to standard hospital care | Children | 32/38 | ICU | Infection, NS | C |
| Kirkland and Weinstein | Case–control | Non-isolated patients in the ICU | Adults | 29/88 | MICU | MDRO | C |
| Maunder | Retrospective cohort | – | Adults | 19 | ICU, medical ward | SARS | A, C |
| Newton | Prospective cohort | – | Adults | 19 | Medical ward | MRSA | C |
| Rees | Prospective cohort | – | Adults | 21 | Rehabilitation ward | Mixed infection | A, C |
| Saint | Prospective cohort | – | Adults | 31/108 | Medical ward | Infection, NS | C |
| Stelfox | Case–control with two matched cohorts: a general cohort plus a CHF cohort | Non-isolated patient who occupied the same bed, and was admitted immediately before, or after the patient in isolation | Adults | 78/156 (72/144) | Medical ward | MRSA | C |
| Tarzi | Prospective cohort | – | Adults | 22/20 | Rehabilitation ward | MRSA | C |
| Wilkins | Prospective cohort | – | Adults | 41 | Infectious disease ward | Infection, NS | C |
VRE, vancomycin-resistant enterococcus; MRSA, meticillin-resistant Staphylococcus aureus; HAI, hospital-acquired infection; SICU, surgical intensive care unit; SARS, severe acute respiratory syndrome; NS, not specified; C, contact; A, airborne; D, droplet; CHF, congestive heart failure.
Summary of study methodology and outcomes
| Study | Methodology | Psychometric tools | Main outcome | Time of assessment | Results |
|---|---|---|---|---|---|
| Catalano | Psychometric tools | Hamilton Depression Rating Scale (HAM-D), Hamilton Anxiety Rating Scale (HAM-A) | Psychological impact | At day 7 and day 14 | HAM-D and HAM-A scores were higher for cases than controls ( |
| Cohen | Direct observation by a single worker not part of the healthcare team during morning rounds. | Pediatric Family Satisfaction Questionnaire (PFSQ) | Time spent in direct patient care. | At 48 h | No difference in either direct patient care or quality of care |
| Evans | Direct observation by a healthcare worker. | 16 item questionnaire | Time spent in direct patient care | 2 h daily for 5 weeks | No. of encounters/h and contact time/h was higher for non-isolated than for isolated ( |
| Gammon | Multiple psychometric tools | Hospital Anxiety and Depression Scale (HADS), Health Illness Questionnaire (HIQ), Self-Esteem Scale (SES) | Psychological impact | At day 7 | Mean Anxiety and Depression scores higher in isolated patients ( |
| Gasink | Questionnaire | Consumer Assessment of Healthcare Providers and Systems (CAHPS) | Patient care satisfaction | At day 3 | No difference in patient care satisfaction |
| Kennedy and Hamilton | Multiple psychometric tools | Beck Depression Inventory (BDI), State Anxiety Inventory (STAI –Form), Profile of Mood States (POMS) | Psychological impact | In isolation for at least 2 weeks | Isolated patients with higher POMS Anger–Hostility scores |
| Klein | Direct observation by investigator | – | Incidence of nosocomial infection | For 1 h on days 1, 3 and 7 | Isolation reduced nosocomial infection rates. Patient care was not compromised, and isolation was well-tolerated |
| Kirkland and Weinstein | Direct observation (not specified by whom) | – | Frequency of patient encounters | 35 observation periods lasting 1 h each, over 7 months | Patients in isolation: fewer room entries/h ( |
| Maunder | Interview of patients with and without SARS by mental health professionals and consultation–liaison psychiatrists | – | Psychological impact | 4 weeks | Isolated patients reported fear, loneliness, anxiety, depression |
| Newton | Interview by infection control nurse | – | Psychological impact | During isolation | Mixed patient experiences during isolation |
| Rees | Psychometric tools | HADS | Psychological impact and patient satisfaction | During isolation | 12/21 had depression, based on HADS. Satisfaction was related to information/education |
| Saint | Direct observation by study investigator | – | Time spent in direct patient care | On several days/month for 6 months, during morning rounds | Attending physicians spent less time examining patients in isolation (RR = 0.49, |
| Stelfox | Medical chart review | – | Patient adverse events, described as injuries caused by medical management | During isolation | Cases had fewer vital sign recordings ( |
| Tarzi | Multiple psychometric tools | Abbreviated Mental Test Score (AMTS), Barthel Index (BI), Geriatric Depression Scale (GDS), POMS | Psychological impact | – | GDS scores were higher in isolated patients ( |
| Wilkins | Psychometric tools | Crown–Crisp Experiential Index (CCEI) | Psychological impact | On admission | Admission scores for hysteria, anxiety and total scores were increased for patients in isolation |