Abstract
As one of the efforts to prevent intimate partner violence (IPV) and intimate partner homicide, countries have adopted legislation requiring professionals to report cases of IPV, or suspected IPV injuries, to the police or the criminal justice system. The term for this is mandatory reporting. In spite of its good intention, mandatory reporting of IPV is a controversial issue. The objective of this review was to systematically search for, appraise the quality of, and synthetize the evidence from quantitative and qualitative studies on mandatory reporting of IPV. A systematic review of the scientific literature was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis guidelines. A comprehensive search was conducted through Ovid MEDLINE, PsycINFO, Scopus, Criminal Justice Abstracts, and SveMed+. Articles were included if they (a) were peer-reviewed empirical studies rather than theories or discussions, (b) described mandatory reporting of IPV, and (c) were written in English or Scandinavian languages. No time limit was applied. Twenty-five research studies met the criteria for review. Victims were generally supportive of a law requiring professionals to report IPV, although subsamples’ attitudes opposing mandatory reporting were presented as main findings in a substantial number of studies. Group differences between abused or nonabused women and knowledge about mandatory reporting of IPV among professionals was mixed and inconclusive. Few professionals had actually reported IPV under mandatory reporting. Empirical research appears to be scarce, with moderate to high degree of bias and with only limited recent development.
Keywords
As one of the efforts to protect individuals perceived to be at risk of harm, countries in different parts of the world have adopted legislation requiring professionals to report cases of IPV, or suspected IPV injuries, to the police or the criminal justice system. The most commonly used term for this is mandatory reporting (Jordan & Pritchard, 2018; A. Smith, 2000; World Health Organization [WHO], 2013). The purpose of mandatory reporting is to protect IPV victims from risk of harm, to relieve victims of having to report abusive partners themselves, and to improve the involvement of law enforcement and criminal justice response (Jordan & Pritchard, 2018; Rodriguez, Sheldon, & Rao, 2002). Furthermore, mandatory reporting sends a signal to abusive partners that IPV is a serious crime (A. Smith, 2000; WHO, 2013), and it establishes third-party documentation that may be critical to a criminal or civil legal action (Antle, Barbee, Yankeelov, & Bledsoe, 2010). Despite the legislation’s intention to protect, mandatory reporting of intimate partner violence (IPV) is a controversial issue. Supporters of the laws argue that mandatory reporting may increase victims’ safety by requiring professionals to report potential threats and thereby reduce the danger to victims (e.g., Antle et al., 2010). Critics argue that reporting requirements undermine victims’ autonomy and decision-making and may decrease willingness to disclose abuse and seek treatment for IPV injuries (e.g., Rodriguez et al., 2002). The authors conducted a review of the literature regarding this controversial issue to scrutinize the empirical evidence on mandatory reporting of IPV in the research literature.
Rationale
IPV comprises physical and sexual violence, stalking, and psychological aggression (including coercive tactics) by a current of former intimate partner (Breiding, Basile, Smith, Black, & Mahendra, 2015). An intimate partner is a person with whom one has a close personal relationship characterized by emotional connectedness, regular contact, ongoing physical and/or sexual contact, identity as a couple, and familiarity with each other’s lives (Breiding et al., 2015). The Centers for Disease Control and Prevention (2018) stresses that IPV is a “serious, preventable public health problem that affects millions of Americans.” Worldwide, almost one third of women who have been in a relationship have experienced physical and/or sexual violence by their intimate partner (WHO, 2013). A systematic review of the global prevalence of intimate partner homicide, which obtained data from 169 countries, found that 13.5% of all homicides were committed by an intimate partner, and this proportion was 6 times higher for female homicides than for male homicides (Stöckl et al., 2013). Interpretations of these findings conclude that at least one in the seven homicides globally and more than a third of female homicides are perpetrated by an intimate partner. In addition, such violence commonly represents the culmination of a long history of IPV (Stöckl et al., 2013). Strategies to reduce intimate partner homicide risk include increased IPV prevention, structured professional risk assessments, awareness, and support for victims and perpetrators of IPV (Stöckl et al., 2013; Vatnar, Friestad, & Bjørkly, 2017).
Mandatory Reporting of IPV Controversy
The WHO (2013) concluded that mandatory reporting of IPV by health-care providers is not recommended. WHO maintains that the practice is not supported by evidence and claims that mandatory reporting would “impinge on women’s autonomy and decision-making” as it, particularly, “does not appear to be the preference for abused women.” Additional arguments opposing the laws include concerns that mandatory reporting may undermine the doctor–patient relationship and lead to retaliation by the abuser (Antle et al., 2010). Despite their recommendation against mandatory reporting of IPV by health-care providers, WHO characterizes the quality of evidence concerning this practice as very poor, thus indicating a need for further research.
Despite the claimed importance of mandatory reporting, on the one hand, and the controversies surrounding the practice, on the other, there are, to our knowledge, currently no systematic reviews of IPV victims’ and perpetrators’ attitudes toward mandatory reporting nor on medical personnel’s attitudes, knowledge, and compliance with the reporting requirements. As far as we know, the evidence for supporting or opposing mandatory reporting of IPV is mixed and inconclusive.
Objectives
The objective of this review was to systematically search for, appraise the quality of, and synthetize the evidence for empirical studies on mandatory reporting of IPV. The research questions were the following: What is the extent of research on mandatory reporting of IPV? What has existing research found concerning mandatory reporting of IPV? We investigated this question from the perspectives of both (a) IPV victims and (b) professionals. What has existing research found concerning specific factors that support or oppose mandatory reporting of IPV?
Method
Protocol
A systematic review of the scientific literature was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis guidelines (PRISMA) (Moher, Liberati, Tetzlaff, & Altman, 2009). The review protocol consists of background information, review questions, inclusion and exclusion criteria, electronic search strategy, identification of research evidence, study selection, data extraction, quality assessment, data synthesis, and dissemination. The procedure is described below. A more detailed description of the protocol can be obtained from the first author.
Eligibility Criteria
Inclusion criteria for study type
Articles were included if they (a) were peer-reviewed empirical studies (quantitative and qualitative) rather than theories or discussions, (b) described mandatory reporting of IPV, and (c) were written in English or Scandinavian languages. No time limit was applied. Studies were excluded if they described mandatory reporting of child abuse, elder abuse, other misdeeds, or reported IPV that is regulated by organizational rules or routines and not by state or national law enforcement.
Inclusion criteria for mandatory reporting
Studies were included if they presented separate analyses of mandatory reporting of IPV and were either (1) systematic reviews of empirical studies on this specific topic or (2) papers reporting individual studies that met the inclusion criteria.
Search
A comprehensive search was conducted through multiple databases including Ovid MEDLINE, PsycINFO, Scopus, Criminal Justice Abstracts, and SveMed+. Full electronic search strategy used for the database Ovid MEDLINE: Epub Ahead of Print, In-Process & Other Non-Indexed Citations, Ovid MEDLINE(R) Daily, and Ovid MEDLINE(R) 1946 to Present. (1) Intimate Partner Violence/ or Domestic Violence/ or Spouse Abuse/ or Elder Abuse/ or Battered Women/ (2) ((partner* or domestic or spous* or woman or women or elder* or husband* or wife or wives or (significant and other*) or dating or relationship*) and (violen* or abus* or batter* or victim* or assault*)).ti. (3) (domestic violence or domestic abuse or spouse abuse or partner abuse or partner violence).ab. (4) (ipv or ipsa).ti, ab. (5) 1 or 2 or 3 or 4. (6) Mandatory Reporting/ (7) (reporting or reporter*).ti. (8) ((report or reports or reported or warn* or notif*) and (mandat* or duty or duties or designat* or oblig* or requir* or compulsory)).ti. (9) (mandat* and interven*).ti. (10) (mandatory report* or mandated report* or mandatory interven* or mandated interven*).ab. (11) (“duty to report” or “duties to report” or “duty to warn” or “duties to warn”).ab. (12) 6 or 7 or 8 or 9 or 10 or 11. (13) 5 and 12 (14) remove duplicates from 13. (15) limit 14 to (danish or english or norwegian or swedish). The full electronic search strategy used for the other databases can be obtained by request to the first author.
Information Sources
We conducted a systematic computer search on May 9, 2018, and an identical update search on January 11, 2019. The databases and resulting number of publications were as follows: Ovid MEDLINE, 647 publications; PsycINFO, 283; Scopus, 74; Criminal Justice Abstracts, 16; and SveMed+, 5. The total was 1,025 publications. After removal of duplicates, 860 original publications remained. After the study selection process, we conducted a hand search through the reference lists of the eligible articles for additional relevant articles.
Study Selection
References were recorded and managed in EndNote Version 8 (software). All studies were screened by title and abstract and key words (by the first author). If this step did not provide clear information that answered the eligibility questions, the full text was obtained. Both first and second author assessed full-text independent coding according to the following items: authors, year published, description of empirical study, discussion of mandatory reporting of IPV, inclusion of separate analyses for mandatory reporting of IPV, and whether it was a review study. Articles that were considered by consensus to meet the criteria were included in the review study.
Data Collection Process and Data Items
Each study was registered chronologically by a systematic assessment of the following items: authors, year, aim of the study, sample, methods, statistical analyses, and results. All results pertaining to mandatory reporting of IPV were registered. Based on a preliminary review, the categories used for registration were (1) female patients’ perspectives, (1a) IPV abused versus nonabused, (1b) supporting versus opposing mandatory reporting, (2) professionals’ perspectives (e.g., health-care providers, law enforcement providers, emergency departments, dental professionals, physicians, paramedics, clinicians), (2a) awareness, (2b) attitudes, (2c) and behavior.
Risk of Bias in Individual Studies
Each study was evaluated regarding design, strength of statistical analyses, degree distinctness of definitions, validity and reliability of measurements, number of participants, and sample characteristics. Bias and study limitations for quantitative studies were assessed at the outcome level by Hoy et al. (2012) Online Appendix 1: Risk of Bias Tool. Bias and Study Limitations for Qualitative Studies were monitored at the outcome level by using Tong, Sainsbury, and Craig (2007), Online Appendix 2: Consolidated Criteria for Reporting Qualitative (COREQ) studies.
Summary Measures
The quantitative studies were investigated, by two independent raters, for information on prevalence and for results from bivariate and multivariate variance analyses for group differences and associations between variables (linear and logistic regression). All findings with p ≤ .05 were registered as significant. The qualitative papers were examined by two independent raters for information about the analytical strategies, derivation of main themes, and the conclusions (Tong, Sainsbury, & Craig, 2007).
Synthesis of Results
All findings pertaining to mandatory reporting of IPV were classified as significant or insignificant associations. The results were separated in the discussion according to study type: studies of victims’ or patients’ attitudes to mandatory reporting of IPV and studies of professionals’ awareness, attitudes, and behaviors concerning mandatory reporting.
Risk of Bias Across Studies
We considered publication bias and whether some countries were disproportionately represented. We also looked for cultural context and location bias across the studies. Choice of study type, measurement, level of analyses, population, economic compensation, and group sizes were other possible risks of bias across studies. In small samples, the risk of statistical Type II errors increases. In such cases, we explored whether this risk was addressed and integrated into the interpretations and presentations of the actual findings.
Study Selection
The process of the selection of studies is presented in flow diagram (Figure 1). Among the 860 articles retrieved by the search, 15 were digitally listed with the term review in the title or key words. We excluded all 15 of these articles, either because they were not systematic reviews or did not meet other inclusion criteria. As there were no eligible systematic reviews, we proceeded to Step 2, original studies. Following the first author’s initial screening, 44 full-text articles were assessed by the first and second author independently. Of these 44 studies, 40 reported findings from original studies, and 4 were discussions of issues and cases with no empirical measurements provided. These were excluded. Among the remaining 40 papers, there were 37 that focused on mandatory reporting of domestic violence. Only 25 of these 37 included analyses that distinguished mandatory reporting for IPV, and these 25 were included in the present study (Table 1). The reference lists of the 25 articles were hand searched for additional relevant articles. None of the 11 full-text publications found by hand searches met the inclusion criteria.

Flow diagram.
Summary of Reviewed Studies.
Note. IPV = intimate partner violence. ED = emergency department.
a We found errors in the calculation and/or reporting of the numerator and/or denominator in the original studies (Hoy et al., 2012).
In summary, Step 1 yielded no systematic reviews. Step 2 yielded 25 original empirical studies. A hand search resulted in 0 additional original studies. A total of 25 publications were thus included in the present study.
Results
Study Characteristics
The 25 studies were published between 1994 and 2018 (see Table 1). A majority of them (n = 23) used quantitative analyses or quantifications. Two studies used qualitative analyses. A total of 35 analysis units (range = 1–3 units of analysis per study) were found. One study used qualitative analysis of single-person interviews (Antle et al., 2010) and the other one focus group interviews (Rodriguez, Craig, Mooney, & Bauer, 1998). All except two studies, which came from Korea (Cho, Cha, & Yoo, 2015) and Australia (Sawyer, Parekh, Williams, & Williams, 2014), were conducted in the United States. Nine studies (36%) claimed they had conducted multivariate analyses (logistic regression analyses; Table 1). Still, only seven studies reported results from logistic regression analyses (Gielen et al., 2000; Jordan & Pritchard, 2018; Rodriguez, McLoughlin, Bauer, Paredes, & Grumback, 1999; Rodriguez, McLoughlin, Nah, & Campbell, 2001; Rodriguez et al., 2002; Sachs, Koziol-McLain, Glass, Webster, & Campbell, 2002; A. Smith & Parsons Winokur, 2004; Table 2). Twenty-three studies had a cross-sectional design, whereas two had a pre- and posttest evaluation of education programs (Allert, Chalkley, Whitney, & Librett, 1997; Aved, Meyers, & Burma, 2007). All eligible articles were published in English.
Attitudes, Awareness, Behavior, and Group Differences Regarding Mandatory Reporting of IPV.
Note. IPV = intimate partner violence.
aBias estimate range 0–10: 0–3 = high risk of bias; 4–6 = moderate risk of bias; 7–10 = low risk of bias (Hoy et al., 2012). bBias estimate range 0–32 (Tong et al., 2007).
Sample sizes ranged from 24, in a qualitative study (Antle et al., 2010), to 3,455 (Glass, Dearwater, & Campbell, 2001). The smallest sample size in a quantitative study was 39 (Lund, 1999). In 16 studies, the population was female victims of IPV, and, in 8 of these, victims of IPV were compared to other female patient groups or other control groups. In 8 studies, the population was professionals: emergency department personnel; dental professionals; family, internal medicine, and obstetrics/gynecology doctors; paramedics; nurses; psychologists; or social workers. In one study, the population was police or sheriff responding to reports of IPV injuries from health practitioners (Lund, 1999). Race was reported in 15 studies, ranging from 20% (Malecha et al., 2000) to 83% White (Jordan & Pritchard, 2018). One of these 15 studies consisted of professionals (Rodriguez et al., 1999). Age was reported in 15 studies. Mean age of the participants ranged from 28.1 years (Cho et al., 2015) to 49 years (Feddock, Pursley, O’Brien, Griffith, & Wilson, 2009). One of these 15 studies consisted of professionals (Rodriguez et al., 1999).
Risk of Bias Within Studies
Bias and study limitations for quantitative studies were assessed at the outcome level by Hoy et al. (2012) Online Appendix 1: Risk of Bias Tool and for Qualitative Studies by Tong et al. (2007) Online Appendix 2: COREQ studies (Table 2). The results showed that the average measure reliability of Intraclass correlation (ICC) for two raters assessing 23 research (quantitative) studies was very high (ICC = .918, 95% confidence interval [.807, .965]). The average bias was moderate (M = 3.783); 1 study (4.3%; Sawyer et al., 2014) had low bias, 14 studies (60.9%) had moderate bias, and 8 studies (34.8%) had high bias. Seven studies indicated errors in the calculation and/or reporting of the numerator and/or denominator (Hoy et al., 2012; Table 2). The two qualitative studies (Antle et al., 2010; Rodriguez et al., 1998) obtained a score of 12 and 11 of a maximum score of 32, respectively (Tong et al., 2007).
Regarding measures of attitudes toward mandatory reporting, none of the studies used specific instruments to identify attitudes. All studies used questionnaires developed specifically for that study. None of the studies reported interrater reliability for the questionnaire tools. Attitudes were measured by items like the following: What do you feel/think/believe, view yourself as? Would it be more/less likely? Your opinion about, when, if ever, doctors should report? Would it prevent you from telling if mandatory reporting? Do you agree or disagree? Which one do you think is better? Should you have the right to, or would you have prevented? and the presentation of cases. Measures of attitudes toward mandatory reporting of IPV ranged from 1 single item (Feddock et al., 2009; Rodriguez et al., 2001; Sawyer et al., 2014) to 16 items (A. Smith & Parsons Winokur, 2004). However, some studies reported the number of items; others, the number of variables. Finally, conflating two or more mandatory policies (reporting, screening, arrest, no drop) in a study might affect the results (Gielen et al., 2000; Glass et al., 2001; A. Smith, 2000, 2001).
Results of Individual Studies
For presentation of all outcomes, see Table 2.
Synthesis of Results
This systematic literature review about mandatory reporting of IPV indicated, first, that IPV victims were generally supportive of the law that professionals should be required to report IPV. However, subsamples’ attitudes opposing mandatory reporting were presented as main findings in a substantial number of studies. Second, group differences between abused and nonabused women were mixed. Some studies found significant group differences regarding attitudes to mandatory reporting and consequences in help-seeking if mandatory reporting (e.g., current abuse, ethnicity, language, age, marital status, employment status, having children, multiple abusive relations, called the police, severity and frequency of IPV); others did not. In addition, some of the studies reporting group differences conducted analyses that included dependent variables. Third, knowledge about mandatory reporting of IPV among professionals was mixed and inconclusive. There were indications of group differences among professional disciplines and gender regarding compliance with mandatory reporting of IPV. Fourth, very few professionals had actually reported IPV under mandatory reporting. Fifth, none of the included studies investigated perpetrators’ attitudes to mandatory reporting of IPV. Finally, empirical research appears to be scarce, with moderate to high degree of bias and with only limited recent development: Six studies within the last 10 years, 2008–2019.
Victims’ attitudes to mandatory reporting of IPV
Four studies did statistical testing of the attitudes of abused versus nonabused women toward mandatory reporting of IPV. Two found a significant association (Feddock et al., 2009; Sachs et al., 2002); two did not (Gielen et al., 2000; Rodriguez et al., 2001). However, none of the studies that found significant differences conducted analyses adjusting for other group differences. Gielen et al. (2000), who conducted logistic regression analyses, did not find significant group differences.
Of the 15 studies that compared samples either supporting or opposing mandatory reporting, 8 found significant differences. Five of the 15 studies conducted logistic regression (Jordan & Pritchard, 2018; Rodriguez et al., 2001, 2002; Sachs et al., 2002; A. Smith & Parsons Winokur, 2004). Predictors of support were (1) non-White, (2) nonsingle, (3) had called the police during most recent victimization, (4) had been in multiple abusive relationships, (5) had children, and (6) extensive history of physical IPV (several incidents). Predictors of nonsupport were (1) living with perpetrator, (2) non-English speaker, (3) partner was employed, (4) Latina, (5) current IPV/IPV within the last year, and (6) prior history of IPV. Seven of the 15 studies were limited to descriptive analyses and results such as prevalence measured by %.
Professionals’ awareness, behavior, and attitudes to mandatory reporting of IPV
Nine studies conducted statistical testing of professionals’ awareness, behaviors, and attitudes. Two of these were evaluations of trainee programs for emergency department staff, prehospital care providers, and dental professionals (Allert et al., 1997; Aved et al., 2007). These studies found a significant increase of awareness and changing attitudes regarding mandatory reporting of IPV. Six studies did statistical testing of knowledge/awareness of mandatory reporting. Two of the six studies found significant results. However, neither of these two studies had conducted multivariate analyses. Three studies did statistical testing regarding professionals’ attitudes to mandatory reporting. Two studies had conducted logistic regression (Rodriguez et al., 1999; Tilden et al., 1994). One study found that primary care physicians reported lower compliance than other specialties (Rodriguez et al., 1999). However, education was not found to make a difference (Tilden et al., 1994). Eight studies did statistical testing of mandatory reporting behavior. Two studies found significant differences. However, none of these studies had conducted multivariate analyses. Only one descriptive study investigated whether the police/sheriff had standard procedures in place for responding to reports of IPV from health practitioners (Lund, 1999).
Risk of Bias Across Studies
Use of standard case definitions, of supporting or opposing mandatory reporting of IPV and awareness of mandatory reporting laws, is a key factor needed to ensure that information is collected in a systematic fashion. There were no explicit, uniform operational definitions of support for or opposition to mandatory reporting, nor of awareness of mandatory reporting laws. The risk of bias increased when all measurement scales and interview guides on mandatory reporting had been developed by the authors and not adequately validated prior to the investigation (Fellmeth, Heffernan, Nurse, Habibula, & Sethi, 2013). In addition, some measurements implied authors were having predefined values/attitudes about mandatory reporting in studies of help seekers: When, if ever, should doctors report? Would it prevent you from telling if doctors have mandatory reporting? If you knew in advance that your case would be reported, would you be less likely? Should you have the right to? Would you have prevented? The majority of studies had an acceptable sample size for the conducted analyses (Table 1). Only 36% of the studies conducted multivariate statistical testing. With descriptive and bivariate testing, it is not known if the group differences are significant or remain significant when adjusted for other group differences. Language bias arises because studies with statistically significant results conducted in non-English-speaking countries may be more likely to be published in English-language journals than those with nonsignificant results. Thus, as this review only reported on studies in English, our analysis may be based on fewer data.
Discussion
Summary of Evidence
Supporting versus opposing mandatory reporting
The most striking finding of this review is the scarcity of scientific research on mandatory reporting of IPV. The evidence on this issue is more limited than that on other efforts to prevent IPV. Even though WHO (2013) advised against mandatory reporting of IPV for clinicians and researchers, there has been limited scientific assessment of this practice to support this view. Although concerns are raised about mandatory reporting undermining victim autonomy (WHO, 2013) and reducing help-seeking, the included studies indicated victims generally were supportive of the law that professionals should be required to report IPV. Studies with results indicating abused women were less supportive of mandatory reporting were descriptive studies that did not adjust or control for other group differences between abused and nonabused women (Feddock et al., 2009; Sachs et al., 2002).
Awareness, attitudes, and behavior
The results of this review indicate that very few professionals or IPV victims have experiences with mandatory reporting of IPV, and several studies investigated awareness and attitudes toward it in populations that had no experience with it. Our results also indicate a moderate to high degree of bias within and across studies as well as limited recent research development on this topic. Above all, in several studies, we found indications of attitudes opposed to mandatory reporting among the researchers themselves: that is, systematic reporting of the statistical minorities who opposed mandatory reporting as being more significant than the statistical majorities who supported it, as well as interpreting the mandatory reporting laws as the major or only barrier to IPV help-seeking (Coulter & Chez, 1997; Jordan & Pritchard, 2018). Even analyses including dependent variables in the tested models were published as significant results (Jordan & Pritchard, 2018).
Women who supported mandatory reporting were more likely to discuss IPV with shelters or therapists whether there was mandatory reporting than women who were opposed to it. However, there were a few studies conducting multivariate analyses, controlling for group differences, that found significant contextual, sociodemographic, and IPV characteristics related to supporting versus opposing mandatory reporting of IPV (Rodriguez et al., 2001, 2002; Sachs et al., 2002; A. Smith & Parsons Winokur, 2004; Table 2). Some of these studies mixed dependent and independent variables in the models (Jordan & Pritchard, 2018; Sachs et al., 2002).
Pre- and posttests of professionals participating in courses indicated changes in awareness (Allert et al., 1997; Cho et al., 2015), but no changes in practicing mandatory reporting of IPV were measured. Similarly, studies of professionals asked about attitudes and awareness without including experiences with mandatory reporting (Allert et al., 1997; Aved et al., 2007; Cho et al., 2015; Rodriguez et al., 1999; Sawyer et al., 2014; Tilden et al., 1994). Some studies that included experiences with mandatory reporting of IPV indicated prevalence <10% (Aved et al., 2007; Cho et al., 2015; McDowell, Kassebaum, & Fryer, 1994). However, two studies found that 20–40% had reported abuse (Allert et al., 1997; J. S. Smith, Rainey, Smith, Alamres, & Grogg, 2008). The gap between attitudes and experiences might contribute to a vulnerable group not getting optimal and evidence-based treatment and risk assessment. Few studies measured professionals’ compliance with mandatory reporting laws (Rodriguez et al., 1999) or whether professionals regarded mandatory reporting as an appropriate intervention (Aved et al., 2007; Tilden et al., 1994). Moreover, the gap between victim support for mandatory reporting and limited professional experience or compliance with reporting might result in IPV victims not receiving the professional assistance they prefer.
Limitations
We may have missed studies of interest if they are not properly registered in the data bases by the search words we used. In addition, studies may have been overlooked if they have been published in less renowned journals, do not have the format of a scientific article, or are not published in the English or Scandinavian languages. The limited number of studies of mandatory reporting of IPV and the absence of the use of similar measurement tools in these investigations preclude making firm conclusions about patients’, abused women’s, women’s, or professionals’ attitudes, behaviors, or awareness of mandatory reporting of IPV. Furthermore, the suggested group differences and factors are far from establishing causal relationships. Finally, differences in the relevant legislation make comparisons across studies and countries difficult. The findings in this review offer no valid evidence for a major attitude, awareness, or behavior regarding mandatory reporting of IPV.
Most research still targets female victims, the main argument being that females suffer more severe consequences (Coker et al., 2002; Hines & Douglas, 2009) and seek help more frequently than male IPV victims. Only one study that included male patients was found (Houry, Feldhaus, Thorson, & Abbott, 1999), and no studies pertaining to perpetrators’ attitudes toward mandatory reporting of IPV were found in the search. There is no empirical evidence for generalizing to male victims or perpetrators of IPV from the current study.
Conclusions
Even though mandatory reporting of IPV was intended as a means of enhancing victims’ safety, preventing future violence, and improving the involvement of law enforcement and the criminal justice response, it has become a controversial issue. In this systematic literature review, we found 25 studies that investigated mandatory reporting of IPV. Our results indicated moderate to high degree of bias, and recent years have seen an increase neither in the number of research publications on mandatory reporting of IPV nor in the quality of empirical research. However, the WHO concluded that mandatory reporting of IPV by health-care providers is not recommended. The findings of our review did not provide empirical evidence supporting this advice. On the contrary, the results from the highest quality studies contradicted the WHO recommendation. If our findings are supported by further research, a vulnerable group might not achieve optimal and evidence-based treatment and risk assessment. Above all, we found some indications of attitudes opposing mandatory reporting among the researchers in several studies—that is, their systematically reporting findings of statistical minorities who opposed mandatory reporting as being more significant than those of statistical majorities who supported mandatory reporting of IPV, as well as mandatory reporting laws being the major or only barrier to IPV help-seeking. The gap between (1) strong attitudes, (2) limited awareness, and (3) scarce experience of mandatory reporting of IPV among professionals needs further investigation.
Summary of Critical Findings
Empirical research appears to be scarce with moderate to high degree of bias and few recent studies.
Victims were generally supportive of mandatory reporting laws. In spite of this, subsamples’ attitudes opposing mandatory reporting were presented as main findings in a substantial number of studies. Findings of group differences for attitudes between abused and nonabused women were inconclusive.
Knowledge about mandatory reporting of IPV among professionals was mixed and inconclusive. There were indications of group differences between professional disciplines and gender regarding compliance concerning mandatory reporting of IPV. Very few professionals had experiences with mandatory reporting of IPV.
None of the included studies investigated perpetrators’ attitudes to mandatory reporting of IPV.
Implications of Research, Practice, and Policy
Research
More empirical research is needed to ascertain whether mandatory reporting of IPV enhances victim safety and improves law enforcement.
Uniform operational definitions of supporting/opposing mandatory reporting and validated instruments are prerequisites for reliable and valid findings.
Practice
The gap between victim support of mandatory reporting and limited professional experience or compliance with reporting might result in IPV victims not receiving the professional assistance they prefer.
Policy
The findings in this review offer no valid evidence for the existence of a dominant attitude, awareness, or behavior regarding mandatory reporting of IPV.
Policy makers should put mandatory reporting on the educational agenda for the organizations that have professionals who are confronted with this challenge.
Supplemental Material
Supplemental Material, Appendix_2_Tong_2007 - Mandatory Reporting of Intimate Partner Violence: A Mixed Methods Systematic Review
Supplemental Material, Appendix_2_Tong_2007 for Mandatory Reporting of Intimate Partner Violence: A Mixed Methods Systematic Review by Solveig Karin Bø Vatnar, Kjartan Leer-Salvesen and Stål Bjørkly in Trauma, Violence, & Abuse
Supplemental Material
Supplemental Material, Hoy_et_al_2012_risk_of_bias_prevalence - Mandatory Reporting of Intimate Partner Violence: A Mixed Methods Systematic Review
Supplemental Material, Hoy_et_al_2012_risk_of_bias_prevalence for Mandatory Reporting of Intimate Partner Violence: A Mixed Methods Systematic Review by Solveig Karin Bø Vatnar, Kjartan Leer-Salvesen and Stål Bjørkly in Trauma, Violence, & Abuse
Footnotes
Acknowledgment
Acknowledgment is due to the skilled librarian of Oslo University Hospital, Norway, Marie Susannah Isachsen, for valuable help in the database search.
Declaration of Conflicting Interests
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding
The author(s) received no financial support for the research, authorship, and/or publication of this article.
Supplemental Material
Supplemental material for this article is available online.
References
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