0.00.51.01.52.0New Zealand adults who did not visit an after-hours medicalcentre because of lack of transport, at any point in the past 12 monthsBy gender, year ended June 2012–2020, % of adultsProvider: Ministry of Health201220132014201520162017201820192020MenWomen

New Zealand adults who did not visit an after-hours medical centre because of lack of transport, at any point in the past 12 months

By gender, year ended June 2012–2020, % of adults

Data calculation/treatment

All results presented in this data are weighted so that they are representative of the total population of adults 15+ and children aged 0–14 years (or a smaller subset where specified).
The dataset includes unadjusted prevalence figures for most indicators, estimated number of people, and 95% confidence intervals.
Indicators are provided by age group, gender, ethnic group (total response ethnicity, ie where people who belong to more than one ethnic group are counted once in each of the ethnic groups they identify with) and neighbourhood deprivation (area-based measure of socioeconomic position or deprivation, NZDep2018). Quintile 1 represents the 20 percent of areas with the lowest levels of deprivation and quintile 5 represents the 20 percent of areas with the highest level of deprivation.

The question about sexual identity was asked using a computer-assisted self-interview (CASI). It was not asked of respondents who were completing the interview with cognitive or language assistance from a family member/caregiver/friend. This was to ensure that no-one other than the interviewer/professional translator could hear the answers. However, there's still a chance that some respondents may not feel comfortable to answer truthfully.
Respondents also have the option of answering ‘don‘t know’ or choosing not to answer. Please note that a high level of item non-response was present for this question (3.7% in 2019/2020). Non-responses are excluded when calculating percentages or estimates of the population.

Disability status: The question set used to identify disabled people is known as the Washington Group Short Set (WGSS). The major objective of the Washington Group (WG) is to provide information on disability that is comparable throughout the world. The six domains included in the WGSS were chosen because they were found to be the ones that identified a majority of people at risk of being restricted in their independent participation in society. Using the WGSS, disabled people are those who have at least a lot of difficulty seeing or hearing (even with glasses or hearing aids), walking or climbing stairs, remembering or concentrating, self-care, or communicating.
The WGSS should not be used to produce estimates of disability prevalence or to investigate levels of need for services or environmental change. To meet these and other data needs, a disability-specific survey, with a more extensive question set, would be required. The population identified as disabled using the WGSS is considerably smaller than the population identified by disability-specific surveys. One of the limitations is that no WGSS question fully captures mental health impairments. The number of children in each year of the Health Survey who were identified as disabled by the Washington Group Short Set is too small to allow robust conclusions to be drawn so the results for children by disability status have not been shown.

For more information

https://minhealthnz.shinyapps.io/nz-health-survey-2019-20-annual-data-explorer/_w_d73d5508/#!/methodology

Limitations of the data

On 19 March 2020 the interviewing for the New Zealand Health Survey was suspended to reduce any risks of transmitting COVID-19 between interviewers and respondents. The 2019/20 Annual Explorer does not include any data collected since the COVID-19 Alert System was introduced by the Government in March 2020 to manage and minimise the risk of COVID-19 in New Zealand. It therefore does not include any information about people's health during the pandemic. The survey results for the 2019/20 New Zealand Health Survey are based on the data collected in the first three quarters of the year only. No adjustments or imputations have been done to account for the impact this has had on the 2019/20 data. This results in reduced sample sizes and in some cases, lower precision of the estimates. The majority of the adult and child indicators are not subject to any seasonal variation, and so are not impacted by the loss of data from one quarter of data collection.

The survey results are likely to underestimate or overestimate some indicators due to the nature of self-reported information. For example, many of the survey results assume that the respondents could accurately recall previous events (such as a diagnosis by a doctor). Also, many indicators are about diagnosed conditions, and not everyone with a particular condition will have had it diagnosed by a doctor. The amount of error will vary from indicator to indicator, depending on a number of factors, including the respondent’s age. Respondents may also over-report good behaviours or under-report risk behaviours based on what they consider to be socially desirable.

Some indicators (body size and raised blood pressure) are based on actual measurements taken by the surveyors rather than self-reported information. These results are more reliable than self-reported information because the surveyors apply consistent measurement techniques to all respondents using standardised measuring tools.

This survey presents a snapshot of the health of New Zealand adults and children at one point in time. The survey can be used to look at associations between different factors, such as health status and neighbourhood deprivation. However, we cannot conclude that the survey results show cause-and-effect relationships between these factors, in part because we do not know which factor occurred first. For example, if the survey finds that a particular condition is more common in people living in deprived areas, an association has been identified. This association does not necessarily mean the condition is caused by living in deprived areas.

Exclusions

Not included in the survey were: people living in institutions (such as for long-term hospital care, hospital- and dementia-level care in aged-care facilities, and in prisons), the homeless, short-term visitors and tourists.

Changes to data collection/processing

The 2019/20 results refer to the sample selected for the period July 2019 to March 2020. In other years, the results refer to the sample selected for the period July one year to June the next. No adjustments or imputations have been done to account for the impact this has had on the 2019/20 data.

Data provided by

Ministry of Health

Dataset name

New Zealand Health Survey: Prevalence/mean 2020

Webpage:

https://minhealthnz.shinyapps.io/nz-health-survey-2019-20-annual-data-explorer/_w_d73d5508/#!/download-data-sets

How to find the data

At URL provided, select the 'Download datasets' tab, and download the Prevalence/mean CSV file.

Import & extraction details

File as imported: New Zealand Health Survey: Prevalence/mean 2020

From the dataset New Zealand Health Survey: Prevalence/mean 2020, this data was extracted:

  • Rows: 2-14,703
  • Columns: 6-14
  • Provided: 132,318 data points

This data forms the table Health - All indicators of adults health (prevalence) 2007–2020.

Dataset originally released on:

November 19, 2020

About this dataset

The data provides a snapshot of the health of New Zealanders through the publication of key indicators on health behaviours, health status and access to health care for both adults and children.

Method of collection/Data provider

The New Zealand Health Survey (NZHS) conducts face-to-face interviews with adults and the parents/caregivers of children annually. The survey results refer to the usually resident population of all ages living in permanent dwellings, aged-care facilities and student accommodation.