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HEALTH CARE WORK AND INFORMATION SYSTEMS 51<br />

provide a mirror of medical work: they are tools used in doing the work. Patient<br />

records fulfil two, closely intertwined functions. First of all, they accumulate the<br />

data gathered during the course of a patient trajectory, resulting in the powerful<br />

‘external memory’ that a paper file provides. The progress notes, written down in<br />

chronological order by the professionals while they circulate through the shifts,<br />

afford the experienced reader a fast and efficient overview of the central key<br />

developments, actions and problems. Likewise, blood test results are<br />

accumulated in tables (generated by laboratory computers, or filled in by the<br />

ward secretary) that allow the reader to overview the patterns of increase and<br />

decrease in values through time, and to compare these fluctuations with the<br />

fluctuations apparent in other (blood) test results.<br />

The record’s accumulation function consists of two elements. First of all, it is<br />

obvious that the record is the place where data are gathered (where the data<br />

elements ‘accumulate’). Doctors, ward secretaries and nurses constantly write in<br />

the record, or paste notes or computer prints in it. Second, and less immediately<br />

obvious, the way the record organizes these data elements is important. The table<br />

with its built-in ease of comparison, and the progress form with its built-in<br />

chronology and standard headings add structure to the data entered: the data are<br />

put in a specific historical sequence, or in a specific context with other relevant<br />

blood test results. By collecting the data in this way, by providing for this<br />

specific sequence and context, the record’s form enhances the information<br />

content of these data: the blood test result becomes part and parcel of a whole<br />

array of data whose overall evolution is vastly more informative than each<br />

individual measurement. In pre-structured intake forms, for example, the pre-set<br />

headings of the intake form— ‘complaints’, ‘history’, ‘objective findings’,<br />

‘conclusion’ and ‘policy’ —suggest the classic reasoning process with which a<br />

doctor moves from ‘patient problem’ to ‘action plan’. Yet the order in which<br />

professionals enter bits and pieces of information on the form generally does not<br />

follow the temporal sequence suggested by the form. Part of the professional’s<br />

skill is to translate the patient’s stories and his actions into this neatly structured<br />

reasoning process, leading from ‘complaints’ through ‘objective findings’ to<br />

‘policy’. When such a form is re-read later, this implied and familiar reasoning<br />

process structures and speeds up the reading process, and the isolated data entries<br />

are interpreted in this framework. Even the paper forms in use in most current<br />

health care practices, then, can be said to process data. By structuring data entry,<br />

and by placing data elements in specific contexts and sequences, tables, progress<br />

forms and intake sheets make an important step in the transformation of the ‘raw<br />

data’ that is entered into ‘information’.<br />

In addition, through structuring and sequencing the work of professionals,<br />

PCISs coordinate activities and events at various locations and times. Standard<br />

headings on the progress notes structure the questions that physicians ask and the<br />

examinations that they perform, and make the notes of doctor A comparable to<br />

any other doctor using this form. Likewise, structured forms that are used by<br />

several people, at different moments (such as order-forms, checklists and so

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