Before Zimbabwe Breaks What Exists, It Must Answer One Question: What Happens to the Patient?

Potential conflicts of interest should be addressed. Governance standards should be strengthened. Related-party transactions should be transparent and independently audited.

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ZIMBABWE may be on the verge of one of the most consequential healthcare reforms in recent years.

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Yet before the proposed amendments to Statutory Instrument 330 of 2000 proceed, one uncomfortable question demands an answer:

What happens to patients if this experiment goes wrong?

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The proposed changes would prohibit medical aid societies from owning or operating healthcare facilities, effectively separating healthcare funders from healthcare providers. The objective is to address potential conflicts of interest and strengthen competition within the sector.

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At first glance, the principle is sound.

No healthcare system should tolerate practices that undermine patient welfare, distort markets or place institutional interests above those of the people it serves.

But healthcare policy cannot be designed around theory alone.

It must be tested against reality.

And Zimbabwe’s reality is stark.

Public hospitals remain under enormous pressure. Shortages of medicines and equipment persist. Healthcare workers continue to operate under difficult conditions. Medical aid coverage remains limited, and even those with medical aid often face substantial shortfalls and out-of-pocket expenses.

This is not a healthcare system with excess capacity.

It is a healthcare system with a shortage of capacity.

That is why the debate over SI 330 cannot simply be reduced to the question of whether vertically integrated healthcare models are theoretically desirable.

The more important question is whether dismantling them will improve the lives of patients.

Will healthcare become more affordable?

Will access expand?

Will quality improve?

Will families spend less out of their own pockets to obtain treatment?

If the answer is yes, the case for reform becomes compelling.

But if those outcomes cannot be demonstrated with evidence, then caution is justified.

At present, no publicly available evidence has been presented to show that vertically integrated healthcare facilities have, by their nature, caused widespread consumer harm in Zimbabwe.

If such evidence exists, it should be placed before the public.

If integrated models have restricted competition, undermined patient choice or inflated costs, then regulators not only have the authority to intervene—they have a duty to do so.

However, if the evidence remains inconclusive, policymakers should think carefully before implementing one of the most far-reaching structural changes the healthcare sector has seen in decades.

Because once capacity is dismantled, rebuilding it is neither quick nor easy.

If funder-owned facilities are removed from the system, where will the patients go?

Can public hospitals absorb the additional demand without longer waiting times and greater strain?

Will independent providers fill the gap?

If they do, what safeguards will prevent increased costs from being passed on to patients through higher tariffs, larger shortfalls and rising medical aid contributions?

These are not accusations against any stakeholder.

They are questions of public interest.

And they deserve answers.

None of this is an argument against reform.

Potential conflicts of interest should be addressed. Governance standards should be strengthened. Related-party transactions should be transparent and independently audited. Competition laws should be enforced. Pricing practices should be monitored. Abuse, where it exists, should be dealt with decisively.

But there is a profound difference between correcting weaknesses and dismantling existing capacity.

Good regulation fixes what is broken. It does not destroy what is functioning unless there is compelling evidence that patients will be better served as a result.

The burden of proof therefore rests with those advocating these amendments.

They must show, with evidence rather than assumption, that ordinary Zimbabweans will enjoy lower costs, better access and improved outcomes under the proposed system.

Healthcare policy should not be judged by how neatly it resolves theoretical conflicts on paper.

It should be judged by whether a grandmother gets her medication, whether a child sees a doctor in time and whether families can obtain treatment without financial ruin.

If Zimbabwe cannot yet say with confidence that these amendments will improve those outcomes, then the wiser course is not to abandon reform.

It is to pause, consult and refine it.

Because healthcare systems are far easier to dismantle than they are to rebuild.

And if this reform gets it wrong, it will not be institutions that suffer first.

It will be the ordinary Zimbabwean patient standing in a queue, searching for care that has become more expensive, more distant and harder to access.

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